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Iranian Journal of Parasitology logoLink to Iranian Journal of Parasitology
. 2017 Jul-Sep;12(3):312–322.

Iranian Native Plants on Treatment of Cutaneous Leishmaniosis: A Narrative Review

Elham MOGHADDAS 1, Ali KHAMESIPOUR 2, Mehdi MOHEBALI 3, Abdolmajid FATA 1,4,*
PMCID: PMC5623910  PMID: 28979340

Abstract

Background:

Chemotherapy still relies on the use of pentavalent antimonials, amphotericin B, paromomycin, miltefosin, and allopurinol. In this study, we explained about the native plant that grows in different regions of Iran and used as anti-leishmanial in Iran and even many other countries.

Methods:

This narrative review covers all information about local herbal medicine in Iran that used in treatment of cutaneous leishmaniasis in all the worlds, published in local and international journals from 1996 to 2015 using various databases including PubMed, SID, Google Scholar, Scopus, and Science Direct.

Results:

Overall, 150 articles in databases were identified. Many local plants grown in some places of Iran were used to treat this endemic disease.

Conclusion:

The cutaneous leishmaniasis is also a major health problem in Iran, especially in Mashhad (Northeast of Iran). Therefore, many patients seek for herbal therapy that is cheaper and readily available. This review provides information regarding plant that exists in Iran and exhibiting effects on anti-Leishmania activity. Among the anti-leishmanial mentioned in this review, most have never been tested for cytotoxicity and very few have been tested for in vivo activity.

Keywords: Cutaneous leishmaniasis, Herbal medicine, Treatment, Iran

Introduction

Cutaneous leishmaniasis (CL) is an endemic and sometimes hyperendemic disease in Iran, where it constitutes health problems. About 20000 cases of the disease are reported from different areas of Iran annually (1, 2). During 20 years (1995–2014) 68958 cases of CL were diagnosed only at 5 health centers of Mashhad, the capital city of Khorasan-E-Razavi Province, Northeast Iran (3).

Since 50 years ago pentavalent antimonials are the most common effective medicine used for treatment of CL. Using this group of drugs, sometimes associated with problems such as different responses of patients, drug toxicity, resistance, high failure rate, long course of therapy, and relapse (4). Cardiac and renal insufficiency has been recorded as side effect of these compounds. Despite these flaws, pentavalent antimony is still the first choice of treatment for treatment of different forms of leishmaniasis (5).

In the early 1980s, some reports about untreated patients with these drugs were announced, but unfortunately, there is still no development in the production of novel antileishmanial drug (6). All disadvantages led to an interest in the study of traditional remedies as a source for the development of new chemotherapeutic medicine with better efficiency and less toxicity and side effect. Antiprotozoal herbal drugs are potential sources of alkaloids, alavonoids, phenylpropanoid, steroids, and terpenoids (1, 2). Several plants have been used for the treatment of parasitic disease (Table 1).

Table 1:

Summary of Iranian local plant that used for the treatment of cutaneous leishmaniasis in the world

Plant species Family Extracts or compounds Cultured place Ref
Achillea millefolium Asteraceae Essential oil All of Iran (12, 16)
Tanacetum parthenium Asteraceae Plant powder Kohgiluyeh and Boyer-Ahmad Province (18)
Hydroalcoholic extract (19)
Dichloromethane extract (20)
Carica papaya Caricaceae Tyrosyl esters Sistan baluchestan (21)
Ethanolic extract (22)
Ginkgo biloba Ginkgoaceae Isoginkgetin North of Iran (25)
Quercetin (58)
Nigella sativa Ranunculaceae Thymoquinone Centre of Iran (28)
Alcoholic extract (29)
Berberis vulgaris Berberidaceae Alcoholic extract South Khorasan (33)
Berberine (32)
Plantago psyllium Plantaginaceae Powder North of Iran (36)
Alo vera Xanthorrhoeaceae Leaf exudate South Iran (37)
Aloe-emodin ointment (39)
Plantago major Plantaginaceae Leaves extract Kurdistan province (40, 41)
Dried powder and boiled leaves (59)
Allium sativum Amaryllidaceae Alcoholic extract All of Iran (43, 44, 48)
Allicin (4547)
Green tea Theaceae Ethanolic extract Northern Iran (50)
Dietary polyphenol (flavanol) (51)
Thymus vulgarish Lamiaceae Hydroalcoholic extracts Mountains of Iran (52)
Essential oil (53)
Hexane extract (54)
Salvia officinalis Lamiaceae Methanolic extracts Northern Iran (55, 56)
Artemisia sieberi Asteraceae Alcoholic Essence Desert areas of Kashan (61)
Aqueous extract (63)
Lawsonia inermis Lythraceae Hydroalcoholic extracts South of Iran (66, 67)
Cassia fistula Fabaceae Fruits extracts Northern Iran (53, 55, 56)
Boiled extract Hydroalcoholic extract
Seidlitzia Rosmarinus Chenpodiaceae Hydroalcoholic extract Desert areas of Iran (57, 58)
Euphorbia myrsinitis Euphorbiaceae Soxhlet extracts Sistan baluchestan (5969)
Satureja khuzestanica Lamiaceae Ethanolic and methanolic leaf extracts Khuzestan and Lorestan provinces (7074)

The present study reviewed native Iranian herbal medicine for treatment of CL.

