Antimicrobial Properties of Capsaicin: Available Data and Future Research Perspectives
,1,2,† ,1,2,3,† ,3,4,* ,5,6 ,1 ,7,8 ,1,9,* and 1,10
Aristodemos-Theodoros Periferakis
1Department of Physiology, The “Carol Davila” University of Medicine and Pharmacy, 050474 Bucharest, Romania
2Elkyda, Research & Education Centre of Charismatheia, 17675 Athens, Greece
Argyrios Periferakis
1Department of Physiology, The “Carol Davila” University of Medicine and Pharmacy, 050474 Bucharest, Romania
2Elkyda, Research & Education Centre of Charismatheia, 17675 Athens, Greece
3Akadimia of Ancient Greek and Traditional Chinese Medicine, 16675 Athens, Greece
Konstantinos Periferakis
3Akadimia of Ancient Greek and Traditional Chinese Medicine, 16675 Athens, Greece
4Pan-Hellenic Organization of Educational Programs (P.O.E.P), 17236 Athens, Greece
Ana Caruntu
5Department of Oral and Maxillofacial Surgery, “Carol Davila” Central Military Emergency Hospital, 010825 Bucharest, Romania
6Department of Oral and Maxillofacial Surgery, Faculty of Dental Medicine, “Titu Maiorescu” University, 031593 Bucharest, Romania
Ioana Anca Badarau
1Department of Physiology, The “Carol Davila” University of Medicine and Pharmacy, 050474 Bucharest, Romania
Ilinca Savulescu-Fiedler
7Department of Internal Medicine and Cardiology, Coltea Clinical Hospital, 030167 Bucharest, Romania
8Department of Internal Medicine, The “Carol Davila” University of Medicine and Pharmacy, 050474 Bucharest, Romania
Cristian Scheau
1Department of Physiology, The “Carol Davila” University of Medicine and Pharmacy, 050474 Bucharest, Romania
9Department
of Radiology and Medical Imaging, “Foisor” Clinical Hospital of
Orthopaedics, Traumatology and Osteoarticular TB, 021382 Bucharest,
Romania
Constantin Caruntu
1Department of Physiology, The “Carol Davila” University of Medicine and Pharmacy, 050474 Bucharest, Romania
10Department
of Dermatology, ‘Prof. N.C. Paulescu’ National Institute of Diabetes,
Nutrition and Metabolic Diseases, 011233 Bucharest, Romania
Kai Wang, Academic Editor
1Department of Physiology, The “Carol Davila” University of Medicine and Pharmacy, 050474 Bucharest, Romania
2Elkyda, Research & Education Centre of Charismatheia, 17675 Athens, Greece
3Akadimia of Ancient Greek and Traditional Chinese Medicine, 16675 Athens, Greece
4Pan-Hellenic Organization of Educational Programs (P.O.E.P), 17236 Athens, Greece
5Department of Oral and Maxillofacial Surgery, “Carol Davila” Central Military Emergency Hospital, 010825 Bucharest, Romania
6Department of Oral and Maxillofacial Surgery, Faculty of Dental Medicine, “Titu Maiorescu” University, 031593 Bucharest, Romania
7Department of Internal Medicine and Cardiology, Coltea Clinical Hospital, 030167 Bucharest, Romania
8Department of Internal Medicine, The “Carol Davila” University of Medicine and Pharmacy, 050474 Bucharest, Romania
9Department
of Radiology and Medical Imaging, “Foisor” Clinical Hospital of
Orthopaedics, Traumatology and Osteoarticular TB, 021382 Bucharest,
Romania
10Department
of Dermatology, ‘Prof. N.C. Paulescu’ National Institute of Diabetes,
Nutrition and Metabolic Diseases, 011233 Bucharest, Romania
†These authors contributed equally to this work.
Received 2023 Aug 26; Revised 2023 Sep 13; Accepted 2023 Sep 20.
Abstract
Capsaicin
is a phytochemical derived from plants of the genus Capsicum and
subject of intensive phytochemical research due to its numerous
physiological and therapeutical effects, including its important
antimicrobial properties. Depending on the concentration and the strain
of the bacterium, capsaicin can exert either bacteriostatic or even
bactericidal effects against a wide range of both Gram-positive and
Gram-negative bacteria, while in certain cases it can reduce their
pathogenicity by a variety of mechanisms such as mitigating the release
of toxins or inhibiting biofilm formation. Likewise, capsaicin has been
shown to be effective against fungal pathogens, particularly Candida spp., where it once again interferes with biofilm formation. The parasites Toxoplasma gondi and Trypanosoma cruzi
have been found to be susceptible to the action of this compound too
while there are also viruses whose invasiveness is significantly
dampened by it. Among the most encouraging findings are the prospects
for future development, especially using new formulations and drug
delivery mechanisms. Finally, the influence of capsaicin in somatostatin
and substance P secretion and action, offers an interesting array of
possibilities given that these physiologically secreted compounds
modulate inflammation and immune response to a significant extent.
Keywords: capsaicin, antibacterial actions, antifungal actions, antiparasitic actions, antiviral actions
1. Introduction
Antimicrobial
resistance is an emerging threat identified by the World Health
Organization and represents a global concern due to newly-acquired
resistance mechanisms in a multitude of pathogens [1].
Antimicrobial drugs misuse as well as clinical and non-clinical
pathogen transmission have contributed to the development of
antimicrobial resistance, therefore novel antimicrobials are actively
researched to combat this menace [2].
In
the last decades there has been an increasing interest in the
development of new antimicrobial substances from plants, as evidenced by
a multitude of research on the subject (e.g., [3,4,5,6,7,8,9,10,11,12,13,14,15,16]).
This renewed interest is based on the long-standing medical practices
of various traditional medical systems, where plants and their derived
extracts have been reported to have a host of applications. One
important such substance is capsaicin, a chemical compound derived from
plants of the Capsicum species [17].
Capsaicin (8-methyl-N-vanillyl-6-nonenamide) is a nitrogen-containing substance belonging to the lipids group [18]. While capsaicin was a term originally used to refer to a host of compounds isolated from C. oleoresin, nowadays it is a substance-specific name, while the rest of the originally associated substances are called capsaicinoids [19].
When isolated in its pure form, capsaicin (C18H27NO3) is a solid, colourless, hydrophobic, highly volatile, and highly pungent substance [20], which will produce toxic fumes if heated to decomposition levels [21]. The naturally occurring form of capsaicin is its trans form [22]. The biosynthetic pathway of capsaicin was originally described in the 1960s [23,24,25,26]. A number of methods to artificially synthesize capsaicin have been described [27].
Based on its properties, capsaicin is already used in a number of applications, as a component of animal repellents [28,29,30], fragrances [31,32], pesticides [33,34], and also in veterinary medicine [35,36]. A number of medical uses were reported, most notably as a treatment for chronic pain [37,38,39,40] and pruritus [41,42,43,44]; other minor uses have also been described by various researchers [45,46,47,48,49,50,51,52]. It should be noted that capsaicin is also capable of inducing local inflammation [53], a process which can be objectively measured through modern imaging applications [54,55].
In
this paper, we will present a thorough and representative view of the
studies regarding the actions and effects of capsaicin against bacteria,
fungi, protozoa, and viruses. For this review, we carried an
exploratory search using the Pubmed database from the National Center
for Biotechnology Information (NCBI) of the United States of America
(available at https://pubmed.ncbi.nlm.nih.gov/;
accessed on 25 August 2023) which includes over 36 million citations
for the biomedical literature from MEDLINE as well as other scientific
sources. We used “capsaicin”, “antimicrobial action”, “antibacterial”,
“antifungal”, “antiviral”, and “antiparasitic” as keywords, and included
all relevant papers on the topic. We further supplemented the search in
other databases such Google Scholar and Scopus. For each pathogen, we
presented its relative importance in a clear and comprehensive way,
based on current clinical evidence. By also describing the molecular
mechanisms underlying the antimicrobial effects of capsaicin, we hope to
depict a complete picture of the current corpus of knowledge on the
subject and point out promising future research perspectives including
the need to develop and test new capsaicin formulations.
2. Antibacterial Properties of Capsaicin
In
the last decades, the use of plant metabolites against bacteria has
been on the foreground of phytomedical and microbiological research
(e.g., [56,57,58,59,60,61]). Capsaicin in particular has been the focus of recent research as a potential solution against antibiotic resistance [62].
Apart from finding natural alternatives to antibiotics, this is
important both for those patients in which some antibiotics may be
toxic—typical examples include allergies [63,64,65], liver toxicity [66,67,68,69], and other side effects [70]—and also, and perhaps more significantly, due to the increasing antibiotic resistance [71,72,73,74,75,76,77]. The rapid increase in antibiotic resistance is mainly explained by the overuse of antibiotics [78,79,80]
and the high adaptability of bacteria in general, which may survive,
depending on the species, even in extreme environments such as hot
springs (e.g., [81,82,83]). The research on the antibacterial properties of capsaicin is extensive ()
and this leaves open many potential choices for new drug design.
Minimum inhibitory concentration (MIC) represents the lowest
concentration of an antibacterial agent which, under in vitro
conditions, totally prevents the visible growth in the tested strain [84].
Assessing this value is relevant to ensure the effectiveness of the
antibiotic substance while limiting its administration to prevent
adverse effects.
Table 1
Antibacterial actions of capsaicin based on existing research.
Genus | Species | Extract from | MIC (μg/mL) | Year of Research | Reference |
---|
Gram Positive |
Staphylococcus |
S. aureus
|
Capsicum frutescens
| 1.2 | 2014 | [85] |
Capsicum chinense
| not specified | 2018 | [86] |
Streptococcus |
S. pyogenes
| Capsicum spp. | 64–128 | 2015 | [87] |
Enterococcus |
E. faecalis
|
Capsicum frutescens
| 25 | 2014 | [85] |
Bacillus |
B. subtillis
|
Capsicum frutescens
| 25 | 2014 | [85] |
Listeria |
L. monocytogenes
| Capsicum spp. | not specified | 2018 | [88] |
Gram Negative |
Vibrio |
V. cholerae
| Capsicum spp. | 100 | 2010 | [89] |
Acinetobacter |
A. baumanii
| Capsicum annuum L. | 64 | 2011 | [90] |
Helicobacter |
H. pylori
| Capsicum spp. | 25 | 2005 | [91] |
Salmonella |
S. typhimurium
|
Capsicum chinense
| not specified | 2022 | [92] |
Escherichia |
E. coli
|
Capsicum frutescens
| 5 | 2014 | [85] |
Capsicum chinese
| not specified | 2018 | [86] |
Klebsiella |
K. pneumoniae
|
Capsicum frutescens
| 0.6 | 2014 | [85] |
Proteus |
P. mirabilis
| Capsicum annuum L. | 32 | 2011 | [90] |
Pseudomonas |
P. aeruginosa
|
Capsicum frutescens
| 10 | 2014 | [85] |
Capsicum spp. | not specified | 2018 | [93] |
2.1. Antibacterial Activity against Staphylococcus aureus
Staphylococcus aureus is a bacterium that can frequently colonize the human body [94].
However, it is also known to cause a variety of diseases ranging from
food poisoning to infections of the skin, such as scalded skin syndrome [95], or in the most severe cases, pneumonia and bacterial endocarditis [96,97].
Its biochemical arsenal comprises many toxins such as its enterotoxin
and its exfoliative toxins, which are responsible for the aforementioned
food poisoning and skin infections, respectively, and its hemolysin,
called α-toxin [98]. Regarding the enterotoxin of S. aureus, it should also be mentioned that it is a super-antigen [98]. The emergence of Methicillin-resistant Staphylococcus aureus strains, also known as MRSA, is an important factor of concern both in a medical setting and from an economic point of view [99,100].
There are several types of MRSA such as the healthcare-associated MRSA
(HA-MRSA), the community-associated MRSA (CA-MRSA), and the
livestock-acquired MRSA (LA-MRSA) [101].
Capsaicin has potent action against S. aureus [102].
Specifically, it has been shown to affect the cellular viability of
staphylococcal cells, exhibiting partial to total bactericidal effects,
depending on the tested variety and the dilution level [88].
The extract of Bhut Jolokia Red is particularly potent in this regard,
exhibiting partial bactericidal action even at 1:16 dilution [88]. Other studies have concluded that the effects on the growth in S. aureus colonies are more pronounced in the variety Noga Bhut when compared with the variety Roja Bhut [86].
When tested on mice, evidence suggests that capsaicin can have a
protective role in staphylococcal pneumonia, as it was found to suppress
the production of α-toxin and alleviate the inflammatory reaction [103].
2.2. Antibacterial Activity against Group A Hemolytic Streptococci
Streptococcal infections are associated with several pathologies such as skin infections, pharyngitis, pneumonia [104,105], and a critical condition known as toxic shock syndrome (TSS) [98].
Furthermore, due to the nature of protein M, one of the bacterium’s
major antigens, virulence is high and reinfection with different M
strains is a possible occurrence [105,106,107].
Other important parts of this bacterium’s antigenic structure are its
pyrogenic toxin and its erythrogenic toxin, which are classified as
superantigens [108],
while it should also be mentioned that the species belonging to the
category of group A hemolytic streptococci, most notable of them being S. pyogenes, owe this trait of theirs to their hemolysin, streptolysin O [109].
Perhaps the most notable trait of Streptococcus are the so-called
post-streptococcal diseases, a group of severe sequelae which includes
glomerulonephritis, rheumatic fever, and rheumatic heart disease,
brought about due to different types of hypersensitivity reaction [104,106].
Macrolides, for example erythromycin, are becoming less and less
effective as resistant strains emerge, and this poses a problem in the
treatment of streptococcal infections in patients who are allergic to
β-lactam antibiotics to which the bacterium is still susceptible [87,106].
Capsaicin
was found in vitro to affect the biofilm formation and epithelial cell
adhesion of species belonging to Group A hemolytic streptococci,
reducing their invasiveness, while also having bactericidal action [87]. Moreover, the hemolytic activity of these species was diminished by a notable amount [87]. Apart from S. pyogenes, S. mutans has also been found to be susceptible to capsaicin [102].
2.3. Antimicrobial Activity against Enterococcus Species
The most notable species of enterococci are E. faecium and E. faecalis [110]. In recent years, enterococci have become the source of a considerable number of nosocomial infections [111] which can be of high severity [112,113].
The emergence of vancomycin-resistant enterococci (VRE) is a source of
concern which indicates that alternative treatment options should be
looked into [114].
Research results indicate that capsaicin can be used to inhibit the growth in E. faecalis, although it should be mentioned that its MIC was among the higher ones during the tests conducted by Nascimento et al. [85]. This can be possibly attributed to the fact that this bacterium, like others inhibited by similar MIC values, such as B. subtilis and P. aeruginosa, utilize capsaicin as a nutrient for growth [115].
However, dihydrocapsaicin exhibited lower MIC values than capsaicin in
the aforementioned study, while also presenting a selective bactericidal
effect related to cellular wall characteristics [85].
2.4. Antimicrobial Activity against Bacillus Species
Bacteria of the Bacillus genus are aerobic [116]
and have a characteristic spore-forming ability, becoming resistant to
the action of disinfectants as well as unfavourable environmental
conditions [117,118]. Most species of the Bacillus genus are not pathogenic, the most notable exceptions being B. anthracis and B. cereus which associate increased mortality [119].
B. subtilis
is non-pathogenic but the study of the action of capsaicin against it
could be beneficial in understanding the action mechanisms against the
aforementioned pathogenic species. Evidence from different sources [85,120] suggests that capsaicin is capable of inhibiting the growth in B. subtilis though at a comparatively higher MIC than most other bacteria [85]. Conversely, the species B. thuringiensis did not seem to be nearly as susceptible to the action of capsaicin [102]. Although B. thuringiensis is not pathogenic for humans, this finding may be of relevance, given the use of B. thuringiensis as a biopesticide [121].
2.5. Antimicrobial Activity against Listeria monocytogenes
Listeria monocytogenes
is a species of ubiquitous, intracellular bacteria responsible for
foodborne pathologies, capable of causing severe complications such as
meningoencephalitis, especially in risk groups like immunosuppressed
individuals, as well as pregnant women and foetuses, where abortion and
septic premature death/neonatal death can occur [122,123,124].
The bacterium owes its intracellular nature to a variety of factors,
most notably its internalins, which enable it to enter the host cell,
and its hemolysin, listeriolysin O, which enables it to escape
intracellular vacuoles [123].
The response of L. monocytogenes
when exposed to capsaicin varies in lab settings depending on the
extract with some displaying bactericidal action and others displaying
bacteriostatic action [88].
The extract of Bhut Jolokia Red seems to be among the most effective
ones, exhibiting partial bactericidal action even at 1:16 dilution [88].
2.6. Antimicrobial Activity against Vibrio cholerae
Vibrio cholerae
is the causative agent of one of the oldest diseases known to man,
characterized by profuse diarrhoea, which can be commonly found in
aquatic ecosystems [125,126]. There are several biotypes which have pathogenic properties, featuring a great number of virulence factors [127]. Resistant strains of Vibrio cholerae are causes of concern [128,129] necessitating the search for alternative methods of treatment.
Capsaicin
has been found to significantly reduce the release of cholera toxin by
interfering with the transcription of txA, tcpA, and toxT genes while at
the same time enhancing the transcription of the hns gene which, in
turn, downregulates the transcription of the former genes [89]. It should be mentioned that these results were noted along different serogroups and biotypes of this bacterium [89].
This is an important finding since several among them are responsible
for pandemics and, as previously mentioned, some have also developed
resistance to conventional antimicrobial agents [130].
2.7. Antimicrobial Activity against Acinetobacter baumanii
Acinetobacter baumannii is implicated in pulmonary infections and septicaemia in immunocompromised patients [131]. Its ability to resist the action of antibiotics and survive in harsh environments [132,133,134] only serves to exacerbate its pathologic nature. Based on the research of Ozçelik et al. [90], capsaicin is effective against A. baumannii at a concentration of 64 μg/mL. Interestingly, the research of Guo et al. [135]
showed a lack of direct action of capsaicin against colistin-resistant
strains of this bacterium but noted potent synergistic action in the
case of combinatory use of these substances in a dose-dependent manner,
where colistin MIC was greatly reduced.
2.8. Antimicrobial Activity against Helicobacter pylori
Helicobacter pylori
is a causative agent of gastric ulcer and gastric cancer that displays
increased rates of resistance to previously effective antibiotics such
as clarithromycin and, to a lesser extent, metronidazole [136]; it is often characterised by multi-drug resistance patterns [137].
Capsaicin has showed promising bacteriostatic results at in vitro testing [138].
Its effects are exerted at concentrations as low as 25 μG/mL with the
best results being achieved at 50 μG/mL, indicating possible use as a
treatment option [91]. The usefulness of capsaicin as a treatment option for H. pylori
also extends to the fact that it has demonstrated the ability to
downregulate the proinflammatory pathway NF-Kb when tested in vivo on
mice [139], a finding corroborated by other researchers [140], thereby reducing the extent of the inflammatory response caused by the bacterium and the subsequent gastric damage [139].
2.9. Antimicrobial Activity against Salmonella typhimurium
Salmonella
is a common causative agent of foodborne pathologies, which is mainly
found in poultry, eggs, and dairy products, that threatens public health
worldwide [141,142]. This bacterium displays a great serovariability with over 2600 serotypes having been recorded [143] and with different strains exhibiting different degrees of antigenic variability [144]. There are several strains which are resistant to the action of antibiotics [145,146] and their number is increasing at an alarming rate [147] while, at the same time, the increased virulence of said strains leads to a higher mortality [148].
Capsaicin has been documented as having partial bactericidal effects against Salmonella typhimurium [88]. Pure capsaicin exhibits protein-inhibiting qualities while extract from the plant Capsicum chinense (C. chinense) seems to be even more potent in that regard at the same doses while also preventing infection of Vero cells [92].
Based on the aforementioned data, future studies will hopefully
elaborate on the antibacterial actions of capsaicin against other
strains of the pathogenic Salmonella spp.
2.10. Antibacterial Activity against Escherichia coli
Escherichia coli
is a commensal bacterium found in the gastrointestinal tract which can
cause opportunistic infections if it migrates to different locations or
when the host becomes immune-suppressed [149]. There have been recorded different types of E. coli, namely the enteropathogenic E. coli (EPEC), the enterohemorrhagic E. coli (EHEC), the enterotoxigenic E. coli (ETEC), the enteroaggregative E. coli (EAEC), the enteroinvasive E. coli (EIEC), and the diffusely adherent E. coli (DAEC) [150]. The emergence of multi-drug resistant (MDR) E. coli poses a problem that must be addressed in alternative ways such as new antibacterial substances [151,152].
Capsaicin has been shown to have partial bactericidal effects on Escherichia coli O157:H7 [88]. The inhibitory nature of capsaicin against E. coli has been confirmed by another study [85] though other researchers’ findings indicate that capsaicin merely slows down its growth [120]. At any rate, the effects of capsaicin on E. coli colonies are more potent in the case of the variety Roja Bhut when compared with the variety Noga Bhut [86].
2.11. Antibacterial Activity against Klebsiella pneumoniae
Klebsiella pneumoniae
is an opportunistic pathogen which infects people worldwide, accounting
for one-third of the total Gram-negative bacterial infections [153], and poses a considerable threat particularly in the nosocomial environment [154] where it can cause severe pathologies [155].
