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. 2019 May 8;8:e1270. doi: 10.31661/gmj.v8i0.1270

An Evidence-Based Review of Medicinal Plants Used for the Treatment of Vaginitis by Avicenna in "the Canon of Medicine"

Somayyeh Khalilzadeh 1, Tahereh Eftekhar 2, Roja Rahimi 3, Mozhgan Mehriardestani 3, Malihe Tabarrai 1,*
PMCID: PMC8344152  PMID: 34466482

Abstract

Vaginitis is one of the most common gynecological problems in reproductive age. Because of the limitations of the conventional drugs, identification of new pharmacological interventions for this disease seems to be necessary. The purpose of this article is to review the medicinal herbs mentioned for the treatment of vaginitis by the great Iranian scientist, Avicenna, in his book "the Canon of Medicine " to scientifically demonstrate their effects and their potential to be used as complementary therapies. The medicinal plants listed for vaginitis treatment in "the Canon of Medicine " were extracted. The scientific name and English common name of the given medicinal plants were searched in databases including PubMed, Scopus, and Cochrane Library until December 2017 to obtain any in vitro, animal, and clinical evidence related to vaginitis. Various pharmacological activities, including anti-inflammatory, wound healing, antimicrobial, antifungal, analgesic, and anti-prostaglandin E2, have been demonstrated for medicinal plants emphasized by Avicenna for vaginitis. Randomized controlled trials (RCTs) on Myrtus reported an improvement in the treatment of bacterial vaginosis. Four RCTs on pomegranate indicated a reduction in inflammatory factors in the patients. Medicinal herbs offered in Herbal Medicine are valuable sources for the treatment of various diseases. Effects and pharmacodynamics having been proved by conventional medicine confirm the effectiveness of these herbs. Therefore, these plants can be used in the treatment of vaginitis thanks to further clinical studies.

Keywords: Vaginitis, Avicenna, Anti-Inflammatory, Antibacterial, Persian Medicine

Introduction

As one of the most common clinical problems, vaginitis causes the referral of 28% of women to gynecology clinic [1]. Vaginitis is associated with a high risk of complications, such as preterm labor, urinary tract infections, and pelvic inflammatory disease, as well as infections affecting the uterus and tubes in the embryo transfer and causing infertility. According to the estimates, vaginitis affects 13 million women every year in the United States [2, 3]. Bacterial vaginosis and vulvovaginal candidiasis are the most common forms of vaginal infection in women, and azoles are usually used to treat them; however, only fluconazole has been approved by the Food and Drug Administration (FDA). These treatments fail to reduce the relapse rate of the disease, and their use is difficult due to the systemic and local side effects of azoles and contraindications in the first trimester of pregnancy [4, 5]. Due to these complications and the microbial resistance that is caused daily to these drugs, it is reasonable to propose available and effective drugs. One of the options is the use of traditional drugs that have been popular among people for many years. The great Iranian scientist, Avicenna (AD 980–1037), has named vaginitis as “Sayalan-e-Rahem” in his book “the Canon of Medicine.” The purpose of this article is to review the names of medicinal plants listed in this book to scientifically prove their effects and their potential to be used as complementary therapies [6, 8].

Search Strategies

The names of medicinal plants listed in the book “the Canon of Medicine” for vaginitis were extracted (Table-1). The PubMed, Scopus, and Cochrane Library databases were searched until December 2017. Search terms include “vaginitis,” “vaginosis,” “vaginal discharge,” “antibacterial,” “antifungal,” “inflammation” or “antioxidant” and the name of each plant in the abstract and title. The obtained articles were evaluated for the in vitro, animal, and clinical evidence related to vaginitis. The articles that had an association with vaginitis were included. Only English articles were considered, and duplicate articles were deleted. The articles that were not available as full text, letter to the editor, case reports, and articles that studied several plants were excluded due to interference.

Table1. Medicinal Plants Used for Treatment of Vaginitis Mentioned in “the Canon of Medicine” .

Scientific name(s) Family Common name(s) Name(s) in “Canon of Medicine” book
Anacyclus pyrethrum (L.) Link Asteraceae Pellitory, Spanish chamomile Aagirgarha
Cymbopogon
schoenanthus (L.)
Spreng.
Poaceae Lemongrass Izkhir
Iris germanica L. Iridaceae Iris, flag Irsa
Marrubium vulgare L. Lamiaceae Common horehound or White horehound Faraasiun
Myrtus communis L. Myrtaceae Myrtle Aas
Piper nigrum L. Piperaceae Black pepper Filfil
Punica granatum L. Lythraceae Pomegranate Jolnar
Qerqus infectoria Fagaceae Oak apple or Oak gall afs

Results

In Traditional Persian Medicine, the term “Sayalan-e-Rahem” refers to any pathological vaginal discharge. Today, vaginitis is one of its most obvious examples. The scientific evidence for the efficacy of the plants listed in “the Canon of Medicine” for the treatment of vaginitis including Anacyclus pyrethrum, Cymbopogon species, Iris germanica, Marrubium vulgare, Myrtus communis, Piper species, Punica granatum, and Quercus infectoria has been presented in the articles summarized in Tables 2, 3, and 4. Also, we tried to show some possible mechanisms of them to treatment vaginitis (Figure-1).

Table 2. In Vitro Studies on Plants Used for Treatment of Vaginitis Mentioned in ‘‘the Canon of Medicine’’ .

