Lemon grass (Cymbopogon citratus) essential oil as a potent anti-inflammatory and antifungal drugs

被引:162
|
作者
Boukhatem, Mohamed Nadjib [1 ]
Ferhat, Mohamed Amine [2 ]
Kameli, Abdelkrim [3 ]
Saidi, Fairouz [1 ]
Kebir, Hadjer Tchoketch [1 ]
机构
[1] Univ Blida 1, Fac Sci Nat & Vie, Dept Biol & Physiol Cellulaire, Blida, Algeria
[2] Ecole Normale Super Kouba, Dept Chim, Lab Rech Prod Bioactifs & Valorisat Biomasse, Algiers, Algeria
[3] Ecole Normale Super Kouba, Dept Nat Sci, Lab Ecophysiol Vegetale, Algiers, Algeria
关键词
lemon grass; essential oil; antifungal activity; anti-inflammatory effect; citral; aromatherapy; ANTIBACTERIAL ACTIVITY; VAPOR-PHASE; CONSTITUENTS; INFLAMMATION; SUPPRESSION; STAPF;
D O I
10.3402/ljm.v9.25431
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Volatile oils obtained from lemon grass [Cymbopogon citratus (DC.) Stapf, Poaceae family] are used in traditional medicine as remedies for the treatment of various diseases. Aims: In the present study, lemon grass essential oil (LGEO) was evaluated for its in vivo topical and oral anti-inflammatory effects, and for its in vitro antifungal activity using both liquid and vapor phases. Methods: The chemical profile of LGEO as determined by gas chromatography-mass spectrometry analysis revealed two major components: geranial (42.2%), and neral (31.5%). The antifungal activity of LGEO was evaluated against several pathogenic yeasts and filamentous fungi using disc diffusion and vapor diffusion methods. Results: LGEO exhibited promising antifungal effect against Candida albicans, C. tropicalis, and Aspergillus niger, with different inhibition zone diameters (IZDs) (35-90 mm). IZD increased with increasing oil volume. Significantly, higher anti-Candida activity was observed in the vapor phase. For the evaluation of the anti-inflammatory effect, LGEO (10 mg/kg, administered orally) significantly reduced carrageenan-induced paw edema with a similar effect to that observed for oral diclofenac (50 mg/kg), which was used as the positive control. Oral administration of LGEO showed dose-dependent anti-inflammatory activity. In addition, topical application of LGEO in vivo resulted in a potent anti-inflammatory effect, as demonstrated by using the mouse model of croton oil-induced ear edema. To our knowledge, this is the first such report to be published. The topical application of LGEO at doses of 5 and 10 mu L/ear significantly reduced acute ear edema induced by croton oil in 62.5 and 75% of the mice, respectively. In addition, histological analysis clearly confirmed that LGEO inhibits the skin inflammatory response in animal models. Conclusion: Results of the present study indicate that LGEO has a noteworthy potential for the development of drugs for the treatment of fungal infections and skin inflammation that should be explored in future studies.
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页数:10
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