Methods

This narrative review covers all information about local herbal medicine in Iran that used in treatment of CL, published in local and international journals from 1996 to 2015 using various databases including PubMed, SID, Google Scholar, Scopus, and Science Direct.

Results

Achillea millefolium (Common name: yarrow; Persian name: bumadaran)

A. millefolium is a flowering plant in the family Asteraceae grown in northern hemisphere in Europe, Asia and North America (7). Nineteen species of A. millefolium have been recorded from Iran. The juice and extract of this plant have been used as anti-inflammatory, antioxidant, antispasmodic, stomachic and antiseptic drug (8). The gel form is also used as a wound healing in traditional medicine (9). Recently, essential oil extracted from the leaves and flowers of A. millefolium has been studied against Leishmania promastigotes (10, 11). Oil extract of A. millefolium make morphological changes and size of this parasite. Other changes appeared on flagella and cell membrane structures that may lead to rupture of the plasma membrane, formation atypical vacuoles and myelin-like figures in promastigotes (10).

Tanacetum parthenium (Common name: feverfew; Persian name: babouneh)

T. parthenium grows in all regions of Iran with different climates. The roots and rhizomes of this plant have been used in Iranian traditional medicine under the name of Aqhovan. The plant contains numerous pharmacological compounds but the active ingredients are present e.g. Sesquiterpene lactones and parthenolide. Flavonoid glycosides and pinenes are the other active ingredients of Aqhovan. Anticancer, anti-inflammatory, cardiotonic, antispasmodic, emmenagogue, and as an enema for worms are some pharmacologic charactristics. (12). Powder form inhibited the growth of Leishmania spp. (13, 14). “In vitro and in vivo antileishmanial activity of sesquiterpene lactone-rich dichloromethane fraction obtained from Tanacetum parthenium” (15).

Carica papaya (Common name: pawpaw; Persian name: kharboze- derakhti)

C. papaya brought to south of Iran in the 1990s from American countries. It is a famous fruit in tropical region of Iran and is cultivated is widely increasing in these areas. Ascorbic acid, α-tocopherol, beta-carotene, vitamin B1, flavonoids, and niacin are natural important constituent of papaya (16). Tyrosyl lipophilic and ethanoic extract have been reported as leishmanicidal materials on L. major and L. infantum promastigotes (17). It is also known as accessible, nontoxic used prophylactic and cost effectiveness drug for leishmaniasis treatment (18).

Ginkgo biloba (Common name: maidenhair tree; Persian name: ginko)

In traditional Chinese medicines, everyone knows Ginkgo. Recently it is cultivated in Iran. Arediterpene lactones and flavonoides are main components of this plant (19). Approximately 300 different forms were extracted from the leaves ranging 22% and 27% of flavonoid glycosides (20). Isoginkgetin and ginkgetin from G. biloba leaves have anti-Leishmania properties (21). One importance flavonoids in this plant is Quercetin, can be absorbed by humans. Quercetin caused mitochondrial dysfunction and parasite death of L. amazonensis promastigote in vitro (22).

Nigella sativa (Common name: Black Cumin, Black Caraway, Black Onion Seeds, Black Sesame Seeds, Musta Siemen, Grani Neri, Hei Zhong; Persian name: siah daneh)

N. sativa is a common plant traditionally used in the Iranian pickles, bread and foods. The Nigella sativa is used as diuretic, carminative, vermifuge and lactagogue (23). Essential oil, methanolic extract, and thymoquinone of N. sativa were studied on murine macrophages infected with leishman bodies. Thymoquinone showed higher anti-Leishmania effect than other extracts (24). In another study, honey based extract of N. sativa with glucantime is more effective than glucantime alone in scar size and reduce dose of glucantime (P=0.002) (25).

Berberis vulgaris (Common name: Barberry, European Barberry; Persian name: zereshk)

B. vulgaris is cultured in Europe and Asia since ancient time. It is well known in Iran and some other countries in the world. Leaf, root, bark, and fruit have been used for gastrointestinal, cardiovascular, respiratory, skin, renal and infectious diseases. For many years, Iranian people used barberry juice to prevent and treat of fatty liver and high blood pressure (26). Palmatine and particularly berberine are the main important components of this plant (27). Berberin was effective on L. tropica and L. infantum, in vitro. In one study, alcoholic extract of stems, leaves, and root bark has been used for treatment experimental leishmaniasis inoculated by L. major in murine model, successfully (28, 29).

Aloe vera (Common name: aloe; Persian name: Sabrezard)

A. vera grows in southern part of Iran (Boushehr). Remedy of bowel diseases, itching, diabetes, stomach ulcers, asthma, depression, and constipation were reported from Aloe gel (30). A. vera leaf exudate has antileishmanial effect on L. braziliensis, L. mexicana, L. tropica, L. major and L. infantum promastigotes and L. donovani amastigotes (31). Fraction of A. vera, Coriandrum sativum and Ricinus communis on promastigotes and amastigotes of L. infantum were used. A. vera did not differ from pentamidine (P> 0.05) but R. communis and C. sativum were more effective than A. vera on amastigotes in cell culture (32). Growth of L. major amastigotes in vivo and promastigotes in vitro were inhibited by Aloeemodin ointment (1, 8-dihydroxy-3-hydroxymethyl-anthraquinone) (33).