Plant Part/extraction Result Attributable active constituent References
Anacyclus pyrethrum (L.)Link Root/ Methanol (50%) extracts Oxidative DNA damage preventive and antioxidant activity Phenolic compounds and ascorbic acid [9]
Cymbopogon
citratus
Crude extracts Antimicrobial effects(against acne-inducing bacteria) - [14]
Iris germanica L. Rhizomes/methanolic extracts



Aerial parts and rhizomes /ethanolic extracts
Antioxidant activity, alfa –amylase inhibition


Antimicrobial(against Bacillus subtilis ATCC 6633.), antioxidant, antimutagenic activities
Isoflavonoids




Phenolic compounds
[23]




[24]
Marrubium vulgare L. Leaves/methanol and acetone extracts


Leaves/ hydroalcoholic extracts
Antioxidant activity



Antioxidant and wound healing properties
Flavonoids and phenylethanoid derivatives

Flavonoids and phenolic compounds
[31]



[32]
Myrtus communis L. Aerial parts/ aqueous and methanolic extract



Leaves/myrtucommulone -containing extracts of myrtle
Antioxidant and antigenotoxic



Inhibits microsomal prostaglandin PGE2 synthase-1
Myricetin-3-o-galactoside and the myricetin-3o-rhamnoside

Myrtucommulone
[35]




[37]
Piper nigrum L. - Suppresses Pyroptosis and Interleukin-1b Release upon ATP Triggering and Bacterial Infection/inhibited the production of E2 and NO induced by IL-1β Piperine [34, 45]
Punica granatum L. Peels/ Ethyl acetate, acetone, MeOH, and
water extracts
Radical-scavenging effect & anti-bacterial activity Phenolic compounds [54]
Qerqusinfectoria Olive. Barks/ the MeOH,
water extracts



Acorns/ethyl acetate extract
High antioxidant, antiproliferative activities


Moderate anti-inflammatory activities
Phenolic compounds




Oleanolic triterpenes
[61]




[62]

PGE2: Prostaglandin E2, IL-1β: Interlukine-1β, NO: Nitric oxide, MeOH: Methanol

Table 3. In Vivo Studies on Plants Used for Treatment of Vaginitis Mentioned in ‘‘the Canon of Medicine’’ .

Plant Part used/solvent used for extraction Method Animal Result Active constituent References
Anacyclus pyrethrum (L.)Link Root/ Aqueous,
ethanol, Chloroform extracts





Root/aqueous
& methanol extracts
Subplantar edema induced by carrageenan in rats/ ear edema induced by arachidonic acid in mice



Acetic acid-induced writhing, hot plate, formalin
tests, the mechanical allodynia were assessed in CFA-induced paw edema
Mice/rat








Male mice
Anti-inflammatory activity








Anti-inflammatory, antinociceptive, antioxidant effects
_









Alkaloids, Phenols
[11]









[12]
Cymbopogon
schoenanthus (L.)
Spreng.
Essential oils Intraperitoneal
injection of casein in mice
Female mice Suppression of neutrophil
Recruitment(anti-inflammatory
activity)
Citral [18]
Marrubium vulgare L. Methanolic extract Carrageenan-induced paw edema Male Wistar rats Anti-inflammatory and antioxidant effects Phenolic compounds, Flavonoids [33]
Myrtus communis L. Aerial parts/aqueous and ethanolic extracts






Leaves /Ethanol extract
Hotplate
, writing tests, xylene-induced
ear edema, a cotton pellet tes



Acetic acid-induced colonic inflammation
Mice









Rat
Antinociceptive, Anti-inflammatory effects




Alleviate colitis
Tannins, Alkaloids, Flavonoids




Flavonoids, Phenolic compounds
[39]









[40]
Piper nigrum L. Ethanol extracts




-





Ethanol extracts
Ovalbumin (OVA)-induced allergic asthma model


Acetic acid induced ulcerative colitis


Tail immersion method, analgesia-meter, hot plate, writing tests/ carrageenan-induced paw edema
Mice





Mice





Rats
Ameliorated allergic inflammation




Amelioration of ulcerative colitis




Analgesic, Anti-inflammatory activities
-





Piperine





Piperine
[47]





[48]





[46]
Qerqus infectoria Olive. Galls/ Water extract






Galls /Alcoholic extract
Three different doses were administered via enema (for the acute toxicity study)


Carrageenan, histamine, serotonin and prostaglandin
E2 (PGE2) induced pawoedemas
Mice







Male Wistar rats, male Swiss albino mice
Galls is unlikely to have significant toxicity





Anti-inflammatory
activity
-







-
[64]







[68]

PGE2: Prostaglandin E2

Table 4. Clinical Studies on Plants Used for Treatment of Vaginitis Mentioned in ‘‘the Canon of Medicine’’ .

Plant Treatment group Control group Study
design
Number
of patients
Treatment
duration
Result References
Myrtus communis L. Leaves vaginal gel in metronidazole base




Paste containing Myrtle










Fruit
syrup
Vaginal gel of metronidazole






Placebo
paste











Placebo
syrup
Randomized clinical trial






Double-blind,
before–after RCT










Double-blinded RCT
80 women







45 patients












45 patients
5 nights







6 days












3 months
Improve the efficacy of bacterial vaginosis therapy in myrtle group


↓The size of ulcers, Pain severity, The level of erythema,
Exudation, Improving the quality of life in patients who
suffer from RAS



↓ Mean number of vaginal bleeding days
& ↓ use of pads in
Myrtle group
[42]







[43]












[38]
Punica granatum L.Spreng. Mouth rinsing with pomegranate extract(PomElla)



