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Antifungal Activity of Terminalia avicennioides in Drosophila melanogaster as an Infectious Model

机译:常年碘苯丙烷基毒剂的抗真菌活性作为传染性模型

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Background and Objective: Conventional antifungal agents have become less effective against fungal pathogens especially, Aspergillus fumigatus and Aspergillus flavus because of the toxicity and resistance. This has prompted the search for novel prototype antifungals from higher plants. The present study determined the antifungal activity of leave, stem bark and root extracts of Terminalia avicennioides in vitro and in vivo against Aspergillus fumigatus , Aspergillus flavus and Aspergillus terreus in Drosophila melanogaster . Materials and Methods: In the in vitro and in vivo evaluation of antifungal potentials of the extracts was measured using the microdilution method in a 96-well diffusion method. Survival of Drosophila melanogaster (Drs-LacZ III) challenged with A. fumigatus , A. flavus and A. terreus by ingestion method was used to evaluate in vivo activity. Results: Antifungal activity increased in a concentration dependent manner. There was increased activity with increased concentrations. A. fumigatus , A. flavus and A. terreus was more susceptible to dichloromethane followed by ethyl acetate extract of the leave and roots of T. avicennioide. MIC of 0.32- 0.18 mg mLG1 was recorded against test organisms after 24 and 48 h with Amphotericin B as standard antifungal drug and with the petroleum ether, ethyl acetate, dichloromethane and ethanol leave, stem bark and root extracts. Survival rate increased by more than 50% in flies treated with dichloromethane and ethyl acetate leave and root extract of T. avicennioides. Drosomycin, an AMP increased as fungal infection progressed. Conclusion: The antifungal results in vitro and in vivo validated the use of this plant in traditional medicine in the treatment of fungal infections. These results have stressed the need for isolation and characterization of the active compound and the elucidation of the mechanisms of action of secondary metabolites on the immune response of Drosophila melanogaster.
机译:背景和目的:常规的抗真菌剂对真菌病原体的效果较小,特别是由于毒性和抗性,曲霉属Fumigatus和Aspergillus flavus。这促使从高等植物搜索新型原型抗真菌。本研究确定了在体外和体内毒性和体内的终端炎碘苯二烯苷的抗真菌活性,患有曲霉菌,曲霉和曲霉和曲霉在果蝇的菊毛虫。材料和方法:在体外和体内评估提取物的抗真菌电位,使用微稀释方法在96孔扩散法中测量。用A. fumigatus挑战果蝇(Drs-Lacz III)的生存,A.Fumigatus和A.Terreus用于评估体内活动。结果:抗真菌活性以浓度依赖性方式增加。浓度增加的活性增加。 A. fumigatus,A.FlaVus和A.Terreus更容易对二氯甲烷的影响,然后是乙酸乙酸乙酯提取物的乙酸乙酰苯胺。在24至48小时后用两性蛋白B作为标准抗真菌药物,用石油醚,乙酸乙酯,二氯甲烷和乙醇留下,干树皮和根提取物,记录0.32-0.18mg的MIC。用二氯甲烷和乙酸乙酯的乙酸乙酯和乙酸乙酸乙酸乙酸乙酸乙酯和乙酸乙酸根提取物增加了50%以上的50%以上。德罗丝霉素,AMP随着真菌感染而增加。结论:体外和体内的抗真菌效果验证了这种植物在传统医学中的使用治疗真菌感染。这些结果强调了有必要分离和表征活性化合物和阐释次级代谢产物对果蝇的免疫应答的作用机制。

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