Plantago major (Common name: Birdseed, Broadleaf Plantain, Healing Blade, Hen-plant, White ManÕs Foot; Persian name: barhang)

Plantago spp. is useful to treatment of disorders such as respiratory, wound healing, digestive organs, inflammation, reproductive system, cancer, and blood circulation (34). The genus Plantago comprises 16 species in Iran. Powder dried leaves with honey were used orally before breakfast to healing of ulcers and to treat L. braziliensis skin ulceration (35). In rural area of Brazil, bathing with boiled leaf extract and dried leaf powder is common to treatment cutaneous leishmaniasis due to L. braziliensis (36).

Allium sativum (Common name: garlic; Persian name: sir)

A. sativum (garlic) is a traditional plant has been used as food flavour and herbal medicine for thousands of years in many countries. Different forms of extract have therapeutic effects on many different types of tumours, microbial disease, blood glucose concentration and cardiovascular disorders (37). In one study, BALB/c mice macrophages infected by L. major were treated by garlic extracts (38). In similar study, promastigote growth was controlled by allicin, an active ingredient in A. sativum (39). In another study, cell death of promastigotes occurred after exposed to A. sativum extract (40).

Camellia sinensis (common name: green tea; Persian name: Chay Sabz)

Ethanolic extract of Green tea has higher anti-leishmania effect on promastigotes of L. major in comparison with glucantime (41). The active ingredient is Epigallocatechin-3-gallate (EGCG), a dietary polyphenol (flavanol). EGCG causes mitochondrial damage in L. donovani, L. amazonensis, Trypanosoma rhodesiense, T. brucei and T. cruzi (42).

Thymus vulgaris (Common name: thyme, serpyllum: Persian name: avishan)

T. vulgaris was effective on parasitic disease such as trichomoniasis, amoebiasis, leishmaniasis, giardiasis, and toxoplasmosis (43). Fourteen species of avishan exist in Iran. Steam and fresh flower extract are used in herbal therapy. Comparison to glucantime, hydroalcoholic extract of Achillea millefolium is significantly more effective to reduce of leishmaniasis ulcer size (43). Apoptosis of L. major occurs after adding essential oil and hexane extract of T. vulgaris to cell culture (44, 45). Carvacrol, borneol, thymol are important bioactive components reported as anti-amoebic ingredient (45).

Salvia officinalis (Common name: sage; Persian name: Maryam goli)

There are more than 750 salvias throughout the world. Fifty-eight species of S. officinalis are found in Iran, 17 of which are native varieties. Methanolic extracts of S. officinalis leaves reduces number of amastigote and promastigote of L. major inside the macrophages (46, 47). In addition, tannins and phenols extracted from S. officinalis were effective on L. donovani and L. major (48).

Artemisia sieberi (Common name: wormwood; Persian name: dermane)

A. sieberi is grown at desert areas of Kashan province and many region of Iran. Artemisinin is an aromatic herb found in the extract of some medicinal plants such as A. sieberi (49). It is reported as antimalarial (P. falciparum and P. vivax) and anti-trichinellosis by artemisinin (50). L. major promastigote and amastigotes are very sensitive to aqueous extract of A. sieberi and this component decrease the number of amastigotes in macrophage cell cultures (51).

Lawsonia inermis (Common name: henna, Mehendi; Persian name: hana)

Henna leaves, flowers, seeds, stems bark and roots are used in traditional medicine L. inermis is known as antiparasite and antifungal herb. It is used in infections caused by Trypanosoma, Leishmania, and Plasmodium species (52). Growth of L. major promastigotes is stopped by henna. However, S. officinalis has shown more leishmanicidal activity than L. inermis (53).

Cassia fistula (Common name: golden shower tree; Persian name: khyar chambar, kharnoub)

C. fistula fruit extract is known a famous antibacterial and anti-parasitic herbal medicine (54, 55). Chauhan et al. reported C. fistula hexane extract has significant effect on L. chagasi promastigotes (56). This extract is used in the lesions of CL. It is more effective than hydroalcoholic extract of C. fistula (57). The efficacy of concentrated boiled extract and hydroalcoholic extract of C. fistula is the same. This plant can be used topically with Glucantime to lower drug dose and duration of treatment (58, 59). Studies on side effects and toxicity of this plant showed no adverse reaction after using C. fistula fruit extract even with higher dosages (60). Additive effect of C. fistula fruit extract with glucantime has been considered by several investigators (59, 60).

Seidlitzia rosmarinus (Common name: Julman, Salsola rosmarinus, shenan, Suaeda rosmarinus; Persian name: Eshnan)

S. rosmarinus grows on the salt desert areas of the world. It is cylindrical and has fleshy leaves containing abundant minerals. It is used as forage for animals in desert areas. Leaves and stems are used in soap industry (61). This plant is natives in Khorasan Province and is used for treatment of CL lesions by native. They put pure dried leaves’ powder of S. rosmarinus on their skin lesions suspected to oriental sore. Hydro-alcoholic extract of S. rosmarinus was used with concentrations 5%, 10%, and 15% to treat experimental CL in BALB/c. Survival rate was significantly higher compared to control group (P=0.001) and concentrations below 15% did not show a therapeutic effect on experimental CL ulcers of BALB/c mice (62).

