金丝桃(Hypericum thymbrifolium BOISS.植物提取物对主要利什曼原虫、热带利什曼原虫和婴儿利什曼原虫/多诺万尼菌株的影响及其细胞毒性潜力。

H Ozpinar, G Culha, N Ozpinar, T Kaya, B Kara, H Yucel
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引用次数: 0

摘要

利什曼病在全球范围内造成了严重的发病率和死亡率。在我国,利什曼病的病例数在过去十年中大幅增加。在我们的研究中,我们测试了金丝桃、连翘和刺五加植物提取物对大利什曼原虫、热带利什曼原虫和婴儿利什曼原虫/多诺万尼的作用。用 XTT 法评估了这些提取物在人成纤维细胞系中的细胞毒性。通过对植物提取物进行气相色谱-质谱分析,检测了可能的活性成分。在测试的 7 种菌株中,有 4 种在浓度为 50 µg/mL 或更低时检测到对 Glucantime® 的抗药性。用浓度为 100 µg/mL 或更高浓度的植物提取物处理的利什曼病菌株中未发现活的利什曼寄生虫。在对 WI-38 人成纤维细胞系的研究中,植物提取物的浓度不具有细胞毒性。根据气相色谱-质谱(GC-MS)分析,确定了几种具有生物活性和抗寄生虫作用的活性物质,如噻吩(Thiophene)、锗蒽-D(Germacrene-D)、反式-香叶醇(trans-Geranylgeraniol)、吡啶(Pyridine)和马来酰亚胺(Maleimides)。根据这项研究的结果,相信这些已确定的活性物质在得到体内研究的支持后,将为未来的研究铺平道路,并有可能开发成抗利什曼病药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of Hypericum thymbrifolium BOISS. ET NOE, Hypericum scabrum L. and Eryngium creticum LAM. plant extracts on Leishmania major, Leishmania tropica and Leishmania infantum/donovani strains and their cytotoxic potential.

Leishmaniasis causes significant morbidity and mortality worldwide. In our country, there has been a significant increase in the number of cases of leishmaniasis in the last decade. In our study, the effects of Hypericum thymbrifolium, Hypericum scabrum and Eryngium creticum plant extracts were tested on Leishmania major, Leishmania tropica and Leishmania infantum/donovani, which were clinically resistant by not responding to Glucantime® therapy. Cytotoxicity of these extracts were evaluated by XTT method in the human fibroblast cell line. Possible active ingredients were detected by GC-MS analysis from plant extracts. Glucantime® resistance was detected at concentrations of 50 µg/mL and lower in 4 of the 7 strains tested. No living leishmania parasites were found in leishmania strains treated with plant extracts at concentrations of 100 µg/mL or higher. The concentrations of plant extracts included in the study on the WI-38 human fibroblast cell line were not cytotoxic. According to the GC-MS analysis, several active substances with biological activities and anti-parasitic effects, such as Thiophene, Germacrene-D, trans-Geranylgeraniol, Pyridine, and Maleimides, were identified. Based on the findings of the study, it is believed that these identified active substances when supported by in-vivo studies, will pave the way for future research and have the potential to be developed as anti-leishmania drugs.

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