Due to strains which are resistant to antibiotics, including even
last-line antibiotics, alternative methods of treatment are a necessity [154,156].
There is research evidence which suggests that capsaicin can exert an inhibitory effect on the growth in K. pneumoniae [85]. The usefulness of capsaicin’s action against K. pneumoniae is backed up by similar findings of other researchers [157].
Similarly, a formulation containing honey/tripolyphosphate/chitosan
nanofibers loaded with capsaicin and gold nanoparticles was found to
have inhibitory action against several bacteria, one of which was a
different strain of the bacterium in question called Klebsiella rhinoscleromatis [158].
2.12. Antimicrobial Activity against Proteus Species
Proteus mirabilis and Proteus vulgaris
are the most notable species of their genus and they are associated
with urinary tract infections, like cystitis and pyelonephritis, while
there have also been recorded cases of asymptomatic bacteriuria in
elderly patients as well as patients with type 2 diabetes [159,160,161]. Urinary stone formation [162] and catheter obstruction in catheterized patients [163] are also possible complications. The severity of the pathologies caused by the aforementioned bacteria can be very severe [162,164],
especially given the fact that there is a risk of these urinary stones
serving as a focal point for other bacterial infections [164]. Bacteria of the Proteus genus have grown resistant to the action of antibiotics [165,166] and there even exist some MDR Proteus strains [167,168,169,170]. P. vulgaris in particular has been implicated in resistant nosocomial infections [171].
Capsaicin is effective against P. mirabilis as shown by the research of Ozçelik et al. [90]. P. vulgaris
on the other hand has shown resistance to the effects exerted by
capsaicin in tandem with other substances, which was attributed to its
ability to elongate itself and secrete a polysaccharide when in contact
with surfaces [102].
2.13. Antimicrobial Activity against Pseudomonas Species
Pseudomonas aeruginosa
is a bacterium which can cause localized as well as systemic infections
which are at times mild but can reach life-threatening severity [172], and is also commonly associated with nosocomial infections [173]. Patients with cystic fibrosis and COPD in particular are a risk group for P. aeruginosa infections [174,175,176]. There are P. aeruginosa strains which are becoming resistant to the action of antibiotics, meaning that new treatment options must be sought [177,178].
Studies have demonstrated the inhibiting properties of capsaicin on the growth in P. aeruginosa
colonies even though the MIC is relatively high when compared to that
of the other bacterial species tested by Nascimento et al. [85]. Based on the research of Kushwaha et al. [93],
capsaicin along with 6-gingerol was able to inhibit the production of
rhamnolipids, phenazine, and quinolone among other compounds; this
finding may be important in dealing with resistant strains during
biofilm formation. Capsaicin has also been shown to slow down the growth
in a different species, Pseudomonas solanacearum [120].
3. Capsaicin as an Antifungal Agent
Compared to bacteria, only a limited fraction of fungi are considered to be pathogenic to humans [179]. While the majority of common fungal infections are not life-threatening, some species, such as Candida albicans and Aspergillus fumigatus,
can even cause life-threatening infections under specific
circumstances. While not as prominent as other pathogens, still they
represent a considerable threat [179] and the burden of disease is high at least in specific regions [180,181,182]. Resistance to antifungal drugs is also a matter of concern [183,184,185] as is their side effects in some cases [186,187,188].
The main focus of study for the antifungal effects of capsaicin has been two gena, Candida and Aspergillus (), which are among the most common human fungal pathogens.
Table 2
Antifungal actions of capsaicin based on existing research.
Genus | Species | Extract from | MIC (μg/mL) | Year of Research | Reference |
---|
Candida | C. albicans, C. glabrata, C. tropicalis |
Capsicum frutescens
| 25 (MIC100) | 2014 | [85] |
Capsicum chinense
| 187.5–1500 (MIC100) | 2022 | [189] |
Apsergillus |
A. parasiticus
|
Capsicum chinense
| 68 (MIC50) | 2020 | [190] |
381 (MIC50) | 2020 | [191] |
3.1. Antifungal Activity against Candida spp.
Candida spp. are usually benign but under certain circumstances, particularly in the case of Candida albicans, they can cause several pathologies, for example in the oral cavity [192] with many women also contracting vaginal candidiasis [193,194]. However, they have also been implicated in systemic infections of life-threatening severity [195]; this is dependent on the presence of risk factors [196,197]. Lately, the problem has become most evident in the hospital setting [198,199].
There has been extensive research on the susceptibility of Candida spp. to capsaicin, with satisfactory results. Capsaicin exhibits notable inhibiting properties against Candida albicans [85].
This inhibition becomes evident at 1:4 and 1:8 dilutions, with the
yeast cells being killed, while the potency of the researched extracts
was highlighted by the fact that all of them achieved partial inhibition
even at 1:16 and 1:32 dilutions [88]. Capsaicin has also been shown to reduce the mature biofilm of C. albicans by 70–89% [200].
It has been concluded that capsaicin exerts its effects on the yeast
cells by preventing ergosterol biosynthesis in the cell wall, thereby
altering their shape and compromising their integrity [200]. Other species of Candida, like C. glabrata and C. tropicalis, were even more susceptible than C. albicans
with not only their biomass formation being inhibited, but likewise the
former’s biofilm-formation capacity being greatly diminished [189]. Indicatively, the MIC of extracts from Capsicum chinense was 1500 μg/mL for C. albicans but only 187.5 μg/mL for C. glabrata [189]. The hemolysis produced was similarly reduced by a significant degree [189].
Another very important finding was the fact that the action of
fluconazole against yeast cells is enhanced when combined with
capsaicin, which means that there could be a viable way of preventing
the development of resistance to the aforementioned drug [200].
3.2. Antifungal Activity against Aspergillus parasiticus
The species of Aspergillus which are most relevant from a medical point of view are A. parasiticus and A. flavus, as they produce aflatoxins, secondary metabolites with harmful effects on both humans and animals [201], most notably carcinogenesis, mutagenesis, and teratogenesis [202].
Due to climate change, these species of Aspergillus can now be found in
the soil of many countries worldwide, including Europe [203,204]. Considering that the use of harmful synthetic insecticides is common practice for eliminating A. parasiticus, the need for more environment-friendly methods of eradication has emerged [205].
Nanoparticles containing capsaicin and chitosan were tested against A. parasiticus,
and the results were promising in that the incorporation of capsaicin
in chitosan-containing lipid nanoparticles maintained a good antifungal
effect while reducing the toxicity of the formulation [205]. Research results indicate that capsaicin not only has an inhibitory effect on the growth in A. parasiticus, but it also interferes with the germination of its spores and reduces the production of the aflatoxins [190,191] by suppressing the expression of the relevant genes aflM, aflR, aflS, and especially aflD [190]. This means that capsaicin-based compounds could be a useful source of non-synthetic fungicides [191].
4. Capsaicin as an Antiparasitic Agent
While most parasites are a danger to human health in the areas in which they are endemic [206,207,208], a host of factors may facilitate their spreading [209,210]. Thus, it may be imagined that the burden of disease is potentially considerable [211,212,213] and may increase given the emerging resistance [214,215]; even more so, some antiparasitic drugs, like antimonials, can have significant side effects [216]. Currently, the focus regarding the antiparasitic properties of capsaicin is centred on two species ().
Table 3
Antiparasitic actions of capsaicin based on existing research.
Genus | Species | Extract from | IC50 | Year of Research | Reference |
---|
Toxoplasma |
T. gondii
|
Capsicum chinense
| 42.12 µg/mL | 2022 | [189] |
Trypanosoma |
T. cruzi
| Capsicum spp. | 0.26–6.26 µM | 2020 | [217] |
4.1. Antiparasitic Activity against Toxoplasma gondii
Toxoplasma
is an obligate intracellular eukaryotic parasite with a great spread;
in fact, it is estimated that it infects up to one-third of the world’s
population [218,219]. Oftentimes, infections caused be this protozoon are mild or even asymptomatic [218,220].
Their severity can be life-threatening however in the case of
immunocompromised patients and newborns, the latter due to congenital
transmission [218,219,220]. Pathologies of the retina and of the central nervous system are the ones most commonly associated with this microorganism [218].
A particularly common problematic finding is the development of tissue
cysts which can lead to relapses in case of rupturing when a robust
immunity is not present [221,222]. The parasite has a complex life cycle with many forms, namely tachyzoites, bradyzoites, and sporozoites [221].
Regarding its vector, felines serve as its definitive host and the
oocysts developed within them are quite resistant when exposed to
environmental conditions [218]. Even though toxoplasma is highly antigenic [220], it has at its disposal many proteins that enable it to evade the defences of our immune system [218,219,220]. T. gondii
in particular uses specialized secretory proteins which allow it to
invade and replicate within the host cell by modifying some of the
latter’s factors [219]. This is achieved by means of interfering with gene transcription and signalling pathways [220].
Pyrimethamine and trimethoprim are the main treatment options but, due
to the fact that they cannot distinguish between the enzymes of the
parasite and the host, they should be administered together with
sulphonamides, most notably sulfadiazine [222]. The result is severe side effects and subsequently, lower compliance rates [222]. There are also mentions of drug-resistant T. gondii strains [223,224]. As such, searching for better alternatives is a medical necessity.
Research results have shown that T. gondii-
infected BeWo cells show inhibited proliferation when treated with
non-toxic concentrations of capsaicin in twofold serial dilutions, with
the half inhibitory concentration (IC50) against its tachyzoites being
42.12 μg/mL [189].
From a pharmacological point of view, combinatory use of pyrimethamine
and sulfadiazine alongside capsaicin yielded much better results than
both of the two drugs combined or capsaicin alone [189].
4.2. Antiparasitic Activity against Trypanosoma cruzi
The most notable species of Trypanosoma are T. brucei, T. gambiense and T. rhodesiense. The main associated pathology is sleeping sickness, a disease endemic to African countries [225]. Its vectors are the Glossina flies, without excluding transmission by other blood-sucking insects [226,227].
The drugs used for the treatment of this condition are of two
categories; the blood–brain barrier-crossing drugs, indicatively
melarsoprol, eflornithine and nifurtimox, and the non-blood–brain
barrier-crossing drugs like pentamidine and suramin [228]. Resistant strains are not prevalent but nor are they unheard of [229]. There is also T. cruzi, which is the causative agent of Chagas disease, which also has a zoonotic transmission [229].
T. cruzi was found to be susceptible to the action of capsaicin, with its trypomastigotes being affected more than its epimastigotes [217].
Although the research did not manage to find the exact target of
capsaicin, its efficacy is undeniable considering that it exerted its
effects in nanomolar concentrations with a potency many times higher
than benznidazole, the drug mainly used for treatment of Chagas disease [217].
Findings also suggested that a capsaicin-based treatment could have an
oral administration, another upside as far as therapeutical
considerations are concerned [217].
5. Capsaicin as an Antiviral Agent
There have been many studies in the last few years documenting the extensive burden of disease from common viral pathogens [230,231,232,233].
Given that for many of the most common viral pathogens, there is a
pattern of increasing resistance to antiviral drugs and recombinant
strains emergence [234,235,236,237,238,239], and many viruses are associated with severe persistent pathological features [240,241,242,243,244,245], the research on natural antiviral substances is ever more important.
The emergence of the coronavirus disease 2019 (COVID-19) [246,247]
highlighted that despite the important progress in antiviral medicines,
there are still significant gaps in our antiviral arsenal. Given the
existence of deadly viruses, which could be potential pandemic-inducing
agents, like the Marburg [248,249] and Ebola [250,251]
viruses, and the existence of other viruses where there is not any
fully effective therapeutical scheme, like the rabies virus [252,253],
the need for novel antiviral agents becomes ever more evident.
Unfortunately, comparatively little research has been undertaken in the
antiviral front, and at the moment, it can be certainly said that
capsaicin is definitively effective against only a limited number of
viral pathogens ().
Table 4
Antiviral actions of capsaicin based on existing research.
Family | Genus | Extract from | EC50 (μmol/L) | Year of Research | Reference |
---|
Orthomyxoviridae | Influenza | Capsicum spp. | n/a | 2022 | [254] |
Arenaviridae | Lassa | Capsicum spp. | From 6.1 to over 30 (strain-dependent) | 2020 | [255] |
5.1. Antiviral Activity against the Influenza Virus
The
influenza virus is a highly contagious virus that affects mainly the
respiratory system and is characterized by high antigenic variability
due to the genetic alterations it often undergoes [256,257,258]. This is true especially for type A influenza which is prone to causing pandemics [258].
Influenza’s antigenic variability comprises the antigenic shift and the
antigenic drift it exhibits, the former being the cause of the
aforementioned pandemics [259] and the latter necessitating constant updating of the vaccines [257].
A variety of medication is used for treatment, most notably the protein
M-inhibiting drugs amantadine and rimantadine, to which the virus is
now greatly resistant [260], the cap-dependent endonuclease-inhibiting drugs like baloxavir and marboxil [261,262], which can also be used for prophylactic purposes [263], and neuraminidase-inhibiting drugs like oseltamivir [257].
However, the available treatment loses a considerable part of its
efficacy if it is not administered within the first stages of the
infection, with the first 24 h being the optimal time frame, and 48 h
being the end of the period during which drug administration can be
expected to reliably produce the desired outcome [258].
A very serious possible complication is Reye’s syndrome, a pathology
with diverse symptomatology which occurs in children that are infected
with a virus, the causes of which are not yet clear, but it is thought
to be caused by consuming acetylsalicylic acid in the context of the
viral infection [264].
A
case study showed that capsaicin may be used effectively to affect the
viral neuraminidase, which is integral in the cellular invasion process [254].
Interestingly, a type of capsaicin-sensitive neurons of the respiratory
tract may be instrumental in combating influenza infections, after they
have been activated by capsaicin [265], but this is still the subject of further research.
5.2. Antiviral Activity against the Lassa Virus
Lassa virus (LASV) is an endemic pathogen in West Africa responsible for causing a haemorrhagic fever by the same name [266]. The reservoir of the virus are the rodents Mastomys nataliensis [267,268]. The pathogen has been recently recorded outside of its endemic radius [268],
a reason for concern among the healthcare professionals. The World
Health Organization (WHO) has incentivized the development of a vaccine
against Lassa [268], which should come as no surprise given its high morbidity and mortality [268] as well as the limited therapeutic options currently available [255].
Capsaicin
has been found to be able to inhibit the entry of Lassa virus into
permissible cells by blocking the LASV-GP mediated fusion and by binding
directly to the LASV pseudovirions [255].
The inhibition of entry is made possible due to the fact that capsaicin
affects the stable signal peptide-GP2 transmembrane region of the
virus’ glycoprotein [255].
Despite Lassa’s great genetic diversity, capsaicin proved to be
effective in comparable rates against multiple different strains [255].
6. Discussion
The
rapid development of phytochemistry during the last decades offers new
possibilities and opportunities in the fight against numerous different
pathogens. The approaches of phytomedicine are based both in traditional
medicine practises—there is extensive research on ethnobotany (e.g., [269,270,271,272,273,274])—and modern biochemical research. Capsaicin is just one of the numerous phytochemicals, such as kaempferol (e.g., [6,13,14]), quercetin [4,5,9], curcumin [275,276,277,278], coumarin (e.g., [3,7,279]) and allicin (e.g., [8,12,280]), which have been under research for quite some time for their antimicrobial properties.
As
presented in the paper, there is much evidence to suggest that a host
of mechanisms exists offering promise that capsaicin, alone or in
combination with other compounds, can be, albeit sometimes in high
concentrations, effective in an antimicrobial role. As mentioned, most
of the pathogens against which capsaicin has been tested, are not only
dangerous, especially in immunocompromised hosts or in nosocomial
settings, but exhibit an even increasing resistance to existing
therapies.
It must be noted that capsaicin has a variety of proven health-related properties, namely analgesic, [281,282], antioxidant [283], anti-inflammatory [284,285], anti-cancer [286,287,288,289,290,291,292], cardio-protective [293], vasculomodulatory [294], and metabolic modulation [283,295,296] effects; more organ-specific effects have been also mentioned [297].
Apart from these actions, an extensive number of traditional
applications of capsaicin have been reported from Central and South
America [298,299] where the red chili peppers where first cultivated, and even India [300] and Eritrea [301].
Of particular note, the native chilli of India, ‘Bhoot Jolokia’
(Capsicum chinense Jacq.), is regarded as the hottest chilli in the
world, and has a host of applications in Ayurveda, the traditional
Indian medicine [302].
On
another aspect, repeated administration of capsaicin was proved by
numerous researchers to inhibit the production and/or action of
substance P [38,282,303,304,305,306,307,308,309] at least when locally applied. This is important, because apart from the other actions of substance P [310,311,312,313], it is implicated in the negative effects of infection-associated inflammation in animal models [314,315] and in teeth [316];
a recent review, also examined the association between the defensive
capacity of the respiratory system and substance P in the context of the
COVID-19 infection [317].
Therefore, in theory, for a patient suffering from a pathogen
susceptible to capsaicin, the compound could exert a dual action, both a
direct inhibition of the pathogen and a lessening of the associated
inflammation.
We would also like to note that capsaicin-sensitive neurons can release somatostatin [285,318] and it is already well known that somatostatin promotes anti-inflammatory and anti-nociceptive effects [319,320,321];
recently, capsaicin was shown to be able to induce the release of
somatostatin from such nerve endings when applied in transdermal patches
[322].
Somatostatin is also important in its immunomodulatory role in cases of
infection-induced inflammation; despite some positive effects, the
secretion of somatostatin seems to downregulate the immune system [323,324,325,326].
Therefore, we could hypothesise that a capsaicin-derived antimicrobial
drug could, at least in sufficient concentration, both act directly
against the pathogen itself and also modulate the immune response by
promoting somatostatin activity. However, another aspect we should
consider here is that somatostatin and its analogues are evaluated as
anticancer agents [327,328,329,330,331,332] and this can have implications in the case of viral-induced cancers [333,334,335,336].
Another
important aspect related to the antimicrobial properties of capsaicin
are its applications in neuropathy. Peripheral neuropathy may arise due
to various causes such as type 2 diabetes, metabolic disorders or due to
a considerable number of infectious agents as discussed by Brizzi et
al. [337] and De León et al. [338]. On the other hand, a number of antimicrobial agents may also cause peripheral neuropathy themselves [338];
as such it is important to consider the potential applications as an
alternative in the treatment of infections where the antimicrobials have
this particular complication. Furthermore, capsaicin can be used to
treat neuropathic pain [339,340]
and therefore we may propose that capsaicin preparations can be used to
treat both infection-induced peripheral neuropathy and the original
infection itself. The effectiveness of such a treatment regarding the
neuropathy could be monitored by a number of blood tests as suggested by
a recent study [341]. Metabolic and systemic imbalances may aggravate the condition and should be taken into consideration [342,343].
Nonetheless,
some constraints must be mentioned at this point, regarding the
pharmacokinetics and pharmacotoxicity of capsaicin. As a compound, it is
liposoluble and can be consequently administered locally, orally, and
systemically [344]. The gastrointestinal absorption of capsaicin varies from 50% to 90% via a passive mechanism [345]; its rapid metabolization yields a number of active metabolites [346,347]. The half-life of capsaicin differs based on its application, from 25 min in systemic administration [348] to about 24 h in local administration [349,350].
It has been proven that it is possible to prolong capsaicin release and
thus effective half-life using a carbopol-based formulation [351]
specifically for antimicrobial applications. The metabolic pathways of
capsaicin, which are important from a pharmacological perspective have
been the subject of extensive research [352,353,354].
The development could lead to various applications, including
perioperative care of complicated surgical cases or long-term treatment
of infections in areas where antibiotic permeation is reduced [355,356,357,358].
While
capsaicin has current and potential clinical applications, its side
effects, which can be severe depending on the dose and application site
are not negligible; pulmonary [359,360], gastrointestinal [361,362], cardiovascular [363,364], and even CNS [365,366]
adverse effects have been reported. The adverse effect of capsaicin
when it comes into contact with the eyes are even more rapid and
pronounced [367].
This is of even greater importance in patients with impaired judgment
or vision deficit that may mistakenly apply or consume capsaicin outside
of the recommended use [368,369,370].
Another possibility is the use of composite creams containing
capsaicin, along with other materials like coconut oil, which preserve
medicinal capsaicin properties, while having a lower cost [371],
and perhaps less side effects; the beneficial synergistic effects of
coconut oil and capsaicin have also been noted by Trbojević Ivić et al. [372]. The antimicrobial effects of coconut oil have already been studied by a number of researchers (e.g., [373,374,375,376,377])
and it has been proposed that it can be a realistic antibacterial
solution, at least for local infections of mild-to-medium severity [378]; its combination with capsaicin may further enhance its potential.
The
aforementioned data raise some serious issues, namely as to how
capsaicin, in a medicinal formulation, can be used in an antimicrobial
role, reaching, in the affected tissues, concentrations sufficient
enough to be effective, but not as high as to cause unbearable or even
life-threatening side effects. This issue is further compounded by the
fact that capsaicin is toxic for children in lower doses compared to
adults [379];
this is even more problematic when considering that typically, most
pathogens are more dangerous for children than for immunocompetent
adults. Finally, in potential overdose cases, there is no way to speed
up the elimination of capsaicin. Rather, the only option is to treat the
intoxication symptoms until it is excreted [380].