Euphorbia myrsinitis (Common name: spurge; Persian name: Farfion)

Euphorbia grows all over the world. There are seventy species of herbaceous in this genus. The milky latex or sap has medical value with highly toxicity and irritation of skin and eye (63). Main active ingredients are diterpene polyesters and other terpene used as herbal medicine (64). Euphorbia species have been the source of a large number of biologically active compounds (65). Cytotoxicity effect (66), skin irritant (67, 68), dermatitis, conjunctivitis (69) and inflammatory reactions are biological activities of some Euphorbia species (70). Other effects are antioxidant, antiviral (71) and antileishmanial (72, 73). Antileishmaniacidal effect of methanol extracts of Euphorbia lagascae seeds has been studied on L. donovani, L. infantum promastigotes and on L. major and L. donovani amatigotes (73).

Satureja khuzestanica (Persian name: Marzeh khuzestani)

Sixteen species of this genus have been reported from Iran (74). It is well-known for its therapeutic effects and used as antiseptic and analgesic herb. Because Satureja can give a large amount of essential oil, it is used in the pharmaceutical, perfumery, food and cosmetics industries (75). Satureja species have been used in traditional medicine as antibacterial, spasmolytic, diuretic agents and cicatrisant. S. khuzestanica leaves extract contain active ingredients, which could be candidate as suitable herbal drug in treatment of experimental cutaneous leishmaniasis in vivo (76) and used as leishmaniacidal agent in vitro (77, 78). Further studies would therefore be needed to see clinical response and associated toxicities in vivo.

Discussion

“Leishmaniasis is a broad-spectrum parasitic disease reported worldwide. Until now no effective vaccine or drug for the inhibition of parasite has been reported and no effective chemicals for eradication of carriers is provided” (79).

Nowadays, efforts are continued to discover an effective route of treatment to cure CL with minimal side effects. Glucantime is used as a standard medicine, but it has many side effects like erythema, edema, local pruritus, urticarial and sometimes local swelling, nausea and vomiting, diffuse erythema and shock (80). There are still many problems in treatment of CL even by standard protocols. Traditional treatment of CL is a common habit of natives in many endemic areas.

This disease is a great health problem in Iran. The prevalence of infection has been reported as 1.8% to 37.9% in different provinces of Iran (81). There exist more than 250000 genera of medical plants in the world. More than 50 genera of them are effective in treatment of CL lesions. Almost 80% reported which working on CL treatment has used only traditional remedies (82). Many of them grow in special climate and different geographical areas of Iran that are unique in the world. The same time, you can ski at the north of Iran, wear spring coat at the center and swim in the Persian Gulf. All these plants grow in such different climate and nature of Iran. On the other hand the growth condition for each plant is unique for example B. vulgaris grows in south Khorasan Province but E. myrsinites in the north as well as in the south of Iran (83), S. rosmarinus grows in desert climates and this type of environment is observed in many provinces of central and south of Iran.

The question why we do not have enough traditional medicine in the pharmacies and market which we have several antileishmanial plants is noticeable. The main reason may be due to imperfect researches. The investigations on medical plants mostly performed by PhD students, therefore these researches were not continued and followed by other investigators.

According to endemicity of cutaneous leishmaniasis in Iran, we propose more clinical researches to determine the effectiveness and safety of native plants and their active ingredients, and possible toxic substances can lead to the production of efficient and safe drugs for treatment of CL. Formulation and production of ointments containing herbal extract or essential oil are noninvasive method for treatment of CL. Lack of an efficient vaccine and resistance to drugs administered for the treatment of leishmaniasis is required of preparation of herbal ointment on wound healing and finding an effective way of reducing injection pain and the treatment cost.

Conclusion

Ttraditional treatment of CL by herbal medicine is recommended by many investigators. Efficacy and safety of some of the more promising traditional remedies used by local populations as possible future alternatives to Glucantime.

Acknowledgments

This study was supported by Research Center for Cutaneous Leishmaniasis, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.

Footnotes

Conflict of interest

The authors declare that they have no competing interests.

