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Cytotoxicity and anti-Leishmania amazonensis activity of Citrus sinensis leaf extracts

机译:柑橘叶片提取物的细胞毒性和抗亚马逊利什曼原虫活性

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摘要

>Context:Leishmania amazonensis is the main agent of diffuse cutaneous leishmaniasis, a disease characterized by lesional polymorphism and the commitment of skin surface. Previous reports demonstrated that the Citrus genus possess antimicrobial activity.>Objective: This study evaluated the anti-L. amazonensis activity of Citrus sinensis (L.) Osbeck (Rutaceae) extracts.>Materials and methods:Citrus sinensis dried leaves were subjected to maceration with hexane (CH), ethyl acetate (CEA), dichloromethane/ethanol (CD/Et – 1:1) or ethanol/water (CEt/W – 7:3). Leishmania amazonensis promastigotes were treated with C. sinensis extracts (1–525 μg/mL) for 120 h at 27 °C. Ultrastructure alterations of treated parasites were evaluated by transmission electron microscopy. Cytotoxicity of the extracts was assessed on RAW 264.7 and J774.G8 macrophages after 48-h treatment at 37 °C using the tetrazolium assay. In addition, Leishmania-infected macrophages were treated with CH and CD/Et (10–80 μg/mL).>Results: CH, CD/Et and CEA displayed antileishmanial activity with 50% inhibitory activity (IC50) of 25.91 ± 4.87, 54.23 ± 3.78 and 62.74 ± 5.04 μg/mL, respectively. Parasites treated with CD/Et (131.2 μg/mL) presented severe alterations including mitochondrial swelling, lipid body formation and intense cytoplasmic vacuolization. CH and CD/Et demonstrated cytotoxic effects similar to that of amphotericin B in the anti-amastigote assays (SI of 2.16, 1.98 and 1.35, respectively). Triterpene amyrins were the main substances in CH and CD/Et extracts. In addition, 80 μg/mL of CD/Et reduced the number of intracellular amastigotes and the percentage of infected macrophages in 63% and 36%, respectively.>Conclusion: The results presented here highlight C. sinensis as a promising source of antileishmanial agents.
机译:>背景:亚马逊利什曼原虫是弥漫性皮肤利什曼原虫病的主要病因,该病以病灶多态性和皮肤表面定型为特征。以前的报道表明柑橘属具有抗菌活性。>目的:该研究评估了抗L素。 >材料和方法:将柑桔干燥的叶子用己烷(CH),乙酸乙酯(CEA),二氯甲烷/乙醇( CD / Et – 1:1)或乙醇/水(CEt / W – 7:3)。在27℃下,用中华C提取物(1-525μg/ mL)处理了亚马逊利什曼原虫前鞭毛体120μh。通过透射电子显微镜评估处理过的寄生虫的超微结构改变。使用四唑鎓测定法在37°C处理48小时后,在RAW 264.7和J774.G8巨噬细胞上评估提取物的细胞毒性。此外,用CH和CD / Et(10–80μg/ mL)处理感染了利什曼原虫的巨噬细胞。>结果: CH,CD / Et和CEA表现出抗粪便活性,抑制活性为50%(IC50 )分别为25.91±4.87、54.23±3.78和62.74±5.04μg/ mL。 CD / Et(131.2μg/ mL)处理的寄生虫表现出严重的变化,包括线粒体肿胀,脂质体形成和强烈的细胞质空泡化。 CH和CD / Et在抗鞭毛虫测定中显示出与两性霉素B相似的细胞毒性作用(SI分别为2.16、1.98和1.35)。三萜烯粉蛋白是CH和CD / Et提取物中的主要物质。另外,CD / Et的80μg/ mL减少了63%和36%的胞内变形虫的数量和巨噬细胞的感染率。>结论:一种很有前途的防毒剂来源。

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