A
possible answer to the limitations of systemic administration—local
administration with patches, creams, and other methods being an easier
matter—could be the use of nanoparticles to deliver capsaicin to its
target tissues, in sufficient quantities. Nanoparticles are already
considered as a potential effective carrier of antibiotics (e.g., [381,382,383]), while other nanoparticles themselves are being considered as theoretically useful antiviral agents [384,385,386]. The delivery of antifungal agents via nanoparticles is also possible [387,388,389], and lately nanoparticles are being considered in the research for antiparasitic drugs [390,391,392].
While most of this research deals with metal nanoparticles, lipid
nanoparticles are also a potential solution as discussed by Date et al. [393]. Another potential option for external applications could be the lipid nanoparticles used in wound care [394]. Successful applications of capsaicin-laden nanoparticles in vitro have also been included in our paper [171,205].
Overall,
capsaicin’s use as an antibacterial agent covers a wide spectrum of
pathogens; namely bacteria, both Gram positive and Gram negative,
belonging to Staphylococcus, Streptococcus, Bacillus, Listeria, Vibrio,
Acinetobacter, Helicobacter, Salmonella, Escherichia, Klebsiella,
Proteus, and Pseudomonas species, in addition to fungal species like
Candida and Aspergillus, as well as the parasites Toxopasma and
Trypanosoma and the Influenza and Lassa viruses. This is important
because most of the aforementioned microorganisms are commonly
encountered in clinical practice. Moreover, the rising resistance noted
in some strains alongside the side effects associated with the usual
antimicrobial agents highlights the need for auxiliary treatments.
7. Conclusions
We
conclude that capsaicin has a number of demonstrable antibacterial,
antifungal, antiparasitic, and antiviral actions, and at least in its
antibacterial role it is also considered as a promising perspective.
Although significant research has been performed on this subject, more
experiments are required in order to determine the effects of capsaicin
on a wider host of pathogens and to elucidate whether there are any
undiscovered mechanisms of action.
Experiments with the aim to
determine the capsaicin-induced inflammation in the cases of infections
with capsaicin-susceptible pathogens should also be performed, the end
goal being the designing of dual-purpose drugs; those having both an
antimicrobial and an anti-inflammatory potential. Indeed, in most of the
cases examined in this paper, the antimicrobial concentrations are
reasonably low, and even in cases when they are on the high end,
capsaicin may still be useful due to a lack of resistance, especially in
the case of bacteria.
An overview of the antimicrobial actions
of capsaicin may contribute to multiple fields, including chemistry,
medicine, homeopathy, traditional medicine, as well as other areas. This
may further serve as a starting point to additional research,
especially in this era marked by the increase in antimicrobial
resistance.
Future research perspectives on this
topic may include the closer examination of antimicrobial actions of
capsaicin reported by traditional medicine as well as the exploration of
more efficient nanoparticle carriers for antimicrobial capsaicin
formulations. However, in any case, the most important research effort
should be directed towards the applications of capsaicin against
pathogens which are resistant to currently available medications.
Funding Statement
This
work was partially supported by a grant of the Ministry of Research,
Innovation and Digitization, CCCDI—UEFISCDI, project number
PN-III-P2-2.1-PED-2021-2243, within PNCDI III.
Author Contributions
Conceptualization,
A.-T.P., A.P., C.S. and C.C.; resources, K.P., A.C., I.A.B. and
I.S.-F.; writing—original draft preparation, A.-T.P., A.P., K.P., A.C.,
I.A.B., I.S.-F., C.S. and C.C.; writing—review and editing, A.-T.P.,
A.P., C.S. and C.C.; supervision, C.S. and C.C. All authors have read
and agreed to the published version of the manuscript.
Institutional Review Board Statement
Not applicable.
Informed Consent Statement
Not applicable.
Data Availability Statement
Not applicable.
Conflicts of Interest
The
authors declare no conflict of interest. The sponsors had no role in
the design, execution, interpretation, or writing of the study.
Footnotes
Disclaimer/Publisher’s Note:
The statements, opinions and data contained in all publications are
solely those of the individual author(s) and contributor(s) and not of
MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim
responsibility for any injury to people or property resulting from any
ideas, methods, instructions or products referred to in the content.
References
2.
Brinkac L., Voorhies A., Gomez A., Nelson K.E. The Threat of Antimicrobial Resistance on the Human Microbiome. Microb. Ecol. 2017;74:1001–1008. doi: 10.1007/s00248-017-0985-z. [PMC free article] [PubMed] [CrossRef] [Google Scholar]3.
Ojala
T., Remes S., Haansuu P., Vuorela H., Hiltunen R., Haahtela K., Vuorela
P. Antimicrobial activity of some coumarin containing herbal plants
growing in Finland. J. Ethnopharmacol. 2000;73:299–305. doi: 10.1016/S0378-8741(00)00279-8. [PubMed] [CrossRef] [Google Scholar]4.
Hirai I., Okuno M., Katsuma R., Arita N., Tachibana M., Yamamoto Y. Characterisation of anti-Staphylococcus aureus activity of quercetin. Int. J. Food Sci. Technol. 2010;45:1250–1254. doi: 10.1111/j.1365-2621.2010.02267.x. [CrossRef] [Google Scholar]5.
Shu Y., Liu Y., Li L., Feng J., Lou B., Zhou X., Wu H. Antibacterial activity of quercetin on oral infectious pathogens. Afr. J. Microbiol. Res. 2011;5:5358–5361. [Google Scholar]6.
Tatsimo
S.J.N., Tamokou J.d.D., Havyarimana L., Csupor D., Forgo P., Hohmann
J., Kuiate J.-R., Tane P. Antimicrobial and antioxidant activity of
kaempferol rhamnoside derivatives from Bryophyllum pinnatum. BMC Res. Notes. 2012;5:158. doi: 10.1186/1756-0500-5-158. [PMC free article] [PubMed] [CrossRef] [Google Scholar]7.
Al-
Rifai A.A.A., Ayoub M.T., Shakya A.K., Abu Safieh K.A., Mubarak M.S.
Synthesis, characterization, and antimicrobial activity of some new
coumarin derivatives. Med. Chem. Res. 2012;21:468–476. doi: 10.1007/s00044-011-9553-0. [CrossRef] [Google Scholar]8.
Wallock-
Richards D., Doherty C.J., Doherty L., Clarke D.J., Place M., Govan
J.R.W., Campopiano D.J. Garlic Revisited: Antimicrobial Activity of
Allicin-Containing Garlic Extracts against Burkholderia cepacia Complex. PLoS ONE. 2014;9:e112726. doi: 10.1371/journal.pone.0112726. [PMC free article] [PubMed] [CrossRef] [Google Scholar]9.
Jaisinghani R.N. Antibacterial properties of quercetin. Microbiol. Res. 2017;8:6877. doi: 10.4081/mr.2017.6877. [CrossRef] [Google Scholar]10.
Di
Sotto A., Di Giacomo S., Amatore D., Locatelli M., Vitalone A., Toniolo
C., Rotino G., Lo Scalzo R., Palamara A., Marcocci M.E., et al. A
Polyphenol Rich Extract from Solanum melongena L. DR2 Peel Exhibits Antioxidant Properties and Anti-Herpes Simplex Virus Type 1 Activity In Vitro. Molecules. 2018;23:2066. doi: 10.3390/molecules23082066. [PMC free article] [PubMed] [CrossRef] [Google Scholar]11.
Di
Sotto A., Checconi P., Celestino I., Locatelli M., Carissimi S., De
Angelis M., Rossi V., Limongi D., Toniolo C., Martinoli L., et al.
Antiviral and Antioxidant Activity of a Hydroalcoholic Extract from Humulus lupulus L. Oxidative Med. Cell. Longev. 2018;2018:5919237. doi: 10.1155/2018/5919237. [PMC free article] [PubMed] [CrossRef] [Google Scholar]12.
Nakamoto
M., Kunimura K., Suzuki J.I., Kodera Y. Antimicrobial properties of
hydrophobic compounds in garlic: Allicin, vinyldithiin, ajoene and
diallyl polysulfides (Review) Exp. Ther. Med. 2020;19:1550–1553. doi: 10.3892/etm.2019.8388. [PMC free article] [PubMed] [CrossRef] [Google Scholar]13.
Periferakis
A., Periferakis K., Badarau I.A., Petran E.M., Popa D.C., Caruntu A.,
Costache R.S., Scheau C., Caruntu C., Costache D.O. Kaempferol:
Antimicrobial Properties, Sources, Clinical, and Traditional
Applications. Int. J. Mol. Sci. 2022;23:15054. doi: 10.3390/ijms232315054. [PMC free article] [PubMed] [CrossRef] [Google Scholar]14.
Bangar
S.P., Chaudhary V., Sharma N., Bansal V., Ozogul F., Lorenzo J.M.
Kaempferol: A flavonoid with wider biological activities and its
applications. Crit. Rev. Food Sci. Nutr. 2022:1–25. doi: 10.1080/10408398.2022.2067121. [PubMed] [CrossRef] [Google Scholar]15.
Vuković S., Popović-Djordjević J.B., Kostić A.Ž., Pantelić N.D., Srećković N., Akram M., Laila U., Katanić Stanković J.S. Allium Species in the Balkan Region–Major Metabolites, Antioxidant and Antimicrobial Properties. Horticulturae. 2023;9:408. doi: 10.3390/horticulturae9030408. [CrossRef] [Google Scholar]16.
Valipour
M., Hosseini A., Di Sotto A., Irannejad H. Dual action
anti-inflammatory/antiviral isoquinoline alkaloids as potent naturally
occurring anti-SARS-CoV-2 agents: A combined pharmacological and
medicinal chemistry perspective. Phytother. Res. 2023;37:2168–2186. doi: 10.1002/ptr.7833. [PubMed] [CrossRef] [Google Scholar]17.
Cordell G.A., Araujo O.E. Capsaicin: Identification, nomenclature, and pharmacotherapy. Ann. Pharmacother. 1993;27:330–336. doi: 10.1177/106002809302700316. [PubMed] [CrossRef] [Google Scholar]18.
Srinivasan K. Biological Activities of Red Pepper (Capsicum annuum) and Its Pungent Principle Capsaicin: A Review. Crit. Rev. Food Sci. Nutr. 2016;56:1488–1500. doi: 10.1080/10408398.2013.772090. [PubMed] [CrossRef] [Google Scholar]19.
Naves E.R., de Ávila Silva L., Sulpice R., Araújo W.L., Nunes-Nesi A., Peres L.E.P., Zsögön A. Capsaicinoids: Pungency beyond Capsicum. Trends Plant Sci. 2019;24:109–120. doi: 10.1016/j.tplants.2018.11.001. [PubMed] [CrossRef] [Google Scholar]20.
Gradinaru T.C., Petran M., Dragos D., Gilca M. PlantMolecularTasteDB: A Database of Taste Active Phytochemicals. Front. Pharmacol. 2021;12:751712. doi: 10.3389/fphar.2021.751712. [PMC free article] [PubMed] [CrossRef] [Google Scholar]21.
Alberti
A., Galasso V., Kovac B., Modelli A., Pichierri F. Probing the
molecular and electronic structure of capsaicin: A spectroscopic and
quantum mechanical study. J. Phys. Chem. A. 2008;112:5700–5711. doi: 10.1021/jp801890g. [PubMed] [CrossRef] [Google Scholar]22.
Reyes-Escogido Mde L., Gonzalez-Mondragon E.G., Vazquez-Tzompantzi E. Chemical and pharmacological aspects of capsaicin. Molecules. 2011;16:1253–1270. doi: 10.3390/molecules16021253. [PMC free article] [PubMed] [CrossRef] [Google Scholar]23.
Bennett D.J., Kirby G.W. Constitution and biosynthesis of capsaicin. J. Chem. Soc. C Org. 1968:442–446. doi: 10.1039/j39680000442. [CrossRef] [Google Scholar]24.
Leete E., Louden M.C.L. Biosynthesis of capsaicin and dihydrocapsaicin in Capsicum frutescens. J. Am. Chem. Soc. 1968;90:6837–6841. doi: 10.1021/ja01026a049. [PubMed] [CrossRef] [Google Scholar]25.
Aza-González C., Núñez-Palenius H.G., Ochoa-Alejo N. Molecular biology of capsaicinoid biosynthesis in chili pepper (Capsicum spp.) Plant Cell Rep. 2011;30:695–706. doi: 10.1007/s00299-010-0968-8. [PubMed] [CrossRef] [Google Scholar]26.
Kaiser M., Higuera I., Goycoolea F.M. Fruit and Vegetable Phytochemicals. Wiley; Hoboken, NJ, USA: 2017. Capsaicinoids: Occurrence, Chemistry, Biosynthesis, and Biological Effects; pp. 499–514. [CrossRef] [Google Scholar]27.
Katsuragi
H., Shimoda K., Yamamoto R., Ohara T., Hamada H. Enzymatic synthesis of
capsaicin 4-O-β-xylooligosaccharides by β-xylosidase from Aspergillus sp. Acta. Biol. Hung. 2011;62:151–155. doi: 10.1556/ABiol.62.2011.2.5. [PubMed] [CrossRef] [Google Scholar]28.
Cowles
R.S., Keller J.E., Miller J.R. Pungent spices, ground red pepper, and
synthetic capsaicin as onion fly ovipositional deterrents. J. Chem. Ecol. 1989;15:719–730. doi: 10.1007/BF01014714. [PubMed] [CrossRef] [Google Scholar]29.
Kimball B.A., Taylor J., Perry K.R., Capelli C. Deer responses to repellent stimuli. J. Chem. Ecol. 2009;35:1461–1470. doi: 10.1007/s10886-009-9721-6. [PubMed] [CrossRef] [Google Scholar]31.
Yang
N., Galves C., Racioni Goncalves A.C., Chen J., Fisk I. Impact of
capsaicin on aroma release: In vitro and in vivo analysis. Food Res. Int. 2020;133:109197. doi: 10.1016/j.foodres.2020.109197. [PMC free article] [PubMed] [CrossRef] [Google Scholar]32.
Hu
X., Ayed C., Chen J., Fisk I., Yang N. The role of capsaicin
stimulation on the physicochemical properties of saliva and aroma
release in model aqueous and oil systems. Food Chem. 2022;386:132824. doi: 10.1016/j.foodchem.2022.132824. [PubMed] [CrossRef] [Google Scholar]33.
Maliszewska
J., Wyszkowska J., Kletkiewicz H., Rogalska J. Capsaicin-induced
dysregulation of acid-base status in the American cockroach. J. Environ. Sci. Health B. 2019;54:676–680. doi: 10.1080/03601234.2019.1632642. [PubMed] [CrossRef] [Google Scholar]34.
Cui
S.-F., Wang J.-W., Li H.-F., Fang R., Yu X., Lu Y.-J.
Microencapsulation of Capsaicin in Chitosan Microcapsules:
Characterization, Release Behavior, and Pesticidal Properties against Tribolium castaneum (Herbst) Insects. 2023;14:27. doi: 10.3390/insects14010027. [PMC free article] [PubMed] [CrossRef] [Google Scholar]35.
Adaszek
Ł., Gadomska D., Mazurek Ł., Łyp P., Madany J., Winiarczyk S.
Properties of capsaicin and its utility in veterinary and human
medicine. Res. Vet. Sci. 2019;123:14–19. doi: 10.1016/j.rvsc.2018.12.002. [PubMed] [CrossRef] [Google Scholar]36.
Mohammad
S., Mustofa Helmi E., Faisal F., Muhammad Thohawi Elziyad P. Role of
Capsaicin in the Repair of Cellular Activity in Mice Liver. Pharmacogn. J. 2021;13:1573–1576. [Google Scholar]37.
Watson P.N.C., Evans R.J. The postmastectomy pain syndrome and topical capsaicin: A randomized trial. Pain. 1992;51:375–379. doi: 10.1016/0304-3959(92)90223-X. [PubMed] [CrossRef] [Google Scholar]38.
McCleane
G. The analgesic efficacy of topical capsaicin is enhanced by glyceryl
trinitrate in painful osteoarthritis: A randomized, double blind,
placebo controlled study. Eur. J. Pain. 2000;4:355–360. doi: 10.1053/eujp.2000.0200. [PubMed] [CrossRef] [Google Scholar]39.
Grushka M., Epstein J.B., Gorsky M. Burning mouth syndrome. Am. Fam. Physician. 2002;65:615–620. [PubMed] [Google Scholar]40.
Saguil A., Kane S., Mercado M., Lauters R. Herpes Zoster and Postherpetic Neuralgia: Prevention and Management. Am. Fam. Physician. 2017;96:656–663. [PubMed] [Google Scholar]41.
Breneman
D.L., Cardone J.S., Blumsack R.F., Lather R.M., Searle E.A., Pollack
V.E. Topical capsaicin for treatment of hemodialysis-related pruritus. J. Am. Acad. Dermatol. 1992;26:91–94. doi: 10.1016/0190-9622(92)70013-6. [PubMed] [CrossRef] [Google Scholar]42.
Lysy
J., Sistiery-Ittah M., Israelit Y., Shmueli A., Strauss-Liviatan N.,
Mindrul V., Keret D., Goldin E. Topical capsaicin—A novel and effective
treatment for idiopathic intractable pruritus ani: A randomised, placebo
controlled, crossover study. Gut. 2003;52:1323–1326. doi: 10.1136/gut.52.9.1323. [PMC free article] [PubMed] [CrossRef] [Google Scholar]43.
Makhlough
A., Ala S., Haj-Heydari Z., Kashi Z., Bari A. Topical capsaicin therapy
for uremic pruritus in patients on hemodialysis. Iran J. Kidney Dis. 2010;4:137–140. [PubMed] [Google Scholar]44.
Gooding S.M., Canter P.H., Coelho H.F., Boddy K., Ernst E. Systematic review of topical capsaicin in the treatment of pruritus. Int. J. Dermatol. 2010;49:858–865. doi: 10.1111/j.1365-4632.2010.04537.x. [PubMed] [CrossRef] [Google Scholar]45.
de
Sèze M., Wiart L., de Sèze M.P., Soyeur L., Dosque J.P., Blajezewski
S., Moore N., Brochet B., Mazaux J.M., Barat M., et al. Intravesical
capsaicin versus resiniferatoxin for the treatment of detrusor
hyperreflexia in spinal cord injured patients: A double-blind,
randomized, controlled study. J. Urol. 2004;171:251–255. doi: 10.1097/01.ju.0000100385.93801.d4. [PubMed] [CrossRef] [Google Scholar]46.
Cruz F. Mechanisms involved in new therapies for overactive bladder. Urology. 2004;63:65–73. doi: 10.1016/j.urology.2003.11.001. [PubMed] [CrossRef] [Google Scholar]47.
Misra M.N., Pullani A.J., Mohamed Z.U. Prevention of PONV by acustimulation with Capsicum plaster is comparable to ondansetron after middle ear surgery. Can. J. Anaesth. 2005;52:485–489. doi: 10.1007/BF03016527. [PubMed] [CrossRef] [Google Scholar]48.
Agarwal
A., Dhiraaj S., Tandon M., Singh P.K., Singh U., Pawar S. Evaluation of
capsaicin ointment at the Korean hand acupressure point K-D2 for
prevention of postoperative nausea and vomiting. Anaesthesia. 2005;60:1185–1188. doi: 10.1111/j.1365-2044.2005.04402.x. [PubMed] [CrossRef] [Google Scholar]49.
Hayman M., Kam P.C.A. Capsaicin: A review of its pharmacology and clinical applications. Curr. Anaesth. Crit. Care. 2008;19:338–343. doi: 10.1016/j.cacc.2008.07.003. [CrossRef] [Google Scholar]50.
Botonis
P.G., Miliotis P.G., Kounalakis S.N., Koskolou M.D., Geladas N.D.
Effects of capsaicin application on the skin during resting exposure to
temperate and warm conditions. Scand J. Med. Sci. Sports. 2019;29:171–179. doi: 10.1111/sms.13317. [PubMed] [CrossRef] [Google Scholar]51.
Rothenberger
J., Wittwer M., Tschumi C., Constantinescu M.A., Daigeler A., Olariu R.
Quantitative impact analysis of remote ischemic conditioning and
capsaicin application on human skin microcirculation. Clin. Hemorheol. Microcirc. 2019;71:291–298. doi: 10.3233/CH-180373. [PubMed] [CrossRef] [Google Scholar]52.
Caruntu
C., Negrei C., Ilie Ghita M., Caruntu A., Bădărău A.I., Ioan B., Boda
D., Albu A., Brănişteanu D. Capsaicin, a Hot Topic in Skin Pharmacology
and Physiology. Inflammation. 2015;63:487–491. [Google Scholar]53.
Ilie
Ghita M., Caruntu C., Tampa M., Georgescu S.R., Matei C., Negrei C.,
Ion R.-M., Constantin C., Neagu M., Boda D. Capsaicin: Physicochemical
properties, cutaneous reactions and potential applications in painful
and inflammatory conditions (Review) Exp. Ther. Med. 2019;18:916–925. [PMC free article] [PubMed] [Google Scholar]54.
Căruntu
C., Boda D. Evaluation through in vivo reflectance confocal microscopy
of the cutaneous neurogenic inflammatory reaction induced by capsaicin
in human subjects. J. Biomed. Opt. 2012;17:085003. doi: 10.1117/1.JBO.17.8.085003. [PubMed] [CrossRef] [Google Scholar]55.