References

  • 1.Valizadeh M, Dalimi A, Fata A, et al. A study on Leishmania species causing cutaneous leishmaniasis in Mashhad using specific monoclonal antibody. Modarres J Med Sci. 2005; 7(2): 107–13. [Google Scholar]
  • 2.Rezai A, Moghaddas E, Bagherpor MR, et al. Identification of Leishmania Species for Cutaneous leishmaniasis in Gonabad, Bardaskan and Kashmar, Central Khorasan, 2015. Jundishapour J Microbiol. 2017; 10(4): e44469. [Google Scholar]
  • 3.Galavizade S, Fata A, Vakili V, et al. Survey the cutaneous leishmaniasis prevalence in Mashhad during the past twenty years and the effect of environmental risk factors. Med J Mashhad Univ. Med Sc.2016; 58(9): 481–546. [Google Scholar]
  • 4.Balaña-Fouce R, Reguera RM, Cubría JC, et al. The pharmacology of leishmaniasis. Gen Pharmacol. 1998; 30(4):435–43. [DOI] [PubMed] [Google Scholar]
  • 5.Mendonça-Filho RR, Rodrigues IA, Alviano DS, et al. Leishmanicidal activity of polyphenolic-rich extract from husk fiber of Cocos nucifera Linn (Palmae). Res Microbiol. 2004;155(3):136–43. [DOI] [PubMed] [Google Scholar]
  • 6.Salman MT, Khan RA, Shukla I. Antibacterial Activity of Nigella sativa Linn. Seed oil against multi-drug resistant bacteria from clinical isolates. Nat Prod Radiance. 2008; 7(1): 10–14. [Google Scholar]
  • 7.Gualtiero S. Guide to Herbs and Spices. Simon & Schuster; London: 1990. [Google Scholar]
  • 8.Candan F, Unlu M, Tepe B, et al. Akpulat Antioxidant and antimicrobial activity of the essential oil and methanol extracts of Achillea millefolium (Asteraceae). J Ethnopharmacol. 2003; 87(2–3):215–20. [DOI] [PubMed] [Google Scholar]
  • 9.Luize PS, Tiuman TS, Morello LG, et al. Effects of medicinal plant extracts on growth of L. amazonensis and T. cruzi. Rev Bras Cienc Farm. 2005; 41:85–94. [Google Scholar]
  • 10.Santos AO, Santin AC, Yamaguchi MU, et al. Antileishmanial activity of an essential oil from the leaves and flowers of Achillea millefolium. Ann Trop Med Parasitol. 2010; 104(6):475–83. [DOI] [PubMed] [Google Scholar]
  • 11.Santoroa GF, Cardosob MG, Guimaraesb LGL, et al. Trypanosoma cruzi: Activity of essential oils from Achillea millefolium, Syzygium aromaticum and Ocimum basilicum on epimastigotes and trypomastigotes. Exp Parasitol. 2007;116(3): 283–90. [DOI] [PubMed] [Google Scholar]
  • 12.Jackson B, McDonald RL. Magic and Medicine of Plants. Dobelis IN; Pleasantville, NY: 1986. [Google Scholar]
  • 13.Tiuman TS, Ueda-Nakamura T, Garcia Cortez DA, et al. Antileishmanial activity of parthenolide, a sesquiterpene lactone isolated from Tanacetum parthenium. Antimicrob Agents Chemother. 2005;49(1):176–82. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.da Silva BP, Cortez DA, Violin TY, et al. Antileishmanial activity of a guaianolide from Tanacetum parthenium. Parasitol Int. 2010;59(4):643–6. [DOI] [PubMed] [Google Scholar]
  • 15.Rabito MF, Britta EA, Pelegrini BL, et al. In vitro and in vivo antileishmanial activity of sesquiterpene lactone-rich dichloromethane fraction obtained from Tanacetum parthenium. Exp Parasitol. 2014; 143: 18–23. [DOI] [PubMed] [Google Scholar]
  • 16.Ross IA. Medicinal Plants of the World. USA: Carica papaya, 1999.
  • 17.Aissa I, Sghair RM, Bouaziz M, et al. Synthesis of lipophilic tyrosyl esters derivatives and assessment of their antimicrobial and antileishmanial activities. Lipids Health Dis. 2012; 11: 13. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Odonne G, Berger F, Stien D, et al. Treatment of leishmaniasis in the Oyapock basin (French Guiana): a K.A.P. survey and analysis of the evolution of phytotherapy knowledge amongst Way˜api Indians. J Ethnopharmacol. 2011; 137: 1228–1239. [DOI] [PubMed] [Google Scholar]
  • 19.Ding C, Chen E, Lindsay RC. Natural accumulation of terpene trilactones in Ginkgo biloba leaves: variations by gender, age and season. Eur Food Res Technol. 2007; 224:615–621. [Google Scholar]
  • 20.Oshio LT. Effect of Ginkgo biloba extract on sperm quality, serum testosterone concentration and histometric analysis of testes from adult Wistar rats. J Med Plants Res. 2015; 9(5)122–131. [Google Scholar]
  • 21.Weniger B1, Vonthron-Sénécheau C, Kaiser M, et al. Comparative antiplasmodial, leishmanicidal and antitrypanosomal activities of several bioflavonoids. Phytomedicine. 2006;13(3):176–80. [DOI] [PubMed] [Google Scholar]