Natural pomegranate juice






Pomegranate extract





Pomegranate juice
Mouth rinsing with placebo (corn muffin
mix)





Placebo drink








Placebo drink






Placebo drink
Randomized, single-blinded
controlled trial





Clinical trial








Double-blind RCT





Double-blind RCT

32 subjects
(16 males, 16 females)






9 male elite weightlifters







48 participants





101 patients
4 weeks








15 days








30 days






1 year
↓Total protein and aspartate
aminotransferase in the treatment group




Accelerates
recovery of muscle damage and soreness
and inflammatory markers


↓Plasma inflammatory and oxidative stress biomarkers


↓Systemic inflammation and oxidative stress
[55]








[56]








[57]






[58]
Qercusinfectoria Olive. Topical ointment of Bensal HP (proprietary oak bark extract, Quercus rubra-3%)
SSC Randomized, blinded
controlled
trial
40 patients 6 weeks ↓The Wound
the diameter of the Bensal HP collective group
[69]



RAS: Recurrent aphthous stomatitis, RCT: Randomized controlled trial, SCC: Silver sulfadiazine cream

figure1.

figure1

Mechanisms involved in the management of vaginitis by medicinal plants

A. pyrethrum (L.) Link

Regarding the in-vitro study of A. pyrethrum (L.) Link, 50% methanol extract of this plant exhibits free radical scavenging; thus, protecting the DNA damage [9]. Moreover, essential oil of its aerial parts is active against Candida albicans and Staphylococcus aureus[10]. The aqueous and alcoholic extracts of this plant significantly reduce the induced inflammation in mice and rats [11]. A. pyrethrum (L.) Link root and apple extracts used orally in mice have anti-inflammatory properties and reduce the sensation of pain [12].

‎Cymbopogon. species

In experimental models, lemongrass polysaccharides regulate the immune system and have anti-tumoral effects [13]. Also, the crude extracts of the plant have antimicrobial activity against Propionibacterium acnes and S. epidermidis (causes of acne) [14]. The volatile oil of this plant produces anti-inflammatory and antifungal activity [15], and its antioxidant properties have been proven by in vitro and animal models [16, 17]. Injection of C. schoenanthus essential oil into the mice after casein-induced inflammation in peritoneum suppresses the accumulation of leukocytes and reduces inflammation [18]. The active parts of this plant in the animal model reduce pain, fever, and inflammatory activity [19, 21]. The methanolic extract of lemongrass in the laboratory model on peripheral blood mononuclear cells can strongly inhibit interleukin-1β [22].

I. germanica L.

The Iris root is an isoflavonoid-rich source with antimicrobial and anti-mutagenic properties. Also, its compounds can inhibit the activity of alpha-amylase, which can inhibit glucose uptake or accelerate the production of glycogen in the liver, thereby reducing the blood sugar levels in diabetics [23, 25]. Anti-inflammatory, antimalarial, and anticancer effects of I. germanica have also been proven. I. germanica fails to inhibit C. albicans, but it is effective in the treatment of bacterial and viral infections [26, 28].

M. vulgare L.

The various antioxidant effects of M. vulgare (white horehound) have been proven in many cell and animal models [29, 32]. A study on the effects of methanolic extract of this plant on human skin fibroblasts indicated the improvement of cell proliferation as one of the phases of wound healing [32]. In the animal model, inter-peritoneal injection of M. vulgare ethanolic extract reduces edema and inflammation [33]. In a laboratory study, white horehound has shown strong antibacterial, antifungal, and anti-tumoral effects [34].

M. communis L.

Active derivatives of M. communisL. including myricetin-3-o-galactoside and myricetin-3-o-rhamnoside have anti-genotoxic properties and are involved in apoptosis [35]. Also, in the various laboratory or human models, it has inhibitory effects on prostaglandin E2, in particular, and anti-inflammatory, cytoprotective, and anti-uterine bleeding effects, in general [36, 38]. In the animal model, the aqueous and alcoholic extracts of M. communis have anti-nociceptive and anti-inflammatory effects [39]. M. communisL. has similar effects to Sulfasalazine in the treatment of the acetic acid-induced inflammatory bowel disease in rats. Also, its volatile oil in immunosuppressive mice has antifungal effects against C. albicans [40, 41]. In random clinical trials, comparing metronidazole vaginal gel with its myrtle-based counterpart showed that the latter improved the treatment of bacterial vaginosis [42]. In the case of human recurrent aphthous stomatitis (RAS), the use of the myrtle has been effective [43].

Piper. species

Piperine is one of the black pepper phytochemicals with anti-inflammatory activity. In the cell and animal models, it inhibits ATP-induced pyroptosis and is expected to be used for the treatment of bacterial infections in the future [44]. Moreover, Piperine can control the inflammatory factors involved in the development of human osteoarthritis [45] and expresses anti-inflammatory and analgesic properties in rats [46]. The black pepper ethanolic extract inhibits mast cell activation in the animal samples and reduces the allergic inflammation as well [47]. It also has anti-metastatic, anti-depressant, hepatoprotective, immune-regulating, anti-thyroid, anti-tumoral, antinociceptive, and anti-inflammatory properties [48, 51]. Ethanol extract of P. guineense seed has a potent antifungal effect in the experimental model, and its oral intake has not been toxic to mice [52].