Lakatos
S., Jancsó G., Horváth Á., Dobos I., Sántha P. Longitudinal Study of
Functional Reinnervation of the Denervated Skin by Collateral Sprouting
of Peptidergic Nociceptive Nerves Utilizing Laser Doppler Imaging. Front. Physiol. 2020;11:439. doi: 10.3389/fphys.2020.00439. [PMC free article] [PubMed] [CrossRef] [Google Scholar]56.
Wallace R.J. Antimicrobial properties of plant secondary metabolites. Proc. Nutr. Soc. 2004;63:621–629. doi: 10.1079/PNS2004393. [PubMed] [CrossRef] [Google Scholar]57.
Salehi
B., Zakaria Z.A., Gyawali R., Ibrahim S.A., Rajkovic J., Shinwari Z.K.,
Khan T., Sharifi-Rad J., Ozleyen A., Turkdonmez E., et al. Piper
Species: A Comprehensive Review on Their Phytochemistry, Biological
Activities and Applications. Molecules. 2019;24:1364. doi: 10.3390/molecules24071364. [PMC free article] [PubMed] [CrossRef] [Google Scholar]58.
Makuwa
S.C., Serepa-Dlamini M.H. The Antibacterial Activity of Crude Extracts
of Secondary Metabolites from Bacterial Endophytes Associated with Dicoma anomala. Int. J. Microbiol. 2021;2021:8812043. doi: 10.1155/2021/8812043. [PMC free article] [PubMed] [CrossRef] [Google Scholar]59.
Aminah
N.S., Laili E.R., Rafi M., Rochman A., Insanu M., Tun K.N.W. Secondary
metabolite compounds from Sida genus and their bioactivity. Heliyon. 2021;7:e06682. doi: 10.1016/j.heliyon.2021.e06682. [PMC free article] [PubMed] [CrossRef] [Google Scholar]60.
Jubair
N., Rajagopal M., Chinnappan S., Abdullah N.B., Fatima A. Review on the
Antibacterial Mechanism of Plant-Derived Compounds against
Multidrug-Resistant Bacteria (MDR) Evid. Based Complement Altern. Med. 2021;2021:3663315. doi: 10.1155/2021/3663315. [PMC free article] [PubMed] [CrossRef] [Google Scholar]61.
Bhatia
P., Sharma A., George A.J., Anvitha D., Kumar P., Dwivedi V.P., Chandra
N.S. Antibacterial activity of medicinal plants against ESKAPE: An
update. Heliyon. 2021;7:e06310. doi: 10.1016/j.heliyon.2021.e06310. [PMC free article] [PubMed] [CrossRef] [Google Scholar]62.
Füchtbauer
S., Mousavi S., Bereswill S., Heimesaat M.M. Antibacterial properties
of capsaicin and its derivatives and their potential to fight antibiotic
resistance—A literature survey. Eur. J. Microbiol. Immunol. 2021;11:10–17. doi: 10.1556/1886.2021.00003. [PMC free article] [PubMed] [CrossRef] [Google Scholar]63.
Kitsos N., Cassimos D., Xinias I., Agakidis C., Mavroudi A. Management of antibiotic allergy in children: A practical approach. Allergol. Immunopathol. 2022;50:30–38. doi: 10.15586/aei.v50i5.607. [PubMed] [CrossRef] [Google Scholar]64.
Green E.A., Fogarty K., Ishmael F.T. Penicillin Allergy: Mechanisms, Diagnosis, and Management. Prim. Care. 2023;50:221–235. doi: 10.1016/j.pop.2022.11.002. [PubMed] [CrossRef] [Google Scholar]65.
Wrynn A.F. An overview of penicillin allergies for nurses. Nursing. 2023;53:27–31. doi: 10.1097/01.NURSE.0000923664.66265.a4. [PubMed] [CrossRef] [Google Scholar]66.
Westphal J., Vetter D., Brogard J. Hepatic side-effects of antibiotics. J. Antimicrob. Chemother. 1994;33:387–401. doi: 10.1093/jac/33.3.387. [PubMed] [CrossRef] [Google Scholar]67.
Thiim M., Friedman L.S. Hepatotoxicity of antibiotics and antifungals. Clin. Liver Dis. 2003;7:381–399. doi: 10.1016/S1089-3261(03)00021-7. [PubMed] [CrossRef] [Google Scholar]68.
Polson J.E. Hepatotoxicity due to antibiotics. Clin. Liver Dis. 2007;11:549–561. doi: 10.1016/j.cld.2007.06.009. [PubMed] [CrossRef] [Google Scholar]70.
Rehman K., Kamran S.H., Hamid Akash M.S. Chapter 16—Toxicity of antibiotics. In: Hashmi M.Z., editor. Antibiotics and Antimicrobial Resistance Genes in the Environment. Volume 1. Elsevier; Amsterdam, The Netherlands: 2020. pp. 234–252. [Google Scholar]71.
Dorobăţ O.-M., Moisoiu A., Tălăpan D. Bacteria isolated from pleural fluid and their resistance to antimicrobials. Pneumologia. 2006;55:47–51. [PubMed] [Google Scholar]72.
Dorobăţ
O.M., Moisoiu A., Tălăpan D. Incidence and resistance patterns of
pathogens from lower respiratory tract infections (LRTI) Pneumologia. 2007;56:7–15. [PubMed] [Google Scholar]73.
Dorobăţ O.M., Bădicuţ I., Tălăpan D., Tenea C., Rafila A. Antibiotic resistance of Gram-positive cocci isolated in 2008. Bacteriol. Virusol. Parazitol. Epidemiol. 2010;55:83–92. [PubMed] [Google Scholar]74.
Popescu
G.A., Șerban R., Iosif I., Codiță I., Dorobăț O., Tălăpan D., Buzea M.,
Szekely E., Dorneanu O., Bota K., et al. Antimicrobial resistance of
germs isolated from invasive infections–Romania 2012. BMC Infect. Dis. 2013;13:O16. doi: 10.1186/1471-2334-13-S1-O16. [CrossRef] [Google Scholar]75.
Rafila
A., Talapan D., Dorobăţ O.M., Popescu G.A., Piţigoi D., Florea D.,
Buicu F.C. Emergence of Carbapenemase-producing Enterobacteriaceae, a
Public Health Threat: A Romanian Infectious Disease Hospital Based
Study/Emergenţa Enterobacteriaceaelor producătoare de carbapenemaze, o
ameninţare pentru sănătatea publică: Un studiu realizat într-un spital
romanesc de boli infectioase. Rev. Romana Med. Lab. 2015;23:295–301. doi: 10.1515/rrlm-2015-0024. [CrossRef] [Google Scholar]76.
Kohler
P.P., Melano R.G., Patel S.N., Shafinaz S., Faheem A., Coleman B.L.,
Green K., Armstrong I., Almohri H., Borgia S., et al. Emergence of
Carbapenemase-Producing Enterobacteriaceae, South-Central Ontario,
Canada. Emerg. Infect. Dis. 2018;24:1674–1682. doi: 10.3201/eid2409.180164. [PMC free article] [PubMed] [CrossRef] [Google Scholar]77.
Tălăpan
D., Rafila A. Five-Year Survey of Asymptomatic Colonization with
Multidrug-Resistant Organisms in a Romanian Tertiary Care Hospital. Infect. Drug Resist. 2022;15:2959–2967. doi: 10.2147/IDR.S360048. [PMC free article] [PubMed] [CrossRef] [Google Scholar]78.
Ackerman S., Gonzales R. The context of antibiotic overuse. Ann. Intern. Med. 2012;157:211–212. doi: 10.7326/0003-4819-157-3-201208070-00013. [PubMed] [CrossRef] [Google Scholar]80.
Willis
L.D., Chandler C. Quick fix for care, productivity, hygiene and
inequality: Reframing the entrenched problem of antibiotic overuse. BMJ Glob. Health. 2019;4:e001590. doi: 10.1136/bmjgh-2019-001590. [PMC free article] [PubMed] [CrossRef] [Google Scholar]81.
Kanellopoulos
C., Lamprinou V., Politi A., Voudouris P., Iliopoulos I., Kokkaliari
M., Moforis L., Economou-Amilli A. Microbial Mat Stratification in
Travertine Depositions of Greek Hot Springs and Biomineralization
Processes. Minerals. 2022;12:1408. doi: 10.3390/min12111408. [CrossRef] [Google Scholar]82.
Kanellopoulos
C., Lamprinou V., Politi A., Voudouris P., Iliopoulos I., Kokkaliari
M., Moforis L., Economou-Amilli A. Speleothems and Biomineralization
Processes in Hot Spring Environment: The Case of Aedipsos (Edipsos),
Euboea (Evia) Island, Greece. J. Mar. Sci. Eng. 2022;10:1909. doi: 10.3390/jmse10121909. [CrossRef] [Google Scholar]83.
Kanellopoulos
C., Lamprinou V., Politi A., Voudouris P., Economou-Amilli A. Pioneer
species of Cyanobacteria in hot springs and their role to travertine
formation: The case of Aedipsos hot springs, Euboea (Evia), Greece. Depos. Rec. 2022;8:1079–1092. doi: 10.1002/dep2.198. [CrossRef] [Google Scholar]84.
EUCAST Definitive Document Methods for the determination of susceptibility of bacteria to antimicrobial agents. Terminology. Clin Microbiol Infect. 1998;4:291. [PubMed] [Google Scholar]85.
Nascimento
P.L., Nascimento T.C., Ramos N.S., Silva G.R., Gomes J.E., Falcão R.E.,
Moreira K.A., Porto A.L., Silva T.M. Quantification, antioxidant and
antimicrobial activity of phenolics isolated from different extracts of Capsicum frutescens (Pimenta Malagueta) Molecules. 2014;19:5434–5447. doi: 10.3390/molecules19045434. [PMC free article] [PubMed] [CrossRef] [Google Scholar]86.
Das J., Deka M., Gogoi K. Antimicrobial activity of chilli extracts (Capsicum chinense) against food borne pathogens Escherichia coli and Staphylococcus aureus. Int. J. Res. Anal. Rev. 2018;5:717–720. [Google Scholar]87.
Marini
E., Magi G., Mingoia M., Pugnaloni A., Facinelli B. Antimicrobial and
Anti-Virulence Activity of Capsaicin against Erythromycin-Resistant,
Cell-Invasive Group A Streptococci. Front. Microbiol. 2015;6:1281. doi: 10.3389/fmicb.2015.01281. [PMC free article] [PubMed] [CrossRef] [Google Scholar]88.
Omolo
M.A., Wong Z.-Z., Borh W.G., Hedblom G.A., Dev K., Baumler D.J.
Comparative analysis of capsaicin in twenty nine varieties of unexplored
Capsicum and its antimicrobial activity against bacterial and fungal pathogens. J. Med. Plants Res. 2018;12:544–556. [Google Scholar]89.
Chatterjee
S., Asakura M., Chowdhury N., Neogi S.B., Sugimoto N., Haldar S.,
Awasthi S.P., Hinenoya A., Aoki S., Yamasaki S. Capsaicin, a potential
inhibitor of cholera toxin production in Vibrio cholerae. FEMS Microbiol. Lett. 2010;306:54–60. doi: 10.1111/j.1574-6968.2010.01931.x. [PubMed] [CrossRef] [Google Scholar]90.
Ozçelik
B., Kartal M., Orhan I. Cytotoxicity, antiviral and antimicrobial
activities of alkaloids, flavonoids, and phenolic acids. Pharm. Biol. 2011;49:396–402. doi: 10.3109/13880209.2010.519390. [PubMed] [CrossRef] [Google Scholar]91.
Zeyrek F.Y., Oguz E. In vitro activity of capsaicin against Helicobacter pylori. Ann. Microbiol. 2005;55:125–127. [Google Scholar]92.
Ayariga J.A., Abugri D.A., Amrutha B., Villafane R. Capsaicin Potently Blocks Salmonella typhimurium Invasion of Vero Cells. Antibiotics. 2022;11:666. doi: 10.3390/antibiotics11050666. [PMC free article] [PubMed] [CrossRef] [Google Scholar]93.
Kushwaha
M., Jain S.K., Sharma N., Abrol V., Jaglan S., Vishwakarma R.A.
Establishment of LCMS Based Platform for Discovery of Quorum Sensing
Inhibitors: Signal Detection in Pseudomonas aeruginosa PAO1. ACS Chem. Biol. 2018;13:657–665. doi: 10.1021/acschembio.7b00875. [PubMed] [CrossRef] [Google Scholar]94.
Ahmad-Mansour N., Loubet P., Pouget C., Dunyach-Remy C., Sotto A., Lavigne J.P., Molle V. Staphylococcus aureus Toxins: An Update on Their Pathogenic Properties and Potential Treatments. Toxins. 2021;13:677. doi: 10.3390/toxins13100677. [PMC free article] [PubMed] [CrossRef] [Google Scholar]95.
Leung A.K.C., Barankin B., Leong K.F. Staphylococcal-scalded skin syndrome: Evaluation, diagnosis, and management. World J. Pediatr. 2018;14:116–120. doi: 10.1007/s12519-018-0150-x. [PubMed] [CrossRef] [Google Scholar]96.
Lowy F.D. Staphylococcus aureus infections. N. Engl. J. Med. 1998;339:520–532. doi: 10.1056/NEJM199808203390806. [PubMed] [CrossRef] [Google Scholar]97.
Tong S.Y., Davis J.S., Eichenberger E., Holland T.L., Fowler V.G., Jr. Staphylococcus aureus infections: Epidemiology, pathophysiology, clinical manifestations, and management. Clin. Microbiol. Rev. 2015;28:603–661. doi: 10.1128/CMR.00134-14. [PMC free article] [PubMed] [CrossRef] [Google Scholar]98.
Stevens D.L. The toxins of group A streptococcus, the flesh eating bacteria. Immunol. Investig. 1997;26:129–150. doi: 10.3109/08820139709048921. [PubMed] [CrossRef] [Google Scholar]100.
Howden B.P., Davies J.K., Johnson P.D., Stinear T.P., Grayson M.L. Reduced vancomycin susceptibility in Staphylococcus aureus,
including vancomycin-intermediate and heterogeneous
vancomycin-intermediate strains: Resistance mechanisms, laboratory
detection, and clinical implications. Clin. Microbiol. Rev. 2010;23:99–139. doi: 10.1128/CMR.00042-09. [PMC free article] [PubMed] [CrossRef] [Google Scholar]101.
Grema H.A., Geidam Y.A., Gadzama G.B., Ameh J.A., Suleiman A. Methicillin resistant Staphylococcus aureus (MRSA): A review. Adv. Anim. Vet. Sci. 2015;3:79–98. doi: 10.14737/journal.aavs/2015/3.2.79.98. [CrossRef] [Google Scholar]102.
Akyuz
L., Kaya M., Mujtaba M., Ilk S., Sargin I., Salaberria A.M., Labidi J.,
Cakmak Y.S., Islek C. Supplementing capsaicin with chitosan-based films
enhanced the anti-quorum sensing, antimicrobial, antioxidant,
transparency, elasticity and hydrophobicity. Int. J. Biol. Macromol. 2018;115:438–446. doi: 10.1016/j.ijbiomac.2018.04.040. [PubMed] [CrossRef] [Google Scholar]103.
Qiu
J., Niu X., Wang J., Xing Y., Leng B., Dong J., Li H., Luo M., Zhang
Y., Dai X. Capsaicin protects mice from community-associated
methicillin-resistant Staphylococcus aureus pneumonia. PLoS ONE. 2012;7:e33032. doi: 10.1371/journal.pone.0033032. [PMC free article] [PubMed] [CrossRef] [Google Scholar]105.
Jespersen M.G., Lacey J.A., Tong S.Y.C., Davies M.R. Global genomic epidemiology of Streptococcus pyogenes. Infect. Genet. Evol. 2020;86:104609. doi: 10.1016/j.meegid.2020.104609. [PubMed] [CrossRef] [Google Scholar]106.
Lynskey N.N., Lawrenson R.A., Sriskandan S. New understandings in Streptococcus pyogenes. Curr. Opin. Infect. Dis. 2011;24:196–202. doi: 10.1097/QCO.0b013e3283458f7e. [PubMed] [CrossRef] [Google Scholar]107.
González-Abad M.J., Alonso Sanz M. Infecciones invasoras por Streptococcus pyogenes (2011–2018): Serotipos y presentación clínica. An. Pediatría. 2020;92:351–358. doi: 10.1016/j.anpedi.2019.10.014. [PubMed] [CrossRef] [Google Scholar]108.
Sriskandan S., Faulkner L., Hopkins P. Streptococcus pyogenes: Insight into the function of the streptococcal superantigens. Int. J. Biochem. Cell Biol. 2007;39:12–19. doi: 10.1016/j.biocel.2006.08.009. [PubMed] [CrossRef] [Google Scholar]109.
Alouf J.E. Streptococcal toxins (streptolysin O, streptolysin S, erythrogenic toxin) Pharmacol. Ther. 1980;11:661–717. doi: 10.1016/0163-7258(80)90045-5. [PubMed] [CrossRef] [Google Scholar]110.
Noskin G.A., Peterson L.R., Warren J.R. Enterococcus faecium and Enterococcus faecalis bacteremia: Acquisition and outcome. Clin. Infect. Dis. 1995;20:296–301. doi: 10.1093/clinids/20.2.296. [PubMed] [CrossRef] [Google Scholar]111.
Schaberg D.R., Culver D.H., Gaynes R.P. Major trends in the microbial etiology of nosocomial infection. Am. J. Med. 1991;91:S72–S75. doi: 10.1016/0002-9343(91)90346-Y. [PubMed] [CrossRef] [Google Scholar]112.
Kaye D. Enterococci: Biologic and epidemiologic characteristics and in vitro susceptibility. Arch. Intern. Med. 1982;142:2006–2009. doi: 10.1001/archinte.1982.00340240028006. [PubMed] [CrossRef] [Google Scholar]113.
Maki D.G., Agger W.A. Enterococcal Bacteremia: Clinical Features, the Risk of Endocarditis, and Management. Medicine. 1988;67:248. doi: 10.1097/00005792-198807000-00005. [PubMed] [CrossRef] [Google Scholar]115.
Flagan S.F., Leadbetter J.R. Utilization of capsaicin and vanillylamine as growth substrates by Capsicum (hot pepper)-associated bacteria. Environ. Microbiol. 2006;8:560–565. doi: 10.1111/j.1462-2920.2005.00938.x. [PubMed] [CrossRef] [Google Scholar]116.
Gu H.J., Sun Q.L., Luo J.C., Zhang J., Sun L. A First Study of the Virulence Potential of a Bacillus subtilis Isolate from Deep-Sea Hydrothermal Vent. Front. Cell Infect. Microbiol. 2019;9:183. doi: 10.3389/fcimb.2019.00183. [PMC free article] [PubMed] [CrossRef] [Google Scholar]117.
Brown K.L. Control of bacterial spores. Br. Med. Bull. 2000;56:158–171. doi: 10.1258/0007142001902860. [PubMed] [CrossRef] [Google Scholar]118.
Cote C.K., Heffron J.D., Bozue J.A., Welkos S.L. Chapter 102—Bacillus anthracis and Other Bacillus Species. In: Tang Y.-W., Sussman M., Liu D., Poxton I., Schwartzman J., editors. Molecular Medical Microbiology. 2nd ed. Academic Press; Boston, MA, USA: 2015. pp. 1789–1844. [CrossRef] [Google Scholar]120.
Molina-
Torres J., García-Chávez A., Ramírez-Chávez E. Antimicrobial properties
of alkamides present in flavouring plants traditionally used in
Mesoamerica: Affinin and capsaicin. J. Ethnopharmacol. 1999;64:241–248. doi: 10.1016/S0378-8741(98)00134-2. [PubMed] [CrossRef] [Google Scholar]121.
Argôlo-Filho R.C., Loguercio L.L. Bacillus
thuringiensis Is an Environmental Pathogen and Host-Specificity Has
Developed as an Adaptation to Human-Generated Ecological Niches. Insects. 2013;5:62–91. doi: 10.3390/insects5010062. [PMC free article] [PubMed] [CrossRef] [Google Scholar]123.
Schwarzkopf A. Listeria monocytogenes–aspects of pathogenicity. Pathol. Biol. 1996;44:769–774. [PubMed] [Google Scholar]124.
Disson O., Moura A., Lecuit M. Making Sense of the Biodiversity and Virulence of Listeria monocytogenes. Trends Microbiol. 2021;29:811–822. doi: 10.1016/j.tim.2021.01.008. [PubMed] [CrossRef] [Google Scholar]125.
Colwell R.R., Kaper J., Joseph S.W. Vibrio cholerae, Vibrio parahaemolyticus, and other vibrios: Occurrence and distribution in Chesapeake Bay. Science. 1977;198:394–396. [PubMed] [Google Scholar]126.
Garay E., Arnau A., Amaro C. Incidence of Vibrio cholerae and related vibrios in a coastal lagoon and seawater influenced by lake discharges along an annual cycle. Appl. Environ. Microbiol. 1985;50:426–430. doi: 10.1128/aem.50.2.426-430.1985. [PMC free article] [PubMed] [CrossRef] [Google Scholar]127.