  • 22.Fonseca-Silva F, Inacio JD, Canto-Cavalheiro MM, et al. Reactive Oxygen Species Production and Mitochondrial Dysfunction Contribute to Quercetin Induced Death in L. amazonensis. PLoS One. 2011;6(2):e14666. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Ali BH, Blunden G. Pharmacological and Toxicological Properties of Nigella sativa. Phytother Res. 2003;17(4):299–305. [DOI] [PubMed] [Google Scholar]
  • 24.Mahmoudvand H, Tavakoli R, Sharififar F, et al. Leishmanicidal and cytotoxic activities of Nigella sativa and its active principle, thymoquinone. Pharm Biol. 2015; 53(7):1052–7. [DOI] [PubMed] [Google Scholar]
  • 25.Nilforoushzadeh MA, Hejazi SH, Zarkoob H, et al. Evaluation of effectiveness of Nigella sativa extracts and topical honey application versus topical honey alone along with intralesional injection of Glucantime in the treatment of acute cutaneous leishmaniasis. J Cosmet Dermatol. 2010; 1(2): 51–59. [Google Scholar]
  • 26.Mahmoudvand H, Sharififar F, Sharifi I, et al. In Vitro Inhibitory Effect of Berberis vulgaris (Berberidaceae) and its Main Component, Berberine against Different Leishmania Species. Iran J Parasitol. 2014;9(1):28–36. [PMC free article] [PubMed] [Google Scholar]
  • 27.Vennerstrom JL, Lovelace JK, Waits VB, et al. Berberine derivatives as anti-leishmanial drugs. Antimicrob Agents Chemother. 1990; 34(5):918–21. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Salehabadi A, Karamian M, Farzad MH, et al. Effect of root bark extract of Berberis vulgaris on L. major on BALB/c mice. Parasitol Res. 2014;113(3):953–7. [DOI] [PubMed] [Google Scholar]
  • 29.Fata A, Rakhshandeh H, Berenji F, et al. Treatment of cutaneous leishmaniasis in murine model by alcoholic extract of Berberis vulgaris. Iran J Parasitol. 2006; 1(1): 39–42. [Google Scholar]
  • 30.Rajeswari R, Umadevi M, Sharmila Rahale C, et al. Aloe Vera: The Miracle Plant Its Medicinal and Traditional Uses in India. J Pharmacogn Phytochem. 2012; 1(4):118–124. [Google Scholar]
  • 31.Dutta A, Bandyopadhyay S, Mandal C, et al. Aloe vera leaf exudate induces a caspase-independent cell death in L. donovani promastigotes. J Med Microbiol. 2007; 56(Pt 5):629–36. [DOI] [PubMed] [Google Scholar]
  • 32.Rondon FC, Bevilaqua CM, Accioly MP, et al. In vitro effect of Aloe vera, Coriandrum sativum and Ricinus communis fractions on L. infantum and on murine monocytic cells. Vet Parasitol. 2011; 178(3–4):235–40. [DOI] [PubMed] [Google Scholar]
  • 33.Dalimi A, Delavari M, Ghaffarifar F, et al. In vitro and in vivo antileishmanial effects of aloe-emodin on L. major. J Tradit Complement Med. 2015;5(2):96–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Chiang LC, Ng LT, Chiang W, et al. Immunomodulatory Activities of Flavonoids, Monoterpenoids, Triterpenoids, Iridoid Glycosides and Phenolic Compounds of Plantago Species. Planta Med. 2003;69(7):600–4. [DOI] [PubMed] [Google Scholar]
  • 35.Samuelsen AB. The traditional uses, chemical constituents and biological activities of P. major. A review. J Ethnopharmacol. 2000;71(1–2):1–21. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.França F, Lago EL, Marsden PD. Plants used in the treatment of leishmanial ulcers due to L. braziliensis in an endemic area of Bahia, Brazil. Rev Soc Bras Med Trop. 1996; 29(3):229–32. [DOI] [PubMed] [Google Scholar]
  • 37.Bayan L, Koulivand PH, Gorji A. Garlic: a review of potential therapeutic effects. Avicenna J Phytomed. 2014; 4(1): 1–14. [PMC free article] [PubMed] [Google Scholar]
  • 38.Wabwoba BW, Anjili CO, Ngeiywa MM, et al. Experimental Chemotherapy with Allium Sativum (Liliaceae) Methanolic Extract in Rodents infected With L. major And L. donovani. J Vector Borne Dis. 2010;47(3):160–7. [PubMed] [Google Scholar]
  • 39.Kinuthia GK. Toxicity and efficacy of aqueous crude extracts from Allium sativum, Callistemon citrinus and Moringa stenopetala against L. major. Kabarak J Res Innov. 2015; 3(1): 9–20. [Google Scholar]
  • 40.Khademvatan S, Gharavi MJ, Akhlaghi L, et al. Induction of Apoptosis by Miltefosine in Iranian Strain of L. infantum Promastigotes. Iran J Parasitol. 2009; 4(2): 23–31. [Google Scholar]
  • 41.Feily A, Saki J, Maraghi S, et al. In vitro activity of green tea extract against L. major promastigotes. Int J Clin Pharmacol Ther. 2012; 50(3):233–6. [DOI] [PubMed] [Google Scholar]