P. granatum L.

Pomegranate is an antifungal and antibacterial herb [53, 54]. Administration of the P. granatum mouthwash in comparison with placebo reduces total protein content in the mouth and decreases the activity of aspartate aminotransferase that is involved in gingivitis prevention [55]. However, the use of pomegranate juice compared with placebo has anti-inflammatory effects on athletes and reduces their muscle pain [56]. In obese subjects, the pomegranate extract reduces the inflammatory and oxidative stress [57]. One-year use of the pomegranate extract in hemodialysis patients reduces the risk of inflammation [58]. One study on pomegranate extract mouth rinsing effects on 55 cases of gingival bleeding showed its anti-bleeding activity [59].

Q. infectoria Olive.

In Persian medicine, the extract of Q. infectoria gall has been claimed to eliminate excessive vaginal discharge. Q. brantii has antibacterial activity in the agar disc diffusion against S. aureus species which are resistant to methicillin and cefixime [60]. The hydro-alcoholic extract of oak in the human laryngeal epidermoid carcinoma (Hep-2) cells has strong anti-proliferative effects [61] and reduces the production of interleukins (IL)-6 and IL-8 in the macrophage [62]. Researchers suggest that occupational exposure to wood dust of the oak tree causes inflammatory responses in the body [63]. However, animal studies have not proven the toxicity of Q. brantii but its immunomodulatory effects [64, 65]. Q. infectoria gall has anti-inflammatory and antioxidant effects on the colitis in mice and anti-dermatophytes in an animal model [66-68]. In the topical treatment of diabetic ulcers, the cream made from the oak extract reduces the diameter of the wound more than the Silver sulfadiazine cream; however, it is not statistically significant [69].

Discussion

Due to its complications such as preterm labor, urinary tract infections, and pelvic inflammatory disease, vaginitis highly affects women’s life [2]. Some plants mentioned in this article, such as pomegranate and black pepper, are present in people’s food basket. Various functions of these plants, e.g., anti-inflammatory, wound healing, anti-proliferative, antimicrobial, antifungal, and analgesic, can be used to treat vaginitis and reduce symptoms (Tables-2, 3, and 4). Vaginitis is caused by a bacterium or a fungus that can be suppressed by most of these plants [14, 24, 42, 44, 54]. The main mechanism for causing vaginitis symptoms such as itching, irritation, and stimulation is inflammation by microorganisms. All of the proposed drugs including Q. infectoria Olive, P. nigrum L., A. pyrethrumL., and M. vulgareL. have anti-inflammatory effects in in-vitro and/or in-vivo studies [12, 33, 48, 68]. The prostaglandins also play a role in the development of vaginitis. According to studies, some plants or their phytochemicals showed the effects of PGE2 inhibition [37, 45, 54]. The presence of analgesic agents is required to reduce the clinical symptoms of vaginitis, which was proved in several plants mentioned earlier [12, 39, 43, 46]. The most active ingredients of the proposed herbs are flavonoids, alkaloids, and phenols, among which flavonoids are present at the root of the A. pyrethrum [9], the leaves of the M. vulgare[31], and the aerial parts of M. communis[40]. Pomegranate, myrtle, and oak are plants investigated in many clinical studies, and their efficacy was proved as well. In different RCTs performed on M. communis, there is an improvement in the treatment of bacterial vaginosis and remission of stomatitis, as well as the reduction of menstrual bleeding [38, 42, 43]. In four RCTs, there is a reduction in inflammatory factors due to the pomegranate use [55-58]. In 40 diabetic patients with Wagner grade-1 or -2 ulcers, the use of topical Q. rubra cream caused a further reduction in ulcer diameter compared with placebo [69].

Conclusion

Medicinal herbs offered in herbal medicine around the world are valuable sources for use in the treatment of various diseases. The great Iranian scientist, Avicenna, in the 11th century mentioned plants for the treatment of vaginitis in his book “the Canon of Medicine.” Accordingly, the present article dealt with the effects and pharmacodynamics of these plants. Based on this study, the usefulness of the plants mentioned for the treatment of vaginitis in “the Canon of Medicine” was confirmed. Therefore, in the future, these plants can be used in the treatment of diseases such as vaginitis with more clinical studies.

Acknowledgment

This study has been partially supported by Tehran University of Medical Sciences (grant No. 96-04-86-37034).

Conflict of Interest

Authors declare no conflict of interest.

