金糠蛋白体外抗利什曼原虫活性的研究

M. Olya, Mahdi Delavari, M. Arbabi, S. Rasti, Hossein Hooshyar, M. Salimian
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引用次数: 1

摘要

目的:尽管在皮肤利什曼病治疗领域进行了各种研究,但仍然没有完善和安全的药物来确定治疗这种疾病。因此,寻找合适药物的探索仍在继续。先前的研究表明,金糠蛋白具有抗利什曼原虫活性;因此,在本研究中;研究了金糠蛋白对利什曼原虫的防治作用。材料与方法:研究了1、2、4、8 μg/ml四种浓度的金糠磷脂对大蠊的作用。分别培养无纺丝和原纺丝体,计算IC50。研究了金糠蛋白诱导promastigotes细胞凋亡的能力,并研究了金糠蛋白处理后promastigotes DNA的断裂程度。随后,研究了金糠蛋白处理对原毛菌超微结构的影响。根据所得结果计算金糠醇对无尾线虫和原线虫的IC50分别为1.007和2.38 μg/ml。结果:金糠蛋白可诱导大鼠肝细胞凋亡。在浓度为8 μg/ml时,细胞凋亡率最高(%80.1),金烷芬诱导的DNA断裂率也最高。经金糠蛋白处理后,原毛菌的体形和游离鞭毛发生了较大的变化。结论:综上所述,金糠醚具有较强的抗利什曼原虫活性,今后将在此基础上进一步开展相关研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antileishmanial activity of auranofin against Leishmania major in vitro
Aim: Despite the various studies done in the field of cutaneous leishmaniasis treatment, there is still no perfect and safe drug for definite treatment of this disease. Therefore, the quest to find an appropriate drug continues. Previous studies have shown that auranofin has anti-leishmanial activity; therefore, in this study; the effect of auranofin on Leishmania major was studied. Materials and Methods: Effectiveness of four concentrations (1, 2, 4, and 8 μg/ml) of auranofin on L. major was studied. After culturing amastigotes and promastigotes of the parasite, IC50 was calculated. The ability of auranofin to induce apoptosis in promastigotes was evaluated, and the degree of fragmentation of promastigotes DNA after treatment with auranofin was studied. Subsequently, the ultrastructural changes induced by treatment with auranofin in promastigotes were studied. Using the obtained results, IC50 of auranofin against amastigotes and promastigotes was calculated as 1.007 and 2.38 μg/ml, respectively. Findings: Showed that auranofin induce apoptosis in L. major. The highest rate of apoptosis (%80.1) occurred at the concentration of 8 μg/ml and also auranofin-induced fragmentation of DNA. Considerable changes occurred in the shape of body and free flagellum of the L. major promastigotes after treatment with auranofin. Conclusion: Based on the results, it can be concluded that auranofin has a considerable anti-leishmanial activity and additional studies in this field will be based on the results.
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