  • 42.dos Reis MB, Manjolin LC, Maquiaveli Cdo C, et al. Inhibition of L. amazonensis and Rat Arginases by Green Tea EGCG, (+)- Catechin and (−)- Epicatechin: A Comparative Structural Analysis of Enzyme-Inhibitor Interactions. PLoS One. 2013; 8(11):e78387. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Nilforoushzadeh MA, Shirani-Bidabadi L, Zolfaghari-Baghbaderani A, et al. Comparison of Thymus vulgaris (Thyme), Achillea millefolium (Yarrow) and propolis hydroalcoholic extracts versus systemic glucantime in the treatment of cutaneous leishmaniasis in balb/c mice. J Vector Borne Dis. 2008; 45(4):301–6. [PubMed] [Google Scholar]
  • 44.Mikus J, Harkenthal M, Steverding D, et al. In vitro Effect of Essential oils and isolated mono- and sesquiterpenes on L. major and T. brucei. Planta Med. 2000; 66(4):366–8. [DOI] [PubMed] [Google Scholar]
  • 45.Perez G, Ramoslopez E, Sanchez-Miranda M, et al. Antiprotozoa activity of some essential oils. J Med Plants Res. 2012; 6(15):2901–2908. [Google Scholar]
  • 46.Nikmehr B, Ghaznavi H, Rahbar A, et al. In vitro anti-leishmanial activity of methanolic extracts of Calendula officinalis flowers, Datura stramonium seeds, and Salvia officinalis leaves. Chin J Nat Med. 2014; 12(6):423–7. [DOI] [PubMed] [Google Scholar]
  • 47.Serakta M, Djerrou Z, Mansour-Djaalab H, et al. Antileishmanial activity of some plants growing in Algeria: Juglans regia, Lawsonia inermis and Salvia officinalis. Afr J Tradit Complement Altern Med. 2013; 10(3):427–30. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 48.Kolodziej H, Kiderlen AF. Antileishmanial activity and immune modulatory effects of tannins and related compounds on Leishmania parasitised RAW 264.7 cells. Phytochemistry. 2005;66(17):2056–71. [DOI] [PubMed] [Google Scholar]
  • 49.Doroodgar A, Arbabi M, Razavi MR, et al. Treatment of Cutaneous Leishmaniasis in Murine Model by Hydro Alcoholic Essence of Artemisia sieberi. Iran J Arthropod-Borne Dis. 2008; 2(2): 42–47. [Google Scholar]
  • 50.Saddi M, Sanna A, Cottiglia F, et al. Antiherpes activity of Artemisia arborescens essential oil and inhibition of lateral diffusion in Vero cells. Ann Clin Microbiol Antimicrob. 2007; 6:10. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51.Esavand Heydari F, Ghaffarifar F, Soflaei S, et al. Comparison Between in Vitro Effects of Aqueous Extract of Artemisia seiberi and Artemisinin on L. major. Jundishapur J Nat Pharm Prod. 2013; 8(2):70–5. [PMC free article] [PubMed] [Google Scholar]
  • 52.Dinesh Babu P, Subhasree RS. Antimicrobial Activities of Lawsonia inermis - A Review. Am J Plant Sci. 2009; 2 (4): 231–232. [Google Scholar]
  • 53.Fatahi Bafghi A, Fallahzadeh H, Mosadegh MH. Effectiveness of Lawsonia inermis Extract on Cutaneous Leishmaniasis Lesion in BALB/c Mice. J of Kerman Med Sci. 2008; 15(4): 329–335. [Google Scholar]
  • 54.Yadava RN, Verma V. A new biologically active flavone glycoside from the seeds of Cassia fistula (Linn.). J Asian Nat Prod Res.2003; 5(1):57–61. [DOI] [PubMed] [Google Scholar]
  • 55.Mohebali M, Chenari A, Nazari MR. Effect of Cassia fistula on leishmania major ulcers in small laboratory with mice. Pajouhandeh Q Res J. 1999; 1:14–9. [Google Scholar]
  • 56.Neelam C, Ranjan B, Komal S, et al. Review on Cassia fistula. Int J Res Ayurveda Pharm. 2011; 12(2):426–30. [Google Scholar]
  • 57.Jaffary F, Nilforoushzadeh MA, Moradi SH, et al. Concentrated Extracts of Cassia fistula Versus Intra lesion injection of Meglumine Antimoniate in Treatment of Acute Cutaneous Leishmaniasis. J Skin Stem Cell. 2014; 1(1): e16631. [Google Scholar]
  • 58.Bhalerao SA, Kelkar TS. Traditional Medicinal Uses, Phytochemical Profile and Pharmacological activities of Cassia fistula Linn. Int J Biol Sci. 2012; 1(5): 79–84. [Google Scholar]
  • 59.Sartorelli P, Andrade SP, Melhem MS, et al. Isolation of antileishmanial sterol from the fruits of Cassia fistula using bioguided fractionation. Phytother Res. 2007; 21(7): 644–7. [DOI] [PubMed] [Google Scholar]
  • 60.Ilavarasan R, Mallika M, Venkataraman S. Anti-inflammatory and antioxidant activities of Cassia fistula Linn bark extracts. Afr J Trad. CAM. 2005; 2(1): 70–85. [Google Scholar]
  • 61.Heidari M, Hosseinabadi R, Anbari K, et al. Seidlitzia rosmarinus for lower urinary tract symptoms associated with benign prostatic hyperplasia: A pilot randomized controlled clinical trial. Complement Ther Med. 2014; 22(4):607–13. [DOI] [PubMed] [Google Scholar]
  • 62.Ahmadi M, Fata A, Khamesipour A, et al. The efficacy of hydro alcoholic extract of Seidlitzia rosmarinus on experimental zoonotic cutaneous leishmaniasis lesions in murine model. Avicenna J Phytomed. 2014; 4(6):385–91. [PMC free article] [PubMed] [Google Scholar]