Reidl J., Klose K.E. Vibrio cholerae and cholera: Out of the water and into the host. FEMS Microbiol. Rev. 2002;26:125–139. doi: 10.1111/j.1574-6976.2002.tb00605.x. [PubMed] [CrossRef] [Google Scholar]128.
Glass R.I., Huq I., Alim A.R., Yunus M. Emergence of multiply antibiotic-resistant Vibrio cholerae in Bangladesh. J. Infect. Dis. 1980;142:939–942. doi: 10.1093/infdis/142.6.939. [PubMed] [CrossRef] [Google Scholar]129.
Das B., Verma J., Kumar P., Ghosh A., Ramamurthy T. Antibiotic resistance in Vibrio cholerae: Understanding the ecology of resistance genes and mechanisms. Vaccine. 2020;38((Suppl. S1)):A83–A92. doi: 10.1016/j.vaccine.2019.06.031. [PubMed] [CrossRef] [Google Scholar]130.
Alam
M., Islam M.T., Rashed S.M., Johura F.T., Bhuiyan N.A., Delgado G.,
Morales R., Mendez J.L., Navarro A., Watanabe H., et al. Vibrio cholerae classical biotype strains reveal distinct signatures in Mexico. J. Clin. Microbiol. 2012;50:2212–2216. doi: 10.1128/JCM.00189-12. [PMC free article] [PubMed] [CrossRef] [Google Scholar]131.
Asif M., Alvi I.A., Rehman S.U. Insight into Acinetobacter baumannii: Pathogenesis, global resistance, mechanisms of resistance, treatment options, and alternative modalities. Infect. Drug Resist. 2018;11:1249–1260. doi: 10.2147/IDR.S166750. [PMC free article] [PubMed] [CrossRef] [Google Scholar]132.
Pourhajibagher M., Hashemi F.B., Pourakbari B., Aziemzadeh M., Bahador A. Antimicrobial Resistance of Acinetobacter baumannii to Imipenem in Iran: A Systematic Review and Meta-Analysis. Open Microbiol. J. 2016;10:32–42. doi: 10.2174/1874285801610010032. [PMC free article] [PubMed] [CrossRef] [Google Scholar]133.
Qi
L., Li H., Zhang C., Liang B., Li J., Wang L., Du X., Liu X., Qiu S.,
Song H. Relationship between Antibiotic Resistance, Biofilm Formation,
and Biofilm-Specific Resistance in Acinetobacter baumannii. Front. Microbiol. 2016;7:483. doi: 10.3389/fmicb.2016.00483. [PMC free article] [PubMed] [CrossRef] [Google Scholar]134.
Gheorghe-
Barbu I., Barbu I.C., Popa L.I., Pîrcălăbioru G.G., Popa M., Măruțescu
L., Niță-Lazar M., Banciu A., Stoica C., Gheorghe Ș., et al.
Temporo-spatial variations in resistance determinants and clonality of Acinetobacter baumannii and Pseudomonas aeruginosa strains from Romanian hospitals and wastewaters. Antimicrob. Resist. Infect. Control. 2022;11:115. doi: 10.1186/s13756-022-01156-1. [PMC free article] [PubMed] [CrossRef] [Google Scholar]135.
Guo
T., Li M., Sun X., Wang Y., Yang L., Jiao H., Li G. Synergistic
Activity of Capsaicin and Colistin against Colistin-Resistant Acinetobacter baumannii: In Vitro/Vivo Efficacy and Mode of Action. Front. Pharmacol. 2021;12:744494. doi: 10.3389/fphar.2021.744494. [PMC free article] [PubMed] [CrossRef] [Google Scholar]136.
Mégraud F. Resistance of Helicobacter pylori to antibiotics and its impact on treatment options. Drug Resist. Updat. 2001;4:178–186. doi: 10.1054/drup.2001.0203. [PubMed] [CrossRef] [Google Scholar]137.
Dascălu R., Bolocan A., Păduaru D., Constantinescu A., Mitache M., Stoica A., Andronic O. Multidrug resistance in Helicobacter pylori infection. Front. Microbiol. 2023;14:1128497. doi: 10.3389/fmicb.2023.1128497. [PMC free article] [PubMed] [CrossRef] [Google Scholar]138.
Jones N.L., Shabib S., Sherman P.M. Capsaicin as an inhibitor of the growth of the gastric pathogen Helicobacter pylori. FEMS Microbiol. Lett. 1997;146:223–227. doi: 10.1111/j.1574-6968.1997.tb10197.x. [PubMed] [CrossRef] [Google Scholar]139.
Saha
K., Sarkar D., Khan U., Karmakar B.C., Paul S., Mukhopadhyay A.K.,
Dutta S., Bhattacharya S. Capsaicin Inhibits Inflammation and Gastric
Damage during H pylori Infection by Targeting NF-kB-miRNA Axis. Pathogens. 2022;11:641. doi: 10.3390/pathogens11060641. [PMC free article] [PubMed] [CrossRef] [Google Scholar]140.
Venier
N.A., Colquhoun A.J., Sasaki H., Kiss A., Sugar L., Adomat H., Fleshner
N.E., Klotz L.H., Venkateswaran V. Capsaicin: A novel radio-sensitizing
agent for prostate cancer. Prostate. 2015;75:113–125. doi: 10.1002/pros.22896. [PubMed] [CrossRef] [Google Scholar]143.
Allerberger
F., Liesegang A., Grif K., Khaschabi D., Prager R., Danzl J., Höck F.,
Ottl J., Dierich M.P., Berghold C., et al. Occurrence of Salmonella enterica serovar Dublin in Austria. Wien Med. Wochenschr. 2003;153:148–152. doi: 10.1046/j.1563-258X.2003.03015.x. [PubMed] [CrossRef] [Google Scholar]144.
Elias A., Viana J.X., Rangel H., Osles A.G. Antigenic variation in Salmonella typhimurium. Proc. Soc. Exp. Biol. Med. 1974;145:392–396. doi: 10.3181/00379727-145-37817. [PubMed] [CrossRef] [Google Scholar]145.
Martin
L.J., Fyfe M., Doré K., Buxton J.A., Pollari F., Henry B., Middleton
D., Ahmed R., Jamieson F., Ciebin B., et al. Increased Burden of Illness
Associated with Antimicrobial-Resistant Salmonella enterica Serotype Typhimurium Infections. J. Infect. Dis. 2004;189:377–384. doi: 10.1086/381270. [PubMed] [CrossRef] [Google Scholar]146.
Hussain A., Satti L., Hanif F., Zehra N.M., Nadeem S., Bangash T.M., Peter A. Typhoidal Salmonella strains in Pakistan: An impending threat of extensively drug-resistant Salmonella Typhi. Eur. J. Clin. Microbiol. Infect. Dis. 2019;38:2145–2149. doi: 10.1007/s10096-019-03658-0. [PubMed] [CrossRef] [Google Scholar]147.
Butaye P., Michael G.B., Schwarz S., Barrett T.J., Brisabois A., White D.G. The clonal spread of multidrug-resistant non-typhi Salmonella serotypes. Microbes Infect. 2006;8:1891–1897. doi: 10.1016/j.micinf.2005.12.020. [PubMed] [CrossRef] [Google Scholar]148.
Chiu
C.H., Wu T.L., Su L.H., Chu C., Chia J.H., Kuo A.J., Chien M.S., Lin
T.Y. The emergence in Taiwan of fluoroquinolone resistance in Salmonella enterica serotype choleraesuis. N. Engl. J. Med. 2002;346:413–419. doi: 10.1056/NEJMoa012261. [PubMed] [CrossRef] [Google Scholar]149.
Kaper J.B., Nataro J.P., Mobley H.L. Pathogenic Escherichia coli. Nat. Rev. Microbiol. 2004;2:123–140. doi: 10.1038/nrmicro818. [PubMed] [CrossRef] [Google Scholar]150.
Gomes T.A., Elias W.P., Scaletsky I.C., Guth B.E., Rodrigues J.F., Piazza R.M., Ferreira L.C., Martinez M.B. Diarrheagenic Escherichia coli. Braz. J. Microbiol. 2016;47((Suppl. S1)):3–30. doi: 10.1016/j.bjm.2016.10.015. [PMC free article] [PubMed] [CrossRef] [Google Scholar]151.
Cerceo
E., Deitelzweig S.B., Sherman B.M., Amin A.N. Multidrug-Resistant
Gram-Negative Bacterial Infections in the Hospital Setting: Overview,
Implications for Clinical Practice, and Emerging Treatment Options. Microb. Drug Resist. 2016;22:412–431. doi: 10.1089/mdr.2015.0220. [PubMed] [CrossRef] [Google Scholar]152.
Zhang Y., Yang J., Ye L., Luo Y., Wang W., Zhou W., Cui Z., Han L. Characterization of clinical multidrug-resistant Escherichia coli and Klebsiella pneumoniae isolates, 2007–2009, China. Microb. Drug Resist. 2012;18:465–470. doi: 10.1089/mdr.2012.0016. [PubMed] [CrossRef] [Google Scholar]153.
Navon-Venezia S., Kondratyeva K., Carattoli A. Klebsiella pneumoniae: A major worldwide source and shuttle for antibiotic resistance. FEMS Microbiol. Rev. 2017;41:252–275. doi: 10.1093/femsre/fux013. [PubMed] [CrossRef] [Google Scholar]154.
Effah C.Y., Sun T., Liu S., Wu Y. Klebsiella pneumoniae: An increasing threat to public health. Ann. Clin. Microbiol. Antimicrob. 2020;19:1. doi: 10.1186/s12941-019-0343-8. [PMC free article] [PubMed] [CrossRef] [Google Scholar]155.
Podschun R., Ullmann U. Klebsiella spp. as nosocomial pathogens: Epidemiology, taxonomy, typing methods, and pathogenicity factors. Clin. Microbiol. Rev. 1998;11:589–603. doi: 10.1128/CMR.11.4.589. [PMC free article] [PubMed] [CrossRef] [Google Scholar]156.
Surleac
M., Czobor Barbu I., Paraschiv S., Popa L.I., Gheorghe I., Marutescu
L., Popa M., Sarbu I., Talapan D., Nita M., et al. Whole genome
sequencing snapshot of multi-drug resistant Klebsiella pneumoniae strains from hospitals and receiving wastewater treatment plants in Southern Romania. PLoS ONE. 2020;15:e0228079. doi: 10.1371/journal.pone.0228079. [PMC free article] [PubMed] [CrossRef] [Google Scholar]157.
Hassan
M.G., Abdulrazik G., El Awady M.E., Hamed A.A., Abdel-Monem M.O.
Antimicrobial Activity of Capsaicin and Its Derivatives against Klebsiella pneumoniae. Egypt. Acad. J. Biol. Sci. G. Microbiol. 2021;13:79–90. doi: 10.21608/eajbsg.2021.211278. [CrossRef] [Google Scholar]158.
Al-
Musawi S., Albukhaty S., Al-Karagoly H., Sulaiman G.M., Alwahibi M.S.,
Dewir Y.H., Soliman D.A., Rizwana H. Antibacterial Activity of
Honey/Chitosan Nanofibers Loaded with Capsaicin and Gold Nanoparticles
for Wound Dressing. Molecules. 2020;25:4770. doi: 10.3390/molecules25204770. [PMC free article] [PubMed] [CrossRef] [Google Scholar]159.
Papazafiropoulou
A., Daniil I., Sotiropoulos A., Balampani E., Kokolaki A., Bousboulas
S., Konstantopoulou S., Skliros E., Petropoulou D., Pappas S. Prevalence
of asymptomatic bacteriuria in type 2 diabetic subjects with and
without microalbuminuria. BMC Res. Notes. 2010;3:169. doi: 10.1186/1756-0500-3-169. [PMC free article] [PubMed] [CrossRef] [Google Scholar]160.
Matthews S.J., Lancaster J.W. Urinary tract infections in the elderly population. Am. J. Geriatr. Pharmacother. 2011;9:286–309. doi: 10.1016/j.amjopharm.2011.07.002. [PubMed] [CrossRef] [Google Scholar]161.
Rodriguez-Mañas L. Urinary tract infections in the elderly: A review of disease characteristics and current treatment options. Drugs Context. 2020;9:2020-4-13. doi: 10.7573/dic.2020-4-13. [PMC free article] [PubMed] [CrossRef] [Google Scholar]163.
Mobley H.L., Warren J.W. Urease-positive bacteriuria and obstruction of long-term urinary catheters. J. Clin. Microbiol. 1987;25:2216–2217. doi: 10.1128/jcm.25.11.2216-2217.1987. [PMC free article] [PubMed] [CrossRef] [Google Scholar]164.
Mulvey M.A., Klumpp D.J., Stapleton A.E. Urinary Tract Infections: Molecular Pathogenesis and Clinical Management. Wiley; Hoboken, NJ, USA: 2020. [Google Scholar]165.
Hall R.M., Collis C.M. Antibiotic resistance in gram-negative bacteria: The role of gene cassettes and integrons. Drug Resist. Updat. 1998;1:109–119. doi: 10.1016/S1368-7646(98)80026-5. [PubMed] [CrossRef] [Google Scholar]166.
Tumbarello
M., Trecarichi E.M., Fiori B., Losito A.R., D’Inzeo T., Campana L.,
Ruggeri A., Di Meco E., Liberto E., Fadda G., et al. Multidrug-resistant
Proteus mirabilis bloodstream infections: Risk factors and outcomes. Antimicrob. Agents Chemother. 2012;56:3224–3231. doi: 10.1128/AAC.05966-11. [PMC free article] [PubMed] [CrossRef] [Google Scholar]167.
Pagani
L., Migliavacca R., Pallecchi L., Matti C., Giacobone E., Amicosante
G., Romero E., Rossolini G.M. Emerging extended-spectrum beta-lactamases
in Proteus mirabilis. J. Clin. Microbiol. 2002;40:1549–1552. doi: 10.1128/JCM.40.4.1549-1552.2002. [PMC free article] [PubMed] [CrossRef] [Google Scholar]168.
Endimiani A., Luzzaro F., Brigante G., Perilli M., Lombardi G., Amicosante G., Rossolini G.M., Toniolo A. Proteus mirabilis bloodstream infections: Risk factors and treatment outcome related to the expression of extended-spectrum beta-lactamases. Antimicrob. Agents Chemother. 2005;49:2598–2605. doi: 10.1128/AAC.49.7.2598-2605.2005. [PMC free article] [PubMed] [CrossRef] [Google Scholar]169.
Cohen-Nahum K., Saidel-Odes L., Riesenberg K., Schlaeffer F., Borer A. Urinary tract infections caused by multi-drug resistant Proteus mirabilis: Risk factors and clinical outcomes. Infection. 2010;38:41–46. doi: 10.1007/s15010-009-8460-5. [PubMed] [CrossRef] [Google Scholar]170.
D’Andrea
M.M., Literacka E., Zioga A., Giani T., Baraniak A., Fiett J., Sadowy
E., Tassios P.T., Rossolini G.M., Gniadkowski M., et al. Evolution and
spread of a multidrug-resistant Proteus mirabilis clone with chromosomal AmpC-type cephalosporinases in Europe. Antimicrob. Agents Chemother. 2011;55:2735–2742. doi: 10.1128/AAC.01736-10. [PMC free article] [PubMed] [CrossRef] [Google Scholar]171.
Charkhian
H., Bodaqlouie A., Soleimannezhadbari E., Lotfollahi L., Shaykh-Baygloo
N., Hosseinzadeh R., Yousefi N., Khodayar M. Comparing the
Bacteriostatic Effects of Different Metal Nanoparticles against Proteus vulgaris. Curr. Microbiol. 2020;77:2674–2684. doi: 10.1007/s00284-020-02029-9. [PubMed] [CrossRef] [Google Scholar]173.
Buhl
M., Peter S., Willmann M. Prevalence and risk factors associated with
colonization and infection of extensively drug-resistant Pseudomonas aeruginosa: A systematic review. Expert Rev. Anti. Infect. Ther. 2015;13:1159–1170. doi: 10.1586/14787210.2015.1064310. [PubMed] [CrossRef] [Google Scholar]174.
Murphy T.F. Pseudomonas aeruginosa in adults with chronic obstructive pulmonary disease. Curr. Opin. Pulm. Med. 2009;15:138–142. doi: 10.1097/MCP.0b013e328321861a. [PubMed] [CrossRef] [Google Scholar]175.
Gonçalves-
de-Albuquerque C.F., Silva A.R., Burth P., Rocco P.R., Castro-Faria
M.V., Castro-Faria-Neto H.C. Possible mechanisms of Pseudomonas aeruginosa-associated lung disease. Int. J. Med. Microbiol. 2016;306:20–28. doi: 10.1016/j.ijmm.2015.11.001. [PubMed] [CrossRef] [Google Scholar]176.
Talwalkar J.S., Murray T.S. The Approach to Pseudomonas aeruginosa in Cystic Fibrosis. Clin. Chest Med. 2016;37:69–81. doi: 10.1016/j.ccm.2015.10.004. [PubMed] [CrossRef] [Google Scholar]177.
Hancock R.E. Resistance mechanisms in Pseudomonas aeruginosa and other nonfermentative gram-negative bacteria. Clin. Infect. Dis. 1998;27((Suppl. S1)):S93–S99. doi: 10.1086/514909. [PubMed] [CrossRef] [Google Scholar]178.
Pang Z., Raudonis R., Glick B.R., Lin T.J., Cheng Z. Antibiotic resistance in Pseudomonas aeruginosa: Mechanisms and alternative therapeutic strategies. Biotechnol. Adv. 2019;37:177–192. doi: 10.1016/j.biotechadv.2018.11.013. [PubMed] [CrossRef] [Google Scholar]179.
Brown G.D., Denning D.W., Levitz S.M. Tackling Human Fungal Infections. Science. 2012;336:647. doi: 10.1126/science.1222236. [PubMed] [CrossRef] [Google Scholar]180.
Rodriguez-
Tudela J., Alastruey-Izquierdo A., Gago S., Cuenca-Estrella M., León C.,
Miro J., Boluda A.N., Camps I.R., Sole A., Denning D. Burden of serious
fungal infections in Spain. Clin. Microbiol. Infect. 2015;21:183–189. doi: 10.1016/j.cmi.2014.07.013. [PubMed] [CrossRef] [Google Scholar]183.
Fisher
M.C., Hawkins N.J., Sanglard D., Gurr S.J. Worldwide emergence of
resistance to antifungal drugs challenges human health and food
security. Science. 2018;360:739–742. doi: 10.1126/science.aap7999. [PubMed] [CrossRef] [Google Scholar]184.
Revie N.M., Iyer K.R., Robbins N., Cowen L.E. Antifungal drug resistance: Evolution, mechanisms and impact. Curr. Opin. Microbiol. 2018;45:70–76. doi: 10.1016/j.mib.2018.02.005. [PMC free article] [PubMed] [CrossRef] [Google Scholar]185.
Ben-Ami R., Kontoyiannis D.P. Resistance to antifungal drugs. Infect. Dis. Clin. 2021;35:279–311. doi: 10.1016/j.idc.2021.03.003. [PubMed] [CrossRef] [Google Scholar]186.
Elewski B.E. Mechanisms of action of systemic antifungal agents. J. Am. Acad. Dermatol. 1993;28:S28–S34. doi: 10.1016/S0190-9622(09)80305-8. [PubMed] [CrossRef] [Google Scholar]187.
Dixon D.M., Walsh T.J. Medical Microbiology. 4th ed. University of Texas Medical Branch at Galveston; Galveston, TX, USA: 1996. Antifungal agents. [PubMed] [Google Scholar]188.
Gupta A.K., Tomas E. New antifungal agents. Dermatol. Clin. 2003;21:565–576. doi: 10.1016/S0733-8635(03)00024-X. [PubMed] [CrossRef] [Google Scholar]189.
Menezes
R.P., Bessa M.A.S., Siqueira C.P., Teixeira S.C., Ferro E.A.V., Martins
M.M., Cunha L.C.S., Martins C.H.G. Antimicrobial, Antivirulence, and
Antiparasitic Potential of Capsicum chinense Jacq. Extracts and Their Isolated Compound Capsaicin. Antibiotics. 2022;11:1154. doi: 10.3390/antibiotics11091154. [PMC free article] [PubMed] [CrossRef] [Google Scholar]190.
Buitimea-
Cantúa G.V., Buitimea-Cantúa N.E., Rocha-Pizaña M.d.R.,
Hernández-Morales A., Magaña-Barajas E., Molina-Torres J. Inhibitory
effect of Capsicum chinense and Piper nigrum fruits, capsaicin and piperine on aflatoxins production in Aspergillus parasiticus by downregulating the expression of afl D, afl M, afl R, and afl S genes of aflatoxins biosynthetic pathway. J. Environ. Sci. Health Part B. 2020;55:835–843. doi: 10.1080/03601234.2020.1787758. [PubMed] [CrossRef] [Google Scholar]191.
Buitimea-
Cantúa G.V., Velez-Haro J.M., Buitimea-Cantúa N.E., Molina-Torres J.,
Rosas-Burgos E.C. GC-EIMS analysis, antifungal and anti-aflatoxigenic
activity of Capsicum chinense and Piper nigrum fruits and their bioactive compounds capsaicin and piperine upon Aspergillus parasiticus. Nat. Prod. Res. 2020;34:1452–1455. doi: 10.1080/14786419.2018.1514395. [PubMed] [CrossRef] [Google Scholar]192.