References

  • 1.Kent HL. Epidemiology of vaginitis. Am J Obstet Gynecol. 1991;165(4 Pt 2):1168–76. doi: 10.1016/s0002-9378(12)90722-x. [DOI] [PubMed] [Google Scholar]
  • 2.Sianou A, Galyfos G, Moragianni D, Baka S. Prevalence of vaginitis in different age groups among females in Greece. J Obstet Gynaecol. 2017;37(6):790–4. doi: 10.1080/01443615.2017.1308322. [DOI] [PubMed] [Google Scholar]
  • 3.Liu C, Zhang Y, Kong S. Applications and therapeutic actions of complementary and alternative medicine for women with genital infection. Evid Based Complement Alternat Med. 2014;2014:658624. doi: 10.1155/2014/658624. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Boeke AJ, Dekker JH, van Eijk JT, Kostense PJ, Bezemer PD. Effect of lactic acid suppositories compared with oral metronidazole and placebo in bacterial vaginosis: a randomised clinical trial. Genitourin Med. 1993;69(5):388–92. doi: 10.1136/sti.69.5.388. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Pendharkar S, Brandsborg E, Hammarstrom L, Marcotte H, Larsson PG. Vaginal colonisation by probiotic lactobacilli and clinical outcome in women conventionally treated for bacterial vaginosis and yeast infection. BMC Infect Dis. 2015;15:255. doi: 10.1186/s12879-015-0971-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Richter SS, Galask RP, Messer SA, Hollis RJ, Diekema DJ, Pfaller MA. Antifungal susceptibilities of Candida species causing vulvovaginitis and epidemiology of recurrent cases. J Clin Microbiol. 2005;43(5):2155–62. doi: 10.1128/JCM.43.5.2155-2162.2005. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Mobli M, Qaraaty M, Amin G, Haririan I, Hajimahmoodi M, Rahimi R. Scientific evaluation of medicinal plants used for the treatment of abnormal uterine bleeding by Avicenna. Arch Gynecol Obstet. 2015;292(1):21–35. doi: 10.1007/s00404-015-3629-x. [DOI] [PubMed] [Google Scholar]
  • 8. Avicenna. Canon (Al-Qanoon fi-ttib). Beirut: Alaalamy Foundation Publications. 2005.
  • 9. Kalim MD, Bhattacharyya D, Banerjee A, Chattopadhyay S. Oxidative DNA damage preventive activity and antioxidant potential of plants used in Unani system of medicine. BMC Complement Altern Med 2010; 10. [DOI] [PMC free article] [PubMed]
  • 10.Selles C, Dib Mel A, Djabou N, Beddou F, Muselli A, Tabti B. et al. Antimicrobial activity and evolution of the composition of essential oil from Algerian Anacyclus pyrethrum L through the vegetative cycle. Nat Prod Res. 2013;27(23):2231–4. doi: 10.1080/14786419.2013.811409. [DOI] [PubMed] [Google Scholar]
  • 11.Rimbau V, Cerdan C, Vila R, Iglesias J. Antiinflammatory activity of some extracts from plants used in the traditional medicine of North-African countries (II) Phytother Res. 1999;13(2):128–32. doi: 10.1002/(SICI)1099-1573(199903)13:2<128::AID-PTR399>3.0.CO;2-7. [DOI] [PubMed] [Google Scholar]
  • 12. Manouze H, Bouchatta O, Gadhi AC, Bennis M, Sokar Z, Ba-M’hamed S. Anti-inflammatory, antinociceptive, and antioxidant activities of methanol and aqueous extracts of Anacyclus pyrethrum roots. Front Pharmacol 2017; 8(SEP). [DOI] [PMC free article] [PubMed]
  • 13.Bao XL, Yuan HH, Wang CZ, Fan W, Lan MB. Polysaccharides from Cymbopogon citratus with antitumor and immunomodulatory activity. Pharm Biol. 2015;53(1):117–24. doi: 10.3109/13880209.2014.911921. [DOI] [PubMed] [Google Scholar]
  • 14.Chomnawang MT, Surassmo S, Nukoolkarn VS, Gritsanapan W. Antimicrobial effects of Thai medicinal plants against acne-inducing bacteria. J Ethnopharmacol. 2005;101(1-3):330–3. doi: 10.1016/j.jep.2005.04.038. [DOI] [PubMed] [Google Scholar]
  • 15.Tiwara S, Passey M, Clegg A, Mgone C, Lupiwa S, Suve N. et al. High prevalence of trichomonal vaginitis and chlamydial cervicitis among a rural population in the highlands of Papua New Guinea. P N G Med J. 1996;39(3):234–8. [PubMed] [Google Scholar]
  • 16.Wang Z, Hwang SH, Guillen Quispe YN, Gonzales Arce PH, Lim SS. Investigation of the antioxidant and aldose reductase inhibitory activities of extracts from Peruvian tea plant infusions. Food Chem. 2017;231:222–30. doi: 10.1016/j.foodchem.2017.03.107. [DOI] [PubMed] [Google Scholar]
  • 17.Boukhatem MN, Ferhat MA, Kameli A, Saidi F, Kebir HT. Lemon grass (Cymbopogon citratus) essential oil as a potent anti-inflammatory and antifungal drugs. Libyan J Med. 2014;9:25431. doi: 10.3402/ljm.v9.25431. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Abe S, Maruyama N, Hayama K, Inouye S, Oshima H, Yamaguchi H. Suppression of neutrophil recruitment in mice by geranium essential oil. Mediators Inflamm. 2004;13(1):21–4. doi: 10.1080/09629350410001664798. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Brito RG, Guimaraes AG, Quintans JS, Santos MR, De Sousa DP, Badaue-Passos D. et al. Citronellol, a monoterpene alcohol, reduces nociceptive and inflammatory activities in rodents. J Nat Med. 2012;66(4):637–44. doi: 10.1007/s11418-012-0632-4. [DOI] [PubMed] [Google Scholar]