  • 63.Basak SK, Bakshi PK, Basu S, et al. Keratouveitis caused by Euphorbia plant sap. Indian J Ophthalmol. 2009; 57(4):311–3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 64.Miyata S, Wang LY, Yoshida C, et al. Inhibition of cellular proliferation by diterpenes, topoisomerase II inhibitor. Bioorg Med Chem.2006; 14(6):2048–51. [DOI] [PubMed] [Google Scholar]
  • 65.Barla A, 1, Oztürk M, Kültür S, et al. Screening of antioxidant activity of three Euphorbia species from Turkey. Fitoterapia. 2007; 78(6):423–5. [DOI] [PubMed] [Google Scholar]
  • 66.Mucsi I, Molnár J, Hohmann J, et al. Cytotoxicities and anti-herpes simplex virus activities of diterpenes isolated from Euphorbia species. Planta Med. 2001; 67(7):672–4. [DOI] [PubMed] [Google Scholar]
  • 67.Upadhyay RR, Sater AM, Moinzadeh F, et al. Tumor promoting activity of Euphorbia striatella (Boiss) and skin irritant activity of some Euphorbia species. Neoplasma. 1984; 31(3):347–50. [PubMed] [Google Scholar]
  • 68.Kinghorn AD, Evans FJ. A biological screen of selected species of the genus Euphorbia for skin irritant effects. Planta Med. 1975; 28(4): 326–335. [PubMed] [Google Scholar]
  • 69.Eberle MM, Erb C, Flammer J, et al. [Dermatitis and conjunctivitis after contact with Euphorbia myrsinites (wolf’s milk extract)--a case report]. Klin Monbl Augenheilkd. 1999; 215(3):203–4. [DOI] [PubMed] [Google Scholar]
  • 70.Abo KA. Characterization of ingenol: an inflammatory diterpene from some Nigerian euphorbia and Elaeophorbia species. Afr J Med Med Sci. 1994; 23(2):161–3. [PubMed] [Google Scholar]
  • 71.Behravan J, Ramezani M, Alidoost H, et al. Evaluation of anti-phage cp51 effect of Euphorbia myrsinites extract by a plaque reduction assay. Pharmacologyonline. 2010; 2: 788–797. [Google Scholar]
  • 72.Duarte N, Kayser O, Abreu P, et al. Antileishmanial activity of piceatannol isolated from Euphorbia lagascae seeds. Phytother Res. 2008; 22(4):455–7. [DOI] [PubMed] [Google Scholar]
  • 73.Jaafari M.R, Behravan J, BodaghAbadi A, et al. Evaluation of leishmanicidal effect of Euphorbia myrsinites extract by in vitro antileishmanial assay using promastigote of Leishmania major. Iran J Basic Med Sc. 2006: 8: 295–298. [Google Scholar]
  • 74.Malmir M, Serrano R, Reza Gohari A, et al. Characterization Of Satureja Khuzestanica Leaf As A Herbal Medicine. Microsc Microanal. 2014; 20(5):1425–35. [DOI] [PubMed] [Google Scholar]
  • 75.Babaee Khou L, Mohebali M, Niakan Lahiji MR, et al. The therapeutic effect of Eucalyptus, Myrtus, Ferula, Aretmisia, Allium and Urtica extracts against cutaneous leishmaniasis caused by Leishmanaia major in small white mice (outbred). Hakim. 2007; 10: 21–7. [Google Scholar]
  • 76.Kheirandish F, Delfan B, Farhadi S, et al. The effect of Satureja khuzestanica essential oil on the lesions induced by Leishmania major in BALB/c mice. Afr J Pharm Pharmacol. 2011; 5: 648–53. [Google Scholar]
  • 77.Sadeghi-Nejad B, Saki J, Khademvatan S, et al. In vitro antileishmanial activity of the medicinal plant - Satureja khuzestanica jamzad. J Med Plants Res. 2011; 5(24): 5912–5915. [Google Scholar]
  • 78.Mohammadpour G, Marzony ET, Farahmand M. Evaluation of the anti-Leishmania major activity of Satureja bakhtiarica essential oil in vitro. Nat Prod Commun. 2012:7(1):133–6. [PubMed] [Google Scholar]
  • 79.Hadighi R, Mohebali M, Boucher P, et al. Unresponsiveness to glucantime treatment in Iranian cutaneous leishmaniasis due to drug-resistant Leishmania tropica parasites. PLoS Med. 2006; 3(5):e162. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 80.Beheshti M, Ghotbi Sh, Amirizade S. Therapeutic and Adverse Effects of Glucantime Used for Treatment of Cutaneous Leishmaniasis. Shiraz E-Med J. 2007; 8: 155–161. [Google Scholar]
  • 81.Alavinia S, Arzamani K, Reihani M, et al. Some Epidemiological Aspects of Cutaneous Leishmaniasis in Northern Khorasan Province, Iran. Iran J Arthropod Borne Dis. 2009; 3(2):50–4. [PMC free article] [PubMed] [Google Scholar]
  • 82.Weigel MM, Armijos RX. The traditional and conventional medical treatment of cutaneous leishmaniasis in rural Ecuador. Rev Panam Salud Publica. 2001;10(6):395–404. [DOI] [PubMed] [Google Scholar]
  • 83.Heshmati GA. Vegetation characteristics of four ecological zones of Iran. Intl J Agron Plant Prod. 2007; 1(2): 215–224. [Google Scholar]

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