Millsop J.W., Fazel N. Oral candidiasis. Clin. Dermatol. 2016;34:487–494. doi: 10.1016/j.clindermatol.2016.02.022. [PubMed] [CrossRef] [Google Scholar]194.
Sobel J.D. Vulvovaginal candidosis. Lancet. 2007;369:1961–1971. doi: 10.1016/S0140-6736(07)60917-9. [PubMed] [CrossRef] [Google Scholar]196.
Fidel P.L., Jr. History and new insights into host defense against vaginal candidiasis. Trends Microbiol. 2004;12:220–227. doi: 10.1016/j.tim.2004.03.006. [PubMed] [CrossRef] [Google Scholar]197.
Pappas
P.G., Kauffman C.A., Andes D., Benjamin D.K., Jr., Calandra T.F.,
Edwards J.E., Jr., Filler S.G., Fisher J.F., Kullberg B.-J., Zeichner
L.O., et al. Clinical Practice Guidelines for the Management
Candidiasis: 2009 Update by the Infectious Diseases Society of America. Clin. Infect. Dis. 2009;48:503–535. doi: 10.1086/596757. [PMC free article] [PubMed] [CrossRef] [Google Scholar]198.
Pfaller M.A., Diekema D.J. Epidemiology of invasive candidiasis: A persistent public health problem. Clin. Microbiol. Rev. 2007;20:133–163. doi: 10.1128/CMR.00029-06. [PMC free article] [PubMed] [CrossRef] [Google Scholar]199.
Pfaller M.A., Diekema D.J. Epidemiology of invasive mycoses in North America. Crit. Rev. Microbiol. 2010;36:1–53. doi: 10.3109/10408410903241444. [PubMed] [CrossRef] [Google Scholar]200.
Behbehani
J.M., Irshad M., Shreaz S., Karched M. Anticandidal Activity of
Capsaicin and Its Effect on Ergosterol Biosynthesis and Membrane
Integrity of Candida albicans. Int. J. Mol. Sci. 2023;24:1046. doi: 10.3390/ijms24021046. [PMC free article] [PubMed] [CrossRef] [Google Scholar]201.
Georgianna D.R., Payne G.A. Genetic regulation of aflatoxin biosynthesis: From gene to genome. Fungal Genet. Biol. 2009;46:113–125. doi: 10.1016/j.fgb.2008.10.011. [PubMed] [CrossRef] [Google Scholar]202.
Astoreca A., Vaamonde G., Dalcero A., Ramos A.J., Marín S. Modelling the effect of temperature and water activity of Aspergillus flavus isolates from corn. Int. J. Food Microbiol. 2012;156:60–67. doi: 10.1016/j.ijfoodmicro.2012.03.002. [PubMed] [CrossRef] [Google Scholar]203.
Nikolić M., Savić I., Nikolić A., Jauković M., Kandić V., Stevanović M., Stanković S. Toxigenic species Aspergillus parasiticus originating from Maize Kernels grown in Serbia. Toxins. 2021;13:847. doi: 10.3390/toxins13120847. [PMC free article] [PubMed] [CrossRef] [Google Scholar]204.
Sebők F., Dobolyi C., Zágoni D., Risa A., Krifaton C., Hartman M., Cserháti M., Szoboszlay S., Kriszt B. Aflatoxigenic Aspergillus flavus and Aspergillus parasiticus strains in Hungarian maize fields. Acta Microbiol. Immunol. Hung. 2016;63:491–502. doi: 10.1556/030.63.2016.012. [PubMed] [CrossRef] [Google Scholar]205.
Hernández-
Téllez C.N., Luque-Alcaraz A.G., Núñez-Mexía S.A., Cortez-Rocha M.O.,
Lizardi-Mendoza J., Rosas-Burgos E.C., Rosas-Durazo A.J., Parra-Vergara
N.V., Plascencia-Jatomea M. Relationship between the Antifungal Activity
of Chitosan-Capsaicin Nanoparticles and the Oxidative Stress Response
on Aspergillus parasiticus. Polymers. 2022;14:2774. doi: 10.3390/polym14142774. [PMC free article] [PubMed] [CrossRef] [Google Scholar]206.
Milder J.E., Walzer P.D., Kilgore G., Rutherford I., Klein M. Clinical features of Strongyloides stercoralis infection in an endemic area of the United States. Gastroenterology. 1981;80:1481–1488. doi: 10.1016/0016-5085(81)90261-4. [PubMed] [CrossRef] [Google Scholar]207.
Marsh K., Snow R.W. Host—Parasite interaction and morbidity in malaria endemic areas. Philos. Trans. R. Soc. London. Ser. B Biol. Sci. 1997;352:1385–1394. doi: 10.1098/rstb.1997.0124. [PMC free article] [PubMed] [CrossRef] [Google Scholar]208.
Barry M.A., Weatherhead J.E., Hotez P.J., Woc-Colburn L. Childhood parasitic infections endemic to the United States. Pediatr. Clin. 2013;60:471–485. doi: 10.1016/j.pcl.2012.12.011. [PubMed] [CrossRef] [Google Scholar]209.
Mata L. Sociocultural Factors in the Control and Prevention of Parasitic Diseases. Rev. Infect. Dis. 1982;4:871–879. doi: 10.1093/4.4.871. [PubMed] [CrossRef] [Google Scholar]210.
Fèvre E.M., Bronsvoort B.M.d.C., Hamilton K.A., Cleaveland S. Animal movements and the spread of infectious diseases. Trends Microbiol. 2006;14:125–131. doi: 10.1016/j.tim.2006.01.004. [PMC free article] [PubMed] [CrossRef] [Google Scholar]211.
Torgerson P.R. One world health: Socioeconomic burden and parasitic disease control priorities. Vet. Parasitol. 2013;195:223–232. doi: 10.1016/j.vetpar.2013.04.004. [PubMed] [CrossRef] [Google Scholar]212.
Torgerson
P.R., de Silva N.R., Fèvre E.M., Kasuga F., Rokni M.B., Zhou X.-N.,
Sripa B., Gargouri N., Willingham A.L., Stein C. The global burden of
foodborne parasitic diseases: An update. Trends Parasitol. 2014;30:20–26. doi: 10.1016/j.pt.2013.11.002. [PubMed] [CrossRef] [Google Scholar]213.
Pisarski K. The global burden of disease of zoonotic parasitic diseases: Top 5 contenders for priority consideration. Trop. Med. Infect. Dis. 2019;4:44. doi: 10.3390/tropicalmed4010044. [PMC free article] [PubMed] [CrossRef] [Google Scholar]214.
Sangster
N., Batterham P., Chapman H.D., Duraisingh M., Le Jambre L., Shirley
M., Upcroft J., Upcroft P. Resistance to antiparasitic drugs: The role
of molecular diagnosis. Int. J. Parasitol. 2002;32:637–653. doi: 10.1016/S0020-7519(01)00365-4. [PubMed] [CrossRef] [Google Scholar]215.
Geary T.G., Thompson D.P. Development of antiparasitic drugs in the 21st century. Vet. Parasitol. 2003;115:167–184. doi: 10.1016/S0304-4017(03)00205-X. [PubMed] [CrossRef] [Google Scholar]216.
Periferakis
A., Caruntu A., Periferakis A.-T., Scheau A.-E., Badarau I.A., Caruntu
C., Scheau C. Availability, Toxicology and Medical Significance of
Antimony. Int. J. Environ. Res. Public Health. 2022;19:4669. doi: 10.3390/ijerph19084669. [PMC free article] [PubMed] [CrossRef] [Google Scholar]217.
Valera-
Vera E.A., Reigada C., Sayé M., Digirolamo F.A., Galceran F., Miranda
M.R., Pereira C.A. Effect of capsaicin on the protozoan parasite Trypanosoma cruzi. FEMS Microbiol. Lett. 2020;367:fnaa194. doi: 10.1093/femsle/fnaa194. [PubMed] [CrossRef] [Google Scholar]219.
Zhang Y., Lai B.S., Juhas M., Zhang Y. Toxoplasma gondii secretory proteins and their role in invasion and pathogenesis. Microbiol. Res. 2019;227:126293. doi: 10.1016/j.micres.2019.06.003. [PubMed] [CrossRef] [Google Scholar]220.
Lima T.S., Lodoen M.B. Mechanisms of human innate immune evasion by Toxoplasma gondii. Front. Cell. Infect. Microbiol. 2019;9:103. doi: 10.3389/fcimb.2019.00103. [PMC free article] [PubMed] [CrossRef] [Google Scholar]221.
Dubey J.P., Lindsay D.S., Speer C.A. Structures of Toxoplasma gondii tachyzoites, bradyzoites, and sporozoites and biology and development of tissue cysts. Clin. Microbiol. Rev. 1998;11:267–299. doi: 10.1128/CMR.11.2.267. [PMC free article] [PubMed] [CrossRef] [Google Scholar]222.
Konstantinovic
N., Guegan H., Stäjner T., Belaz S., Robert-Gangneux F. Treatment of
toxoplasmosis: Current options and future perspectives. Food Waterborne Parasitol. 2019;15:e00036. doi: 10.1016/j.fawpar.2019.e00036. [PMC free article] [PubMed] [CrossRef] [Google Scholar]223.
Dardé M.L., Villena I., Pinon J.M., Beguinot I. Severe toxoplasmosis caused by a Toxoplasma gondii strain with a new isoenzyme type acquired in French Guyana. J. Clin. Microbiol. 1998;36:324. doi: 10.1128/JCM.36.1.324-324.1998. [PMC free article] [PubMed] [CrossRef] [Google Scholar]224.
Silva
L.A., Reis-Cunha J.L., Bartholomeu D.C., Vítor R.W. Genetic
Polymorphisms and Phenotypic Profiles of Sulfadiazine-Resistant and
Sensitive Toxoplasma gondii Isolates Obtained from Newborns with Congenital Toxoplasmosis in Minas Gerais, Brazil. PLoS ONE. 2017;12:e0170689. doi: 10.1371/journal.pone.0170689. [PMC free article] [PubMed] [CrossRef] [Google Scholar]225.
Simarro
P.P., Cecchi G., Paone M., Franco J.R., Diarra A., Ruiz J.A., Fèvre
E.M., Courtin F., Mattioli R.C., Jannin J.G. The Atlas of human African
trypanosomiasis: A contribution to global mapping of neglected tropical
diseases. Int. J. Health Geogr. 2010;9:57. doi: 10.1186/1476-072X-9-57. [PMC free article] [PubMed] [CrossRef] [Google Scholar]226.
Desquesnes M., Dia M.L. Trypanosoma vivax: Mechanical transmission in cattle by one of the most common African tabanids, Atylotus agrestis. Exp. Parasitol. 2003;103:35–43. doi: 10.1016/S0014-4894(03)00067-5. [PubMed] [CrossRef] [Google Scholar]227.
Desquesnes M., Dia M.L. Mechanical transmission of Trypanosoma congolense in cattle by the African tabanid Atylotus agrestis. Exp. Parasitol. 2003;105:226–231. doi: 10.1016/j.exppara.2003.12.014. [PubMed] [CrossRef] [Google Scholar]228.
Bouteille B., Oukem O., Bisser S., Dumas M. Treatment perspectives for human African trypanosomiasis. Fundam. Clin. Pharmacol. 2003;17:171–181. doi: 10.1046/j.1472-8206.2003.00167.x. [PubMed] [CrossRef] [Google Scholar]229.
Baker N., de Koning H.P., Mäser P., Horn D. Drug resistance in African trypanosomiasis: The melarsoprol and pentamidine story. Trends Parasitol. 2013;29:110–118. doi: 10.1016/j.pt.2012.12.005. [PMC free article] [PubMed] [CrossRef] [Google Scholar]230.
Lavanchy
D. Hepatitis B virus epidemiology, disease burden, treatment, and
current and emerging prevention and control measures. J. Viral Hepat. 2004;11:97–107. doi: 10.1046/j.1365-2893.2003.00487.x. [PubMed] [CrossRef] [Google Scholar]231.
Ly
K.N., Xing J., Klevens R.M., Jiles R.B., Ward J.W., Holmberg S.D. The
increasing burden of mortality from viral hepatitis in the United States
between 1999 and 2007. Ann. Intern. Med. 2012;156:271–278. doi: 10.7326/0003-4819-156-4-201202210-00004. [PubMed] [CrossRef] [Google Scholar]232.
Kirk
M.D., Pires S.M., Black R.E., Caipo M., Crump J.A., Devleesschauwer B.,
Döpfer D., Fazil A., Fischer-Walker C.L., Hald T. World Health
Organization estimates of the global and regional disease burden of 22
foodborne bacterial, protozoal, and viral diseases, 2010: A data
synthesis. PLoS Med. 2015;12:e1001921. [PMC free article] [PubMed] [Google Scholar]233.
Savic
M., Penders Y., Shi T., Branche A., Pirçon J.Y. Respiratory syncytial
virus disease burden in adults aged 60 years and older in high-income
countries: A systematic literature review and meta-analysis. Influenza Other Respir. Viruses. 2023;17:e13031. doi: 10.1111/irv.13031. [PMC free article] [PubMed] [CrossRef] [Google Scholar]234.
Manolescu
L., Marinescu P., Sultana C., Temereanca A., Vagu C., Grancea C., Ruta
S. HIV lamivudine resistance mutations in HBV co-infected Romanian
patients. J. Int. AIDS Soc. 2008;11:P182. doi: 10.1186/1758-2652-11-S1-P182. [CrossRef] [Google Scholar]235.
Temereanca
A., Ene L., Sultana C., Manolescu L., Duiculescu D., Ruta S.
Transmitted HIV-1 drug resistance in untreated Romanian patients;
Proceedings of the Infectious Diseases Society of America 2011 Annual
Meeting; Boston, MA, USA. 20–23 October 2011. [Google Scholar]236.
Sultana
C., Oprisan G., Szmal C., Vagu C., Temereanca A., Dinu S., Teleman
M.D., Ruta S. Molecular epidemiology of hepatitis C virus strains from
Romania. J. Gastrointestin. Liver Dis. 2011;20:261–266. [PubMed] [Google Scholar]237.
Lefeuvre P., Moriones E. Recombination as a motor of host switches and virus emergence: Geminiviruses as case studies. Curr. Opin. Virol. 2015;10:14–19. doi: 10.1016/j.coviro.2014.12.005. [PubMed] [CrossRef] [Google Scholar]238.
Bo
Z., Miao Y., Xi R., Gao X., Miao D., Chen H., Jung Y.S., Qian Y., Dai
J. Emergence of a novel pathogenic recombinant virus from Bartha vaccine and variant pseudorabies virus in China. Transbound. Emerg. Dis. 2021;68:1454–1464. doi: 10.1111/tbed.13813. [PubMed] [CrossRef] [Google Scholar]239.
Sultana
C., Casian M., Oprea C., Ianache I., Grancea C., Chiriac D., Ruta S.
Hepatitis B Virus Genotypes and Antiviral Resistance Mutations in
Romanian HIV-HBV Co-Infected Patients. Medicina. 2022;58:531. doi: 10.3390/medicina58040531. [PMC free article] [PubMed] [CrossRef] [Google Scholar]240.
Grossarth-
Maticek R., Frentzel-Beyme R., Kanazir D., Jankovic M., Vetter H.
Reported herpes-virus-infection, fever and cancer incidence in a
prospective study. J. Chronic Dis. 1987;40:967–976. doi: 10.1016/0021-9681(87)90147-0. [PubMed] [CrossRef] [Google Scholar]241.
Parkin D.M., Bray F. The burden of HPV-related cancers. Vaccine. 2006;24:S11–S25. doi: 10.1016/j.vaccine.2006.05.111. [PubMed] [CrossRef] [Google Scholar]242.
Sultana
C., Oprişan G., Teleman M.D., Dinu S., Oprea C., Voiculescu M., Ruta
S., Team H.P. Impact of hepatitis C virus core mutations on the response
to interferon-based treatment in chronic hepatitis C. World J. Gastroenterol. 2016;22:8406. doi: 10.3748/wjg.v22.i37.8406. [PMC free article] [PubMed] [CrossRef] [Google Scholar]243.
Goncalves P.H., Ziegelbauer J., Uldrick T.S., Yarchoan R. Kaposi-sarcoma herpesvirus associated cancers and related diseases. Curr. Opin. HIV AIDS. 2017;12:47. doi: 10.1097/COH.0000000000000330. [PMC free article] [PubMed] [CrossRef] [Google Scholar]244.
Sultana C., Rosca A., Ruta S. Correlation Between miR-125b Expression and Liver Fibrosis in Patients with Chronic Hepatitis C. Hepat. Mon. 2019;19:e84615. doi: 10.5812/hepatmon.84615. [CrossRef] [Google Scholar]246.
Pavel
B., Moroti R., Spataru A., Popescu M.R., Panaitescu A.M., Zagrean A.-M.
Neurological Manifestations of SARS-CoV2 Infection: A Narrative Review.
Brain Sci. 2022;12:1531. doi: 10.3390/brainsci12111531. [PMC free article] [PubMed] [CrossRef] [Google Scholar]247.
Fertig
T.E., Chitoiu L., Terinte-Balcan G., Peteu V.-E., Marta D.,
Gherghiceanu M. The atomic portrait of SARS-CoV-2 as captured by
cryo-electron microscopy. J. Cell. Mol. Med. 2022;26:25–34. doi: 10.1111/jcmm.17103. [PMC free article] [PubMed] [CrossRef] [Google Scholar]249.
Messaoudi
I., Amarasinghe G.K., Basler C.F. Filovirus pathogenesis and immune
evasion: Insights from Ebola virus and Marburg virus. Nat. Rev. Microbiol. 2015;13:663–676. doi: 10.1038/nrmicro3524. [PMC free article] [PubMed] [CrossRef] [Google Scholar]250.
Malvy D., McElroy A.K., de Clerck H., Günther S., van Griensven J. Ebola virus disease. Lancet. 2019;393:936–948. doi: 10.1016/S0140-6736(18)33132-5. [PubMed] [CrossRef] [Google Scholar]251.
Jacob
S.T., Crozier I., Fischer W.A., Hewlett A., Kraft C.S., Vega M.-A.d.L.,
Soka M.J., Wahl V., Griffiths A., Bollinger L. Ebola virus disease. Nat. Rev. Dis. Primers. 2020;6:13. doi: 10.1038/s41572-020-0147-3. [PMC free article] [PubMed] [CrossRef] [Google Scholar]252.
Brunker K., Mollentze N. Rabies virus. Trends Microbiol. 2018;26:886–887. doi: 10.1016/j.tim.2018.07.001. [PubMed] [CrossRef] [Google Scholar]253.
Wunner W.H., Conzelmann K.-K. Rabies. Elsevier; Amsterdam, The Netherlands: 2020. Rabies virus; pp. 43–81. [Google Scholar]254.
Sedighpour
D., Taghizadeh H. The effects of mutation on the drug binding affinity
of Neuraminidase: Case study of Capsaicin using steered molecular
dynamics simulation. J. Mol. Model. 2022;28:36. doi: 10.1007/s00894-021-05005-7. [PubMed] [CrossRef] [Google Scholar]255.
Tang K., Zhang X., Guo Y. Identification of the dietary supplement capsaicin as an inhibitor of Lassa virus entry. Acta. Pharm. Sin. B. 2020;10:789–798. doi: 10.1016/j.apsb.2020.02.014. [PMC free article] [PubMed] [CrossRef] [Google Scholar]256.
Labella A.M., Merel S.E. Influenza. Med. Clin. N. Am. 2013;97:621–645. doi: 10.1016/j.mcna.2013.03.001. [PubMed] [CrossRef] [Google Scholar]258.
Gaitonde D.Y., Moore F.C., Morgan M.K. Influenza: Diagnosis and treatment. Am. Fam. Physician. 2019;100:751–758. [PubMed] [Google Scholar]260.
Chang C., Ramphul K. StatPearls. StatPearls Publishing LLC.; Treasure Island, FL, USA: 2023. Amantadine. [PubMed] [Google Scholar]261.
Palomba E., Castelli V., Renisi G., Bandera A., Lombardi A., Gori A. Antiviral Treatments for Influenza. Semin Respir. Crit. Care Med. 2021;42:859–872. doi: 10.1055/s-0041-1733830. [PubMed] [CrossRef] [Google Scholar]262.
Świerczyńska M., Mirowska-Guzel D.M., Pindelska E. Antiviral Drugs in Influenza. Int. J. Environ. Res. Public Health. 2022;19:3018. doi: 10.3390/ijerph19053018. [PMC free article] [PubMed] [CrossRef] [Google Scholar]263.
Aschenbrenner D.S. Xofluza Now Indicated to Prevent Influenza. Am. J. Nurs. 2021;121:26–27. doi: 10.1097/01.NAJ.0000734116.32090.78. [PubMed] [CrossRef] [Google Scholar]265.
Chang
A.Y., Mann T.S., McFawn P.K., Han L., Dong X., Henry P.J. Investigating
the role of MRGPRC11 and capsaicin-sensitive afferent nerves in the
anti-influenza effects exerted by SLIGRL-amide in murine airways. Respir. Res. 2016;17:62. doi: 10.1186/s12931-016-0378-8. [PMC free article] [PubMed] [CrossRef] [Google Scholar]266.
Günther S., Lenz O. Lassa virus. Crit. Rev. Clin. Lab. Sci. 2004;41:339–390. doi: 10.1080/10408360490497456. [PubMed] [CrossRef] [Google Scholar]267.