  • 20.Gbenou JD, Ahounou JF, Akakpo HB, Laleye A, Yayi E, Gbaguidi F. et al. Phytochemical composition of Cymbopogon citratus and Eucalyptus citriodora essential oils and their anti-inflammatory and analgesic properties on Wistar rats. Mol Biol Rep. 2013;40(2):1127–34. doi: 10.1007/s11033-012-2155-1. [DOI] [PubMed] [Google Scholar]
  • 21.Tarkang PA, Okalebo FA, Siminyu JD, Ngugi WN, Mwaura AM, Mugweru J. et al. Pharmacological evidence for the folk use of Nefang: antipyretic, anti-inflammatory and antinociceptive activities of its constituent plants. BMC Complement Altern Med. 2015;15:174. doi: 10.1186/s12906-015-0703-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Salim E, Kumolosasi E, Jantan I. Inhibitory effect of selected medicinal plants on the release of pro-inflammatory cytokines in lipopolysaccharide-stimulated human peripheral blood mononuclear cells. J Nat Med. 2014;68(3):647–53. doi: 10.1007/s11418-014-0841-0. [DOI] [PubMed] [Google Scholar]
  • 23.Ibrahim SR, Mohamed GA, Zayed MF, Ross SA. 8-Hydroxyirilone 5-methyl ether and 8-hydroxyirilone, new antioxidant and alpha-amylase inhibitors isoflavonoids from Iris germanica rhizomes. Bioorg Chem. 2017;70:192–8. doi: 10.1016/j.bioorg.2016.12.010. [DOI] [PubMed] [Google Scholar]
  • 24.Burcu B, Aysel U, Nurdan S. Antimicrobial, antioxidant, antimutagenic activities, and phenolic compounds of iris germanica. Ind Crops Prod. 2014;61:526–30. [Google Scholar]
  • 25.Nadaroǧlu H, Demir Y, Demir N. Antioxidant and radical scavenging properties of Iris germanica. Pharm Chem J. 2007;41(8):409–15. [Google Scholar]
  • 26.Sala E, Guasch L, Iwaszkiewicz J, Mulero M, Salvado MJ, Blade C. et al. Identification of human IKK-2 inhibitors of natural origin (Part II): in Silico prediction of IKK-2 inhibitors in natural extracts with known anti-inflammatory activity. Eur J Med Chem. 2011;46(12):6098–103. doi: 10.1016/j.ejmech.2011.09.022. [DOI] [PubMed] [Google Scholar]
  • 27.Asghar SF, Habib ur R, Choudahry MI, Atta ur R. Gas chromatography-mass spectrometry (GC-MS) analysis of petroleum ether extract (oil) and bio-assays of crude extract of Iris germanica. Int J Genet Mol Biol. 2011;3(7):95–100. [Google Scholar]
  • 28.Benoit-Vical F, Imbert C, Bonfils JP, Sauvaire Y. Antiplasmodial and antifungal activities of iridal, a plant triterpenoid. Phytochemistry. 2003;62(5):747–51. doi: 10.1016/s0031-9422(02)00625-8. [DOI] [PubMed] [Google Scholar]
  • 29.Brahmi N, Scognamiglio M, Pacifico S, Mekhoukhe A, Madani K, Fiorentino A. et al. 1H NMR based metabolic profiling of eleven Algerian aromatic plants and evaluation of their antioxidant and cytotoxic properties. Food Res Int. 2015;76(Part 3):334–41. doi: 10.1016/j.foodres.2015.07.005. [DOI] [PubMed] [Google Scholar]
  • 30.Pukalskas A, Venskutonis PR, Salido S, Waard Pd, van Beek TA. Isolation, identification and activity of natural antioxidants from horehound (Marrubium vulgare L) cultivated in Lithuania. Food Chem. 2012;130(3):695–701. [Google Scholar]
  • 31.Amessis-Ouchemoukh N, Abu-Reidah IM, Quirantes-Piné R, Madani K, Segura-Carretero A. Phytochemical profiling, in vitro evaluation of total phenolic contents and antioxidant properties of Marrubium vulgare (horehound) leaves of plants growing in Algeria. Ind Crops Prod. 2014;61(Supplement C):120–9. [Google Scholar]
  • 32.Amri B, Martino E. Marrubium vulgare L Leave Extract: Phytochemical Composition, Antioxidant and Wound Healing Properties. Molecules. 2017;22(11) doi: 10.3390/molecules22111851. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Fathiazad F, Rameshrad M, Asghari S, Hamedeyazdan S, Garjani A, Maleki-Dizaji N. Phytochemical screening and anti-inflammatory effect of Marrubium vulgare L Methanol extract on carrageenan-induced paw inflammation in rats. Pharmaceut Sci. 2017;23(1):3–11. [Google Scholar]
  • 34.Zarai Z, Kadri A, Ben Chobba I, Ben Mansour R, Bekir A, Mejdoub H. et al. The in-vitro evaluation of antibacterial, antifungal and cytotoxic properties of Marrubium vulgare L essential oil grown in Tunisia. Lipids Health Dis. 2011;10:161. doi: 10.1186/1476-511X-10-161. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Hayder N, Bouhlel I, Skandrani I, Kadri M, Steiman R, Guiraud P. et al. In vitro antioxidant and antigenotoxic potentials of myricetin-3-o-galactoside and myricetin-3-o-rhamnoside from Myrtus communis: Modulation of expression of genes involved in cell defence system using cDNA microarray. Toxicol Vitro. 2008;22(3):567–81. doi: 10.1016/j.tiv.2007.11.015. [DOI] [PubMed] [Google Scholar]