Happi A.N., Happi C.T., Schoepp R.J. Lassa fever diagnostics: Past, present, and future. Curr. Opin. Virol. 2019;37:132–138. doi: 10.1016/j.coviro.2019.08.002. [PMC free article] [PubMed] [CrossRef] [Google Scholar]268.
Lukashevich I.S., Paessler S., de la Torre J.C. Lassa virus diversity and feasibility for universal prophylactic vaccine. F1000Res. 2019;8 doi: 10.12688/f1000research.16989.1. [PMC free article] [PubMed] [CrossRef] [Google Scholar]269.
Alcorn J.B. Huastec Mayan Ethnobotany. University of Texas Press; Austin, TX, USA: 1984. [Google Scholar]270.
Jain S. Ethnobotany. Interdiscip. Sci. Rev. 1986;11:285–292. doi: 10.1179/isr.1986.11.3.285. [CrossRef] [Google Scholar]271.
Cotton C.M. Ethnobotany: Principles and Applications. John Wiley & Sons; Hoboken, NJ, USA: 1996. [Google Scholar]272.
Heinrich M. Ethnobotany and its role in drug development. Phytother. Res. Int. J. Devoted Pharmacol. Toxicol. Eval. Nat. Prod. Deriv. 2000;14:479–488. doi: 10.1002/1099-1573(200011)14:7<479::AID-PTR958>3.0.CO;2-2. [PubMed] [CrossRef] [Google Scholar]273.
Petran
M., Dragos D., Gilca M. Historical ethnobotanical review of medicinal
plants used to treat children diseases in Romania (1860s–1970s) J. Ethnobiol. Ethnomedicine. 2020;16:15. doi: 10.1186/s13002-020-00364-6. [PMC free article] [PubMed] [CrossRef] [Google Scholar]274.
Balick M.J., Cox P.A. Plants, People, and Culture: The Science of Ethnobotany. Garland Science; New York, NY, USA: 2020. [Google Scholar]275.
Teow S.-Y., Ali S.A. Synergistic antibacterial activity of Curcumin with antibiotics against Staphylococcus aureus. Pak. J. Pharm. Sci. 2015;28:2109–2114. [PubMed] [Google Scholar]276.
Yun D.G., Lee D.G. Antibacterial activity of curcumin via apoptosis-like response in Escherichia coli. Appl. Microbiol. Biotechnol. 2016;100:5505–5514. doi: 10.1007/s00253-016-7415-x. [PubMed] [CrossRef] [Google Scholar]277.
Gunes
H., Gulen D., Mutlu R., Gumus A., Tas T., Topkaya A.E. Antibacterial
effects of curcumin: An in vitro minimum inhibitory concentration study.
Toxicol. Ind. Health. 2016;32:246–250. doi: 10.1177/0748233713498458. [PubMed] [CrossRef] [Google Scholar]278.
Liao Y., Yao Y., Yu Y., Zeng Y. Enhanced antibacterial activity of curcumin by combination with metal ions. Colloid Interface Sci. Commun. 2018;25:1–6. doi: 10.1016/j.colcom.2018.04.009. [CrossRef] [Google Scholar]279.
Smyth
T., Ramachandran V.N., Smyth W.F. A study of the antimicrobial activity
of selected naturally occurring and synthetic coumarins. Int. J. Antimicrob. Agents. 2009;33:421–426. doi: 10.1016/j.ijantimicag.2008.10.022. [PubMed] [CrossRef] [Google Scholar]280.
Choo
S., Chin V.K., Wong E.H., Madhavan P., Tay S.T., Yong P.V.C., Chong
P.P. Review: Antimicrobial properties of allicin used alone or in
combination with other medications. Folia Microbiol. 2020;65:451–465. doi: 10.1007/s12223-020-00786-5. [PubMed] [CrossRef] [Google Scholar]281.
Lauritano
D., Petruzzi M., Baldoni M. Preliminary protocol for systemic
administration of capsaicin for the treatment of the burning mouth
syndrome. Minerva Stomatol. 2003;52:273–278. [PubMed] [Google Scholar]282.
Laude-
Pagniez E., Leclerc J., Lok C., Chaby G., Arnault J.P. Capsaicin 8%
patch as therapy for neuropathic chronic postsurgical pain after
melanoma excision surgery: A single center case series. JAAD Case Rep. 2022;30:70–75. doi: 10.1016/j.jdcr.2022.09.032. [PMC free article] [PubMed] [CrossRef] [Google Scholar]283.
Yang
S., Liu L., Meng L., Hu X. Capsaicin is beneficial to hyperlipidemia,
oxidative stress, endothelial dysfunction, and atherosclerosis in Guinea
pigs fed on a high-fat diet. Chem. Biol. Interact. 2019;297:1–7. doi: 10.1016/j.cbi.2018.10.006. [PubMed] [CrossRef] [Google Scholar]284.
Chan
T.C., Lee M.S., Huang W.C., Chang W.Y., Krueger J.G., Tsai T.F.
Capsaicin attenuates imiquimod-induced epidermal hyperplasia and
cutaneous inflammation in a murine model of psoriasis. Biomed. Pharmacother. 2021;141:111950. doi: 10.1016/j.biopha.2021.111950. [PubMed] [CrossRef] [Google Scholar]285.
Thán
M., Németh J., Szilvássy Z., Pintér E., Helyes Z., Szolcsányi J.
Systemic anti-inflammatory effect of somatostatin released from
capsaicin-sensitive vagal and sciatic sensory fibres of the rat and
guinea-pig. Eur. J. Pharmacol. 2000;399:251–258. doi: 10.1016/S0014-2999(00)00341-1. [PubMed] [CrossRef] [Google Scholar]286.
Popescu
G.D.A., Scheau C., Badarau I.A., Dumitrache M.D., Caruntu A., Scheau
A.E., Costache D.O., Costache R.S., Constantin C., Neagu M., et al. The
Effects of Capsaicin on Gastrointestinal Cancers. Molecules. 2020;26:94. doi: 10.3390/molecules26010094. [PMC free article] [PubMed] [CrossRef] [Google Scholar]287.
Han
T.H., Park M.K., Nakamura H., Ban H.S. Capsaicin inhibits HIF-1α
accumulation through suppression of mitochondrial respiration in lung
cancer cells. Biomed. Pharmacother. 2022;146:112500. doi: 10.1016/j.biopha.2021.112500. [PubMed] [CrossRef] [Google Scholar]288.
Liu X.-Y., Wei D.-G., Li R.-S. Capsaicin induces ferroptosis of NSCLC by regulating SLC7A11/GPX4 signaling in vitro. Sci. Rep. 2022;12:11996. doi: 10.1038/s41598-022-16372-3. [PMC free article] [PubMed] [CrossRef] [Google Scholar]289.
Que
T., Ren B., Fan Y., Liu T., Hou T., Dan W., Liu B., Wei Y., Lei Y.,
Zeng J., et al. Capsaicin inhibits the migration, invasion and EMT of
renal cancer cells by inducing AMPK/mTOR-mediated autophagy. Chem. Biol. Interact. 2022;366:110043. doi: 10.1016/j.cbi.2022.110043. [PubMed] [CrossRef] [Google Scholar]290.
Scheau
C., Badarau I.A., Caruntu C., Mihai G.L., Didilescu A.C., Constantin
C., Neagu M. Capsaicin: Effects on the Pathogenesis of Hepatocellular
Carcinoma. Molecules. 2019;24:2350. doi: 10.3390/molecules24132350. [PMC free article] [PubMed] [CrossRef] [Google Scholar]291.
Georgescu
S.-R., Sârbu M.-I., Matei C., Ilie M.A., Caruntu C., Constantin C.,
Neagu M., Tampa M. Capsaicin: Friend or Foe in Skin Cancer and Other
Related Malignancies? Nutrients. 2017;9:1365. doi: 10.3390/nu9121365. [PMC free article] [PubMed] [CrossRef] [Google Scholar]292.
Scheau C., Mihai L., Bădărău I., Caruntu C. Emerging applications of some important natural compounds in the field of oncology. Farmacia. 2020;68:984–991. doi: 10.31925/farmacia.2020.6.4. [CrossRef] [Google Scholar]293.
Redington
K.L., Disenhouse T., Strantzas S.C., Gladstone R., Wei C., Tropak M.B.,
Dai X., Manlhiot C., Li J., Redington A.N. Remote cardioprotection by
direct peripheral nerve stimulation and topical capsaicin is mediated by
circulating humoral factors. Basic Res. Cardiol. 2012;107:241. doi: 10.1007/s00395-011-0241-5. [PubMed] [CrossRef] [Google Scholar]294.
Scheau
C., Ilie Ghita M., Grigore O., Mihailescu A., Caruntu A., Mihai L.,
Bădărău I., Boda D., Caruntu C. Modulation of capsaicin-induced
neurogenic vasodilation by acute psychological stress. Farmacia. 2021;69:778–784. doi: 10.31925/farmacia.2021.4.20. [CrossRef] [Google Scholar]295.
Shin M.K., Yang S.-M., Han I.-S. Capsaicin suppresses liver fat accumulation in high-fat diet-induced NAFLD mice. Anim. Cells Syst. 2020;24:214–219. doi: 10.1080/19768354.2020.1810771. [PMC free article] [PubMed] [CrossRef] [Google Scholar]296.
Yu
Q., Wang Y., Yu Y., Li Y., Zhao S., Chen Y., Waqar A.B., Fan J., Liu E.
Expression of TRPV1 in rabbits and consuming hot pepper affects its
body weight. Mol. Biol. Rep. 2012;39:7583–7589. doi: 10.1007/s11033-012-1592-1. [PubMed] [CrossRef] [Google Scholar]297.
Dumitrache
M.D., Jieanu A.S., Scheau C., Badarau I.A., Popescu G.D.A., Caruntu A.,
Costache D.O., Costache R.S., Constantin C., Neagu M., et al.
Comparative effects of capsaicin in chronic obstructive pulmonary
disease and asthma (Review) Exp. Ther. Med. 2021;22:917. doi: 10.3892/etm.2021.10349. [PMC free article] [PubMed] [CrossRef] [Google Scholar]298.
Aguilar-Meléndez A., Vásquez M.A., Katz E., Colorado M.R.H. Los Chiles Que le Dan Sabor al Mundo: Contribuciones Multidisciplinarias. IRD Éditions; Hong Kong, China: 2018. [Google Scholar]299.
Aguilar-Meléndez A., Vásquez-Dávila M.A., Manzanero-Medina G.I., Katz E. Chile (Capsicum spp.) as Food-Medicine Continuum in Multiethnic Mexico. Foods. 2021;10:2502. doi: 10.3390/foods10102502. [PMC free article] [PubMed] [CrossRef] [Google Scholar]300.
Sarwa K. Recent Advances in Ethnobotany. Deep Publication; New Delhi, India: 2021. Chapter 04—Some Indigenous Capsicum Species of India And Their Ethnomedicinal Importance Government of India; pp. 18–21. [Google Scholar]301.
Saleh B.K., Omer A., Teweldemedhin B. Medicinal uses and health benefits of chili pepper (Capsicum spp.): A review. MOJ Food Process Technol. 2018;6:325–328. doi: 10.15406/mojfpt.2018.06.00183. [CrossRef] [Google Scholar]302.
Meghvansi
M.K., Siddiqui S., Khan M.H., Gupta V.K., Vairale M.G., Gogoi H.K.,
Singh L. Naga chilli: A potential source of capsaicinoids with
broad-spectrum ethnopharmacological applications. J. Ethnopharmacol. 2010;132:1–14. doi: 10.1016/j.jep.2010.08.034. [PubMed] [CrossRef] [Google Scholar]303.
Sayanlar
J., Guleyupoglu N., Portenoy R., Ashina S. Trigeminal postherpetic
neuralgia responsive to treatment with capsaicin 8% topical patch: A
case report. J. Headache. Pain. 2012;13:587–589. doi: 10.1007/s10194-012-0467-0. [PMC free article] [PubMed] [CrossRef] [Google Scholar]304.
Zis
P., Apsokardos A., Isaia C., Sykioti P., Vadalouca A. Posttraumatic and
postsurgical neuropathic pain responsive to treatment with capsaicin 8%
topical patch. Pain. Physician. 2014;17:E213–E218. [PubMed] [Google Scholar]305.
Zeidler C., Metze D., Ständer S. Successful treatment of lichen amyloidosis using capsaicin 8% patch. J. Eur. Acad. Dermatol. Venereol. 2016;30:1236–1238. doi: 10.1111/jdv.13165. [PubMed] [CrossRef] [Google Scholar]306.
Kocak
A.O., Dogruyol S., Akbas I., Menekse T.S., Gur S.T.A., Kocak M.B.,
Cekmen B., Orun S., Cakir Z. Comparison of topical capsaicin and topical
piroxicam in the treatment of acute trauma-induced pain: A randomized
double-blind trial. Am. J.. Emerg. Med. 2020;38:1767–1771. doi: 10.1016/j.ajem.2020.05.104. [PubMed] [CrossRef] [Google Scholar]307.
Hoesli R.C., Wingo M.L., Wajsberg B., Bastian R.W. Topical Capsaicin for the Treatment of Sensory Neuropathic Cough. OTO Open. 2021;5:2473974x211065668. doi: 10.1177/2473974X211065668. [PMC free article] [PubMed] [CrossRef] [Google Scholar]308.
Van
Gerven L., Steelant B., Cools L., Callebaut I., Backaert W., de Hoon
J., Ampe E., Talavera K., Hellings P.W. Low-dose capsaicin (0.01 mM)
nasal spray is equally effective as the current standard treatment for
idiopathic rhinitis: A randomized, double-blind, placebo-controlled
trial. J. Allergy Clin. Immunol. 2021;147:397–400.e394. doi: 10.1016/j.jaci.2020.04.054. [PubMed] [CrossRef] [Google Scholar]309.
Vachiramon
V., Tanratana P., Anuntrangsee T., Palakornkitti P., Yeesibsean N.,
Kungvalpivat P., Fabi S. The role of topical capsaicin gel in pain
management during microfocused ultrasound treatment for neck laxity. Ski. Res. Technol. 2023;29:e13240. doi: 10.1111/srt.13240. [PMC free article] [PubMed] [CrossRef] [Google Scholar]310.
Hägermark O., Hökfelt T., Pernow B. Flare and itch induced by substance P in human skin. Nation. 1978;12:13. doi: 10.1111/1523-1747.ep12515092. [PubMed] [CrossRef] [Google Scholar]311.
Bartold
P., Kylstra A., Lawson R. Substance P: An immunohistochemical and
biochemical study in human gingival tissues. A role for neurogenic
inflammation? J. Periodontol. 1994;65:1113–1121. doi: 10.1902/jop.1994.65.12.1113. [PubMed] [CrossRef] [Google Scholar]312.
Figini
M., Emanueli C., Bertrand C., Javdan P., Geppetti P. Evidence that
tachykinins relax the guinea-pig trachea via nitric oxide release and by
stimulation of a septide-insensitive NK1 receptor. Br. J. Pharmacol. 1996;117:1270–1276. doi: 10.1111/j.1476-5381.1996.tb16725.x. [PMC free article] [PubMed] [CrossRef] [Google Scholar]313.
Simone
D.A., Nolano M., Johnson T., Wendelschafer-Crabb G., Kennedy W.R.
Intradermal injection of capsaicin in humans produces degeneration and
subsequent reinnervation of epidermal nerve fibers: Correlation with
sensory function. J. Neurosci. 1998;18:8947–8959. doi: 10.1523/JNEUROSCI.18-21-08947.1998. [PMC free article] [PubMed] [CrossRef] [Google Scholar]314.
Chen
F.X., Wan Q., Fang J., Peng L., Li Q.L., Hu J. The Src1-PGC1α-AP1
complex-dependent secretion of substance P induces inflammation and
apoptosis in encephalomyocarditis virus-infected mice. Cytokine. 2023;165:156186. doi: 10.1016/j.cyto.2023.156186. [PubMed] [CrossRef] [Google Scholar]315.
Johnson
M.B., Suptela S.R., Sipprell S.E., Marriott I. Substance P Exacerbates
the Inflammatory and Pro-osteoclastogenic Responses of Murine
Osteoclasts and Osteoblasts to Staphylococcus aureus. Inflammation. 2023;46:256–269. doi: 10.1007/s10753-022-01731-z. [PMC free article] [PubMed] [CrossRef] [Google Scholar]316.
Arruda-
Vasconcelos R., Chiarelli-Neto V.M., Louzada L.M., Aveiro E.,
Alves-Silva E.G., de-Jesus-Soares A., Ferraz C.C.R., Almeida J.F.A.,
Marciano M.A., Pecorari V.G.A., et al. Quantitative analysis of
culturable bacteria, levels of endotoxins, inflammatory mediators and
substance P in teeth with symptomatic irreversible pulpitis and in teeth
with vital normal pulp tissues. Int. Endod J. 2023;56:827–836. doi: 10.1111/iej.13922. [PubMed] [CrossRef] [Google Scholar]317.
Mehboob
R., Oehme P., Pfaff G. The role of Substance P in the defense line of
the respiratory tract and neurological manifestations post COVID-19
infection. Front. Neurol. 2023;14:1052811. doi: 10.3389/fneur.2023.1052811. [PMC free article] [PubMed] [CrossRef] [Google Scholar]318.
Szolcsányi J., Barthó L. Capsaicin-sensitive afferents and their role in gastroprotection: An update. J. Physiol. Paris. 2001;95:181–188. doi: 10.1016/S0928-4257(01)00023-7. [PubMed] [CrossRef] [Google Scholar]319.
Szolcsányi
J., Helyes Z., Oroszi G., Németh J., Pintér E. Release of somatostatin
and its role in the mediation of the anti-inflammatory effect induced by
antidromic stimulation of sensory fibres of rat sciatic nerve. Br. J. Pharmacol. 1998;123:936–942. doi: 10.1038/sj.bjp.0701685. [PMC free article] [PubMed] [CrossRef] [Google Scholar]320.
Helyes
Z., Thán M., Oroszi G., Pintér E., Németh J., Kéri G., Szolcsányi J.
Anti-nociceptive effect induced by somatostatin released from sensory
nerve terminals and by synthetic somatostatin analogues in the rat. Neurosci. Lett. 2000;278:185–188. doi: 10.1016/S0304-3940(99)00936-2. [PubMed] [CrossRef] [Google Scholar]321.
Pintér E., Helyes Z., Szolcsányi J. Inhibitory effect of somatostatin on inflammation and nociception. Pharmacol. Ther. 2006;112:440–456. doi: 10.1016/j.pharmthera.2006.04.010. [PubMed] [CrossRef] [Google Scholar]322.
László
S., Bátai I.Z., Berkó S., Csányi E., Dombi Á., Pozsgai G., Bölcskei K.,
Botz L., Wagner Ö., Pintér E. Development of Capsaicin-Containing
Analgesic Silicone-Based Transdermal Patches. Pharmaceuticals. 2022;15:1279. doi: 10.3390/ph15101279. [PMC free article] [PubMed] [CrossRef] [Google Scholar]323.
Peck R. Neuropeptides modulating macrophage function. Ann. N. Y. Acad. Sci. 1987;496:264–270. doi: 10.1111/j.1749-6632.1987.tb35774.x. [PubMed] [CrossRef] [Google Scholar]324.
Weinstock J.V., Elliott D. The somatostatin immunoregulatory circuit present at sites of chronic inflammation. Eur. J. Endocrinol. 2000;143:S15–S19. doi: 10.1530/eje.0.143s015. [PubMed] [CrossRef] [Google Scholar]325.
Kao
J.Y., Pierzchala A., Rathinavelu S., Zavros Y., Tessier A., Merchant
J.L. Somatostatin inhibits dendritic cell responsiveness to Helicobacter pylori. Regul. Pept. 2006;134:23–29. doi: 10.1016/j.regpep.2005.11.002. [PubMed] [CrossRef] [Google Scholar]326.
Monaco-
Shawver L., Schwartz L., Tuluc F., Guo C.-J., Lai J.P., Gunnam S.M.,
Kilpatrick L.E., Banerjee P.P., Douglas S.D., Orange J.S. Substance P
inhibits natural killer cell cytotoxicity through the neurokinin-1
receptor. J. Leukoc. Biol. 2010;89:113–125. doi: 10.1189/jlb.0410200. [PMC free article] [PubMed] [CrossRef] [Google Scholar]327.
Froidevaux S., Eberle A.N. Somatostatin analogs and radiopeptides in cancer therapy. Pept. Sci. 2002;66:161–183. doi: 10.1002/bip.10256. [PubMed] [CrossRef] [Google Scholar]328.
Klironomos
S., Notas G., Sfakianaki O., Kiagiadaki F., Xidakis C., Kouroumalis E.
Octreotide modulates the effects on fibrosis of TNF-α, TGF-β and PDGF in
activated rat hepatic stellate cells. Regul. Pept. 2014;188:5–12. doi: 10.1016/j.regpep.2013.11.002. [PubMed] [CrossRef] [Google Scholar]329.
Ayiomamitis
G.D., Notas G., Zaravinos A., Drygiannakis I., Georgiadou M.,
Sfakianaki O., Mastrodimou N., Thermos K., Kouroumalis E. Effects of
octreotide and insulin on colon cancer cellular proliferation and
correlation with hTERT activity. Oncoscience. 2014;1:457. doi: 10.18632/oncoscience.58. [PMC free article] [PubMed] [CrossRef] [Google Scholar]330.
Kouroumalis E., Samonakis D., Notas G. Somatostatin in hepatocellular carcinoma: Experimental and therapeutic implications. Hepatoma Res. 2018;4:34. doi: 10.20517/2394-5079.2018.33. [CrossRef] [Google Scholar]331.
Periferakis
A., Tsigas G., Periferakis A.-T., Badarau I.A., Scheau A.-E., Tampa M.,
Georgescu S.R., Didilescu A.C., Scheau C., Caruntu C. Antitumoral and
Anti-inflammatory Roles of Somatostatin and Its Analogs in
Hepatocellular Carcinoma. Anal. Cell. Pathol. 2021;2021:1840069. doi: 10.1155/2021/1840069. [PMC free article] [PubMed] [CrossRef] [Google Scholar]332.
Kouroumalis
E., Tsomidis I., Voumvouraki A. Is There a Place for Somatostatin
Analogues for the Systemic Treatment of Hepatocellular Carcinoma in the
Immunotherapy Era? Livers. 2022;2:315–335. doi: 10.3390/livers2040024. [CrossRef] [Google Scholar]333.
McLaughlin-Drubin M.E., Munger K. Viruses associated with human cancer. Biochim. Biophys. Acta (BBA) Mol. Basis Dis. 2008;1782:127–150. doi: 10.1016/j.bbadis.2007.12.005. [PMC free article] [PubMed] [CrossRef] [Google Scholar]334.
Georgakilas
A.G., Mosley W.G., Georgakila S., Ziech D., Panayiotidis M.I.
Viral-induced human carcinogenesis: An oxidative stress perspective. Mol. BioSystems. 2010;6:1162–1172. doi: 10.1039/b923958h. [PubMed] [CrossRef] [Google Scholar]335.
Alibek K., Kakpenova A., Mussabekova A., Sypabekova M., Karatayeva N. Role of viruses in the development of breast cancer. Infect. Agents Cancer. 2013;8:32. doi: 10.1186/1750-9378-8-32. [PMC free article] [PubMed] [CrossRef] [Google Scholar]336.
Hatano Y., Ideta T., Hirata A., Hatano K., Tomita H., Okada H., Shimizu M., Tanaka T., Hara A. Virus-Driven Carcinogenesis. Cancers. 2021;13:2625. doi: 10.3390/cancers13112625. [PMC free article] [PubMed] [CrossRef] [Google Scholar]338.
De León A.M., Garcia-Santibanez R., Harrison T.B. Article Topic: Neuropathies Due to Infections and Antimicrobial Treatments. Curr. Treat Options Neurol. 2023:1–17. doi: 10.1007/s11940-023-00756-5. [PMC free article] [PubMed] [CrossRef] [Google Scholar]339.
Peppin J.F., Pappagallo M. Capsaicinoids in the treatment of neuropathic pain: A review. Ther. Adv. Neurol. Disord. 2014;7:22–32. doi: 10.1177/1756285613501576. [PMC free article] [PubMed] [CrossRef] [Google Scholar]340.
Filippi
A., Caruntu C., Gheorghe R.O., Deftu A., Amuzescu B., Ristoiu V.
Catecholamines reduce transient receptor potential vanilloid type 1
desensitization in cultured dorsal root ganglia neurons. J. Physiol. Pharmacol. 2016;67:843–850. [PubMed] [Google Scholar]341.
Mihai
A., Chitimus D.M., Jurcut C., Blajut F.C., Opris-Belinski D., Caruntu
C., Ionescu R., Caruntu A. Comparative Analysis of Hematological and
Immunological Parameters in Patients with Primary Sjögren’s Syndrome and
Peripheral Neuropathy. J. Clin. Med. 2023;12:3672. doi: 10.3390/jcm12113672. [PMC free article] [PubMed] [CrossRef] [Google Scholar]342.
Kazamel M., Stino A.M., Smith A.G. Metabolic syndrome and peripheral neuropathy. Muscle Nerve. 2021;63:285–293. doi: 10.1002/mus.27086. [PubMed] [CrossRef] [Google Scholar]343.
Bucurica
S., Prodan I., Pavalean M., Taubner C., Bucurica A., Socol C., Calin
R., Ionita-Radu F., Jinga M. Association of Vitamin D Deficiency and
Insufficiency with Pathology in Hospitalized Patients. Diagnostics. 2023;13:998. doi: 10.3390/diagnostics13050998. [PMC free article] [PubMed] [CrossRef] [Google Scholar]344.
Kawada
T., Suzuki T., Takahashi M., Iwai K. Gastrointestinal absorption and
metabolism of capsaicin and dihydrocapsaicin in rats. Toxicol. Appl. Pharmacol. 1984;72:449–456. doi: 10.1016/0041-008X(84)90121-2. [PubMed] [CrossRef] [Google Scholar]345.
Sharma S.K., Vij A.S., Sharma M. Mechanisms and clinical uses of capsaicin. Eur. J. Pharmacol. 2013;720:55–62. doi: 10.1016/j.ejphar.2013.10.053. [PubMed] [CrossRef] [Google Scholar]346.
Chanda S., Bashir M., Babbar S., Koganti A., Bley K. In vitro hepatic and skin metabolism of capsaicin. Drug Metab. Dispos. 2008;36:670–675. doi: 10.1124/dmd.107.019240. [PubMed] [CrossRef] [Google Scholar]347.
Qin
L., Wang Y., Gong Y., Chen J., Xu B., Tang L., Guo L., Xie J. Capsaicin
metabolites and GSH-associated detoxification and biotransformation
pathways in human liver microsomes revealed by LC-HRMS/MS with
data-mining tools. J. Chromatogr. B Anal. Technol. Biomed. Life Sci. 2019;1133:121843. doi: 10.1016/j.jchromb.2019.121843. [PubMed] [CrossRef] [Google Scholar]348.
Rollyson
W.D., Stover C.A., Brown K.C., Perry H.E., Stevenson C.D., McNees C.A.,
Ball J.G., Valentovic M.A., Dasgupta P. Bioavailability of capsaicin
and its implications for drug delivery. J. Control. Release. 2014;196:96–105. doi: 10.1016/j.jconrel.2014.09.027. [PMC free article] [PubMed] [CrossRef] [Google Scholar]349.
Babbar
S., Marier J.F., Mouksassi M.S., Beliveau M., Vanhove G.F., Chanda S.,
Bley K. Pharmacokinetic analysis of capsaicin after topical
administration of a high-concentration capsaicin patch to patients with
peripheral neuropathic pain. Ther. Drug Monit. 2009;31:502–510. doi: 10.1097/FTD.0b013e3181a8b200. [PubMed] [CrossRef] [Google Scholar]350.
Zak
A., Siwinska N., Slowikowska M., Borowicz H., Szpot P., Zawadzki M.,
Niedzwiedz A. The detection of capsaicin and dihydrocapsaicin in horse
serum following long-term local administration. BMC Vet. Res. 2018;14:193. doi: 10.1186/s12917-018-1518-9. [PMC free article] [PubMed] [CrossRef] [Google Scholar]351.
Goci
E., Haloci E., Di Stefano A., Chiavaroli A., Angelini P., Miha A.,
Cacciatore I., Marinelli L. Evaluation of In Vitro Capsaicin Release and
Antimicrobial Properties of Topical Pharmaceutical Formulation. Biomolecules. 2021;11:432. doi: 10.3390/biom11030432. [PMC free article] [PubMed] [CrossRef] [Google Scholar]352.
Reilly
C.A., Yost G.S. Metabolism of capsaicinoids by P450 enzymes: A review
of recent findings on reaction mechanisms, bio-activation, and
detoxification processes. Drug Metab. Rev. 2006;38:685–706. doi: 10.1080/03602530600959557. [PMC free article] [PubMed] [CrossRef] [Google Scholar]353.
van
Eijl S., Zhu Z., Cupitt J., Gierula M., Götz C., Fritsche E., Edwards
R.J. Elucidation of xenobiotic metabolism pathways in human skin and
human skin models by proteomic profiling. PLoS ONE. 2012;7:e41721. doi: 10.1371/journal.pone.0041721. [PMC free article] [PubMed] [CrossRef] [Google Scholar]354.
Tian K., Zhu J., Li M., Qiu X. Capsaicin is efficiently transformed by multiple cytochrome P450s from Capsicum fruit-feeding Helicoverpa armigera. Pestic. Biochem. Physiol. 2019;156:145–151. doi: 10.1016/j.pestbp.2019.02.015. [PubMed] [CrossRef] [Google Scholar]355.
Marquez-Algaba E., Burgos J., Almirante B. Pharmacotherapeutic interventions for the treatment of bacterial prostatitis. Expert Opin. Pharmacother. 2022;23:1091–1101. doi: 10.1080/14656566.2022.2077101. [PubMed] [CrossRef] [Google Scholar]356.
Norman
G., Dumville J.C., Mohapatra D.P., Owens G.L., Crosbie E.J. Antibiotics
and antiseptics for surgical wounds healing by secondary intention. Cochrane Database Syst. Rev. 2016;3:Cd011712. doi: 10.1001/jamadermatol.2016.3131. [PMC free article] [PubMed] [CrossRef] [Google Scholar]357.
Dragosloveanu
Ş., Dragosloveanu C.D.M., Stanca H.T., Cotor D.C., Dragosloveanu C.I.,
Stoica C.I. A new perspective towards failure of gamma nail systems. Exp. Ther. Med. 2020;20:216. doi: 10.3892/etm.2020.9346. [PMC free article] [PubMed] [CrossRef] [Google Scholar]358.
Monaghan M.G., Murphy C.M. Old Drugs, New Tricks–Redefining Therapeutic Strategies for Tissue Regeneration. Adv. Drug Deliv. Rev. 2021;173:279–280. doi: 10.1016/j.addr.2021.03.019. [PubMed] [CrossRef] [Google Scholar]359.
Bergren D.R. Capsaicin challenge, reflex bronchoconstriction, and local action of substance P. Am. J. Physiol. 1988;254:R845–R852. doi: 10.1152/ajpregu.1988.254.5.R845. [PubMed] [CrossRef] [Google Scholar]360.
Thomas
K.C., Ethirajan M., Shahrokh K., Sun H., Lee J., Cheatham T.E., 3rd,
Yost G.S., Reilly C.A. Structure-activity relationship of capsaicin
analogs and transient receptor potential vanilloid 1-mediated human lung
epithelial cell toxicity. J. Pharmacol. Exp. Ther. 2011;337:400–410. doi: 10.1124/jpet.110.178491. [PMC free article] [PubMed] [CrossRef] [Google Scholar]361.
Trevisan
G., Rossato M.F., Hoffmeister C., Oliveira S.M., Silva C.R., Matheus
F.C., Mello G.C., Antunes E., Prediger R.D., Ferreira J. Mechanisms
involved in abdominal nociception induced by either TRPV1 or TRPA1
stimulation of rat peritoneum. Eur. J. Pharmacol. 2013;714:332–344. doi: 10.1016/j.ejphar.2013.07.029. [PubMed] [CrossRef] [Google Scholar]363.
Xu
Y., Gu Q., Qu C. Capsaicin pretreatment reversed pulmonary arterial
hypertension by alleviating inflammation via p38MAPK pathway. Exp. Lung Res. 2017;43:8–18. doi: 10.1080/01902148.2016.1271481. [PubMed] [CrossRef] [Google Scholar]364.
Lechner A., Alderson T., Gautam S., Flaker G. Ventricular fibrillation due to coronary spasm after pepper spray. Pacing. Clin. Electrophysiol. 2021;44:548–551. doi: 10.1111/pace.14146. [PubMed] [CrossRef] [Google Scholar]365.
Jancsó G., Király E., Such G., Joó F., Nagy A. Neurotoxic effect of capsaicin in mammals. Acta. Physiol. Hung. 1987;69:295–313. [PubMed] [Google Scholar]366.
Ritter S., Dinh T.T. Capsaicin-induced neuronal degeneration in the brain and retina of preweanling rats. J. Comp. Neurol. 1990;296:447–461. doi: 10.1002/cne.902960310. [PubMed] [CrossRef] [Google Scholar]367.
Forrester
M.B., Holloway C. Characteristics of pepper spray-related injuries
reported to the National Electronic Injury Surveillance System during
2000–2020. Clin. Toxicol. 2022;60:348–355. doi: 10.1080/15563650.2021.1966028. [PubMed] [CrossRef] [Google Scholar]368.
McGilton
K.S., Höbler F., Campos J., Dupuis K., Labreche T., Guthrie D.M., Jarry
J., Singh G., Wittich W. Hearing and vision screening tools for
long-term care residents with dementia: Protocol for a scoping review. BMJ Open. 2016;6:e011945. doi: 10.1136/bmjopen-2016-011945. [PMC free article] [PubMed] [CrossRef] [Google Scholar]369.
Stoica
C.I., Nedelea G., Cotor D.C., Gherghe M., Georgescu D.E., Dragosloveanu
C., Dragosloveanu S. The Outcome of Total Knee Arthroplasty for
Patients with Psychiatric Disorders: A Single-Center Retrospective
Study. Medicina. 2022;58:1277. doi: 10.3390/medicina58091277. [PMC free article] [PubMed] [CrossRef] [Google Scholar]370.
Sloane
P.D., Whitson H., Williams S.W. Addressing Hearing and Vision
Impairment in Long-Term Care: An Important and Often-Neglected Care
Priority. J. Am. Med. Dir. Assoc. 2021;22:1151–1155. doi: 10.1016/j.jamda.2021.04.024. [PubMed] [CrossRef] [Google Scholar]371.
Ologunagba
M., Kolawole O., Echerenwa A., Silva B. Development and
characterization of capsaicin creams formulated with Grewia
mucilage-HPMC base. J. Sci. Pract. Pharm. 2023;7:365–375. doi: 10.47227/jsppharm.v7i1.3. [CrossRef] [Google Scholar]372.
Trbojević
Ivić J., Milosavić N., Dimitrijević A., Gavrović Jankulović M.,
Bezbradica D., Kolarski D., Veličković D. Synthesis of medium-chain
length capsinoids from coconut oil catalyzed by Candida rugosa lipases. Food Chem. 2017;218:505–508. doi: 10.1016/j.foodchem.2016.09.049. [PubMed] [CrossRef] [Google Scholar]373.
Tangwatcharin
P., Khopaibool P. Activity of virgin coconut oil, lauric acid or
monolaurin in combination with lactic acid against Staphylococcus aureus. Southeast Asian J. Trop. Med. Public Health. 2012;43:969–985. [PubMed] [Google Scholar]374.
Shilling
M., Matt L., Rubin E., Visitacion M.P., Haller N.A., Grey S.F.,
Woolverton C.J. Antimicrobial effects of virgin coconut oil and its
medium-chain fatty acids on Clostridium difficile. J. Med. Food. 2013;16:1079–1085. doi: 10.1089/jmf.2012.0303. [PubMed] [CrossRef] [Google Scholar]375.
Peedikayil
F.C., Remy V., John S., Chandru T.P., Sreenivasan P., Bijapur G.A.
Comparison of antibacterial efficacy of coconut oil and chlorhexidine on
Streptococcus mutans: An in vivo study. J. Int. Soc. Prev. Community Dent. 2016;6:447–452. doi: 10.4103/2231-0762.192934. [PMC free article] [PubMed] [CrossRef] [Google Scholar]376.
Widianingrum
D.C., Noviandi C.T., Salasia S.I.O. Antibacterial and immunomodulator
activities of virgin coconut oil (VCO) against Staphylococcus aureus. Heliyon. 2019;5:e02612. doi: 10.1016/j.heliyon.2019.e02612. [PMC free article] [PubMed] [CrossRef] [Google Scholar]377.
Hariyadi
D.M., Fitri A., Sudarma S., Purwanti T., Erawati T. Optimization of
microspheres containing virgin coconut oil and hydrolyzed virgin coconut
oil as antimicrobial. J. Adv. Pharm. Technol. Res. 2022;13:238–242. doi: 10.4103/japtr.japtr_99_22. [PMC free article] [PubMed] [CrossRef] [Google Scholar]379.
Lassen
C.L., Meyer K., Bredthauer A., Klier T.W. Facial and Oral
Cross-Contamination of a 3-Year-Old Child with High Concentration
Capsaicin: A Case Report. A A Pract. 2020;14:e01258. doi: 10.1213/XAA.0000000000001258. [PubMed] [CrossRef] [Google Scholar]380.
Yeung M.F., Tang W.Y. Clinicopathological effects of pepper (oleoresin capsicum) spray. Hong Kong Med. J. 2015;21:542–552. doi: 10.12809/hkmj154691. [PubMed] [CrossRef] [Google Scholar]381.
Nirmala Grace A., Pandian K. Antibacterial efficacy of aminoglycosidic antibiotics protected gold nanoparticles—A brief study. Colloids Surf. A Physicochem. Eng. Asp. 2007;297:63–70. doi: 10.1016/j.colsurfa.2006.10.024. [CrossRef] [Google Scholar]382.
Turos
E., Shim J.-Y., Wang Y., Greenhalgh K., Reddy G.S.K., Dickey S., Lim
D.V. Antibiotic-conjugated polyacrylate nanoparticles: New opportunities
for development of anti-MRSA agents. Bioorganic Med. Chem. Lett. 2007;17:53–56. doi: 10.1016/j.bmcl.2006.09.098. [PMC free article] [PubMed] [CrossRef] [Google Scholar]383.
Saha
B., Bhattacharya J., Mukherjee A., Ghosh A., Santra C., Dasgupta A.K.,
Karmakar P. In Vitro Structural and Functional Evaluation of Gold
Nanoparticles Conjugated Antibiotics. Nanoscale Res. Lett. 2007;2:614. doi: 10.1007/s11671-007-9104-2. [CrossRef] [Google Scholar]384.
Galdiero S., Falanga A., Vitiello M., Cantisani M., Marra V., Galdiero M. Silver Nanoparticles as Potential Antiviral Agents. Molecules. 2011;16:8894–8918. doi: 10.3390/molecules16108894. [PMC free article] [PubMed] [CrossRef] [Google Scholar]385.
Milovanovic
M., Arsenijevic A., Milovanovic J., Kanjevac T., Arsenijevic N.
Chapter 14—Nanoparticles in Antiviral Therapy. In: Grumezescu A.M.,
editor. Antimicrobial Nanoarchitectonics. Elsevier; Amsterdam, The Netherlands: 2017. pp. 383–410. [CrossRef] [Google Scholar]386.
Gurunathan
S., Qasim M., Choi Y., Do J.T., Park C., Hong K., Kim J.-H., Song H.
Antiviral Potential of Nanoparticles—Can Nanoparticles Fight against
Coronaviruses? Nanomaterials. 2020;10:1645. doi: 10.3390/nano10091645. [PMC free article] [PubMed] [CrossRef] [Google Scholar]387.
Trombino S., Mellace S., Cassano R. Solid lipid nanoparticles for antifungal drugs delivery for topical applications. Ther. Deliv. 2016;7:639–647. doi: 10.4155/tde-2016-0040. [PubMed] [CrossRef] [Google Scholar]388.
Soliman G.M. Nanoparticles as safe and effective delivery systems of antifungal agents: Achievements and challenges. Int. J. Pharm. 2017;523:15–32. doi: 10.1016/j.ijpharm.2017.03.019. [PubMed] [CrossRef] [Google Scholar]389.
Nami
S., Aghebati-Maleki A., Aghebati-Maleki L. Current applications and
prospects of nanoparticles for antifungal drug delivery. EXCLI J. 2021;20:562. [PMC free article] [PubMed] [Google Scholar]390.
Elmi T., Gholami S., Fakhar M., Azizi F. A review on the use of nanoparticles in the treatment. J. Maz. Univ. Med. Sci. 2013;23:126–133. [Google Scholar]391.
Rahul
S., Chandrashekhar P., Hemant B., Bipinchandra S., Mouray E., Grellier
P., Satish P. In vitro antiparasitic activity of microbial pigments and
their combination with phytosynthesized metal nanoparticles. Parasitol. Int. 2015;64:353–356. doi: 10.1016/j.parint.2015.05.004. [PubMed] [CrossRef] [Google Scholar]392.
Sun Y., Chen D., Pan Y., Qu W., Hao H., Wang X., Liu Z., Xie S. Nanoparticles for antiparasitic drug delivery. Drug Deliv. 2019;26:1206–1221. doi: 10.1080/10717544.2019.1692968. [PMC free article] [PubMed] [CrossRef] [Google Scholar]393.
Date A.A., Joshi M.D., Patravale V.B. Parasitic diseases: Liposomes and polymeric nanoparticles versus lipid nanoparticles. Adv. Drug Deliv. Rev. 2007;59:505–521. doi: 10.1016/j.addr.2007.04.009. [PubMed] [CrossRef] [Google Scholar]394.
Matei
A.-M., Caruntu C., Tampa M., Georgescu S.R., Matei C., Constantin M.M.,
Constantin T.V., Calina D., Ciubotaru D.A., Badarau I.A. Applications
of nanosized-lipid-based drug delivery systems in wound care. Appl. Sci. 2021;11:4915. doi: 10.3390/app11114915. [CrossRef] [Google Scholar]