  • 36.Zaidi SF, Muhammad JS, Shahryar S, Usmanghani K, Gilani AH, Jafri W. et al. Anti-inflammatory and cytoprotective effects of selected Pakistani medicinal plants in Helicobacter pylori-infected gastric epithelial cells. J Ethnopharmacol. 2012;141(1):403–10. doi: 10.1016/j.jep.2012.03.001. [DOI] [PubMed] [Google Scholar]
  • 37.Koeberle A, Pollastro F, Northoff H, Werz O. Myrtucommulone, a natural acylphloroglucinol, inhibits microsomal prostaglandin E2 synthase-1. Br J Pharmacol. 2009;156(6):952–61. doi: 10.1111/j.1476-5381.2009.00070.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Qaraaty M, Kamali SH, Dabaghian FH, Zafarghandi N, Mokaberinejad R, Mobli M. et al. Effect of myrtle fruit syrup on abnormal uterine bleeding: a randomized double-blind, placebo-controlled pilot study. Daru. 2014;22:45. doi: 10.1186/2008-2231-22-45. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Hosseinzadeh H, Khoshdel M, Ghorbani M. Antinociceptive, anti-inflammatory effects and acute toxicity of aqueous and ethanolic extracts of Myrtus communis L Aerial parts in mice. J Acupunct Meridian Stud. 2011;4(4):242–7. doi: 10.1016/j.jams.2011.09.015. [DOI] [PubMed] [Google Scholar]
  • 40.Sen A, Yuksel M, Bulut G, Bitis L, Ercan F, Ozyilmaz-Yay N. et al. Therapeutic Potential of Myrtus communis Subspcommunis Extract Against Acetic ACID-Induced Colonic Inflammation in Rats. J Food Biochem. 2017;41(1):e12297. [Google Scholar]
  • 41.Najib – Zadeh T, Yadegari M, Naghdi Badi H, Salehnia A. Antifungal Efficacy of Myrtus communis Essential Oils on Oral Candidiasis in Immunosupressed Rats. J Med Plants. 2011;2(38):102–16. [Google Scholar]
  • 42.Masoudi M, Rafieian Kopaei M, Miraj S. A comparison of the efficacy of metronidazole vaginal gel and Myrtus (Myrtus communis) extract combination and metronidazole vaginal gel alone in the treatment of recurrent bacterial vaginosis. Avicenna J Phytomed. 2017;7(2):129–36. [PMC free article] [PubMed] [Google Scholar]
  • 43.Babaee N, Mansourian A, Momen-Heravi F, Moghadamnia A, Momen-Beitollahi J. The efficacy of a paste containing Myrtus communis (Myrtle) in the management of recurrent aphthous stomatitis: a randomized controlled trial. Clin Oral Investig. 2010;14(1):65–70. doi: 10.1007/s00784-009-0267-3. [DOI] [PubMed] [Google Scholar]
  • 44.Liang Y-D, Bai W-J, Li C-G, Xu L-H, Wei H-X, Pan H. et al. Piperine Suppresses Pyroptosis and Interleukin-1β Release upon ATP Triggering and Bacterial Infection. Front Pharmacol. 2016;7:390. doi: 10.3389/fphar.2016.00390. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Ying X, Chen X, Cheng S, Shen Y, Peng L, Xu Hz. Piperine inhibits IL-β induced expression of inflammatory mediators in human osteoarthritis chondrocyte. Int Immunopharm. 2013;17(2):293–9. doi: 10.1016/j.intimp.2013.06.025. [DOI] [PubMed] [Google Scholar]
  • 46.Tasleem F, Azhar I, Ali SN, Perveen S, Mahmood ZA. Analgesic and anti-inflammatory activities of Piper nigrum L. Asian Pac J Trop Med. 2014;7(Supplement 1):S461–S8. doi: 10.1016/S1995-7645(14)60275-3. [DOI] [PubMed] [Google Scholar]
  • 47.Bui TT, Piao CH, Song CH, Shin HS, Shon DH, Chai OH. Piper nigrum extract ameliorated allergic inflammation through inhibiting Th2/Th17 responses and mast cells activation. Cell Immunol. 2017;322:64–73. doi: 10.1016/j.cellimm.2017.10.005. [DOI] [PubMed] [Google Scholar]
  • 48.Gupta RA, Motiwala MN, Dumore NG, Danao KR, Ganjare AB. Effect of piperine on inhibition of FFA induced TLR4 mediated inflammation and amelioration of acetic acid induced ulcerative colitis in mice. J Ethnopharmacol. 2015;164(Supplement C):239–46. doi: 10.1016/j.jep.2015.01.039. [DOI] [PubMed] [Google Scholar]
  • 49.Hwang YP, Yun HJ, Kim HG, Han EH, Choi JH, Chung YC. et al. Suppression of phorbol-12-myristate-13-acetate-induced tumor cell invasion by piperine via the inhibition of PKCα/ERK1/2-dependent matrix metalloproteinase-9 expression. Toxicol Lett. 2011;203(1):9–19. doi: 10.1016/j.toxlet.2011.02.013. [DOI] [PubMed] [Google Scholar]
  • 50.Hu D, Wang Y, Chen Z, Ma Z, You Q, Zhang X. et al. The protective effect of piperine on dextran sulfate sodium induced inflammatory bowel disease and its relation with pregnane X receptor activation. J Ethnopharmacol. 2015;169(Supplement C):109–23. doi: 10.1016/j.jep.2015.04.006. [DOI] [PubMed] [Google Scholar]
  • 51.Jeena K, Liju VB, Umadevi NP, Kuttan R. Antioxidant, Anti-inflammatory and Antinociceptive Properties of Black Pepper Essential Oil (Piper nigrum Linn) J Essent Oil-Bear Plants. 2014;17(1):1–12. [Google Scholar]
  • 52.Ngono Ngane A, Biyiti L, Bouchet P, Nkengfack A, Amvam Zollo PH. Antifungal activity of Piper guineense of Cameroon. Fitoterapia. 2003;74(5):464–8. doi: 10.1016/s0367-326x(03)00112-6. [DOI] [PubMed] [Google Scholar]
  • 53.Anibal PC, Peixoto IT, Foglio MA, Hofling JF. Antifungal activity of the ethanolic extracts of Punica granatum L and evaluation of the morphological and structural modifications of its compounds upon the cells of Candida spp. Braz J Microbiol. 2013;44(3):839–48. doi: 10.1590/S1517-83822013005000060. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54.Negi PS, Jayaprakasha GK. Antioxidant and Antibacterial Activities of Punica granatum Peel Extracts. J Food Sci. 2003;68(4):1473–7. [Google Scholar]
  • 55.DiSilvestro RA, DiSilvestro DJ, DiSilvestro DJ. Pomegranate extract mouth rinsing effects on saliva measures relevant to gingivitis risk. Phytother Res. 2009;23(8):1123–7. doi: 10.1002/ptr.2759. [DOI] [PubMed] [Google Scholar]
  • 56.Ammar A, Turki M, Chtourou H, Hammouda O, Trabelsi K, Kallel C. et al. Pomegranate Supplementation Accelerates Recovery of Muscle Damage and Soreness and Inflammatory Markers after a Weightlifting Training Session. PLoS One. 2016;11(10):e0160305. doi: 10.1371/journal.pone.0160305. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 57.Hosseini B, Saedisomeolia A, Wood LG, Yaseri M, Tavasoli S. Effects of pomegranate extract supplementation on inflammation in overweight and obese individuals: A randomized controlled clinical trial. Compl Ther Clin Pract. 2016;22(Supplement C):44–50. doi: 10.1016/j.ctcp.2015.12.003. [DOI] [PubMed] [Google Scholar]
  • 58.Shema-Didi L, Sela S, Ore L, Shapiro G, Geron R, Moshe G. et al. One year of pomegranate juice intake decreases oxidative stress, inflammation, and incidence of infections in hemodialysis patients: a randomized placebo-controlled trial. Free Radic Biol Med. 2012;53(2):297–304. doi: 10.1016/j.freeradbiomed.2012.05.013. [DOI] [PubMed] [Google Scholar]
  • 59.Batista ALA, Diógenes Alves Uchôa Lins R, de Souza Coelho R, do Nascimento Barbosa D, Moura Belém N, Alves Celestino FJ. Clinical efficacy analysis of the mouth rinsing with pomegranate and chamomile plant extracts in the gingival bleeding reduction. Compl Ther Clin Pract. 2014;20(1):93–8. doi: 10.1016/j.ctcp.2013.08.002. [DOI] [PubMed] [Google Scholar]
  • 60.Moghadam MS, Maleki S, Darabpour E, Motamedi H, Seyyed Nejad SM. Antibacterial activity of eight Iranian plant extracts against methicillin and cefixime restistant Staphylococcous aureus strains. Asian Pacific J Trop Med. 2010;3(4):262–5. [Google Scholar]
  • 61.Şöhretoğlu D, Sabuncuoğlu S, Harput ÜŞ. Evaluation of antioxidative, protective effect against H2O2 induced cytotoxicity, and cytotoxic activities of three different Quercus species. Food Chem Toxicol. 2012;50(2):141–6. doi: 10.1016/j.fct.2011.10.061. [DOI] [PubMed] [Google Scholar]
  • 62.Huang J, Wang Y, Li C, Wang X, He X. Anti-Inflammatory Oleanolic Triterpenes from Chinese Acorns. Molecules. 2016;21(5):669. doi: 10.3390/molecules21050669. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 63.Bornholdt J, Saber AT, Sharma AK, Savolainen K, Vogel U, Wallin H. Inflammatory response and genotoxicity of seven wood dusts in the human epithelial cell line A549. Mutat Res. 2007;632(1):78–88. doi: 10.1016/j.mrgentox.2007.04.016. [DOI] [PubMed] [Google Scholar]
  • 64.Iminjan M, Amat N, Li X-H, Upur H, Ahmat D, He B. Investigation into the Toxicity of Traditional Uyghur Medicine Quercus Infectoria Galls Water Extract. PLoS One. 2014;9(3):e90756. doi: 10.1371/journal.pone.0090756. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 65.Maatta J, Haapakoski R, Lehto M, Leino M, Tillander S, Husgafvel-Pursiainen K. et al. Immunomodulatory effects of oak dust exposure in a murine model of allergic asthma. Toxicol Sci. 2007;99(1):260–6. doi: 10.1093/toxsci/kfm145. [DOI] [PubMed] [Google Scholar]
  • 66.Khanavi M, Sabbagh-Bani-Azad M, Abdolghaffari AH, Vazirian M, Isazadeh I, Rezvanfar MA. et al. On the benefit of galls of Quercus brantii Lindlin murine colitis: the role of free gallic acid. Arch Med Sci. 2014;10(6):1225–34. doi: 10.5114/aoms.2014.47831. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 67.Lee CS, Yi EH, Kim H-R, Huh S-R, Sung S-H, Chung M-H. et al. Anti-dermatitis effects of oak wood vinegar on the DNCB-induced contact hypersensitivity via STAT3 suppression. J Ethnopharmacol. 2011;135(3):747–53. doi: 10.1016/j.jep.2011.04.009. [DOI] [PubMed] [Google Scholar]
  • 68.Kaur G, Hamid H, Ali A, Alam MS, Athar M. Antiinflammatory evaluation of alcoholic extract of galls of Quercus infectoria. J Ethnopharmacol. 2004;90(2):285–92. doi: 10.1016/j.jep.2003.10.009. [DOI] [PubMed] [Google Scholar]
  • 69.Jacobs AM, Tomczak R. Evaluation of Bensal HP for the Treatment of Diabetic Foot Ulcers. Adv Skin Wound Care. 2008;21(10):461–5. doi: 10.1097/01.ASW.0000323573.57206.7b. [DOI] [PubMed] [Google Scholar]

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