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TTAS,一种新型芪类衍生物,可诱导利什曼原虫细胞凋亡。

TTAS a new stilbene derivative that induces apoptosis in Leishmania infantum.

机构信息

Department of Health Promotion Sciences, Section of Infectious Diseases, University of Palermo, Via del Vespro 129, 90127 Palermo, Italy.

出版信息

Exp Parasitol. 2013 Jan;133(1):37-43. doi: 10.1016/j.exppara.2012.10.006. Epub 2012 Oct 26.

DOI:10.1016/j.exppara.2012.10.006
PMID:23103597
Abstract

Leishmania parasites are able to undergo apoptosis (programmed cell death), similarly to mammalian cells. Recently it was demonstrated in vitro the anti-leishmanial effect of some natural and synthetic stilbenoids including resveratrol and piceatannol. In this study we evaluated the Leishmanicidal activity of a pool of stilbene derivatives which had previously shown high apoptotic efficacy against neoplastic cells. All the compounds tested were capable to decrease the parasite viability in a dose-dependent manner. Trans-stilbenes proved to be markedly more effective than cis-isomers. This was different from that observed in tumor cells in which cis-stilbenes were more potent cytotoxic agents. Trans-3,4',5-trimethoxy-3'-amino-stilbene (TTAS) was the most active stilbene showing in Leishmania infantum a LD(50) value of 2.6 μg/mL. In contrast TTAS showed a low toxicity when tested on normal hemopoietic cells. This compound induced apoptosis in parasites by disrupting the mitochondrial membrane potential. Moreover it shows the ability to block Leishmania parasites in G(2)-M phase of cell cycle in agreement with the data obtained by affinity chromatography that identify tubulin as the putative target of TTAS. In conclusion, our results indicate that some stilbene derivatives are highly effective as anti-leishmanial agents and TTAS represents a pro-apoptotic agent in Leishmania parasites that merit further in vivo investigation.

摘要

利什曼原虫能够像哺乳动物细胞一样发生细胞凋亡(程序性细胞死亡)。最近,有研究人员在体外证明了一些天然和合成的芪类化合物(包括白藜芦醇和漆黄素)具有抗利什曼原虫的作用。在这项研究中,我们评估了一组芪类衍生物的杀利什曼原虫活性,这些衍生物先前已经显示出对肿瘤细胞具有很高的凋亡效果。所有测试的化合物都能够以剂量依赖的方式降低寄生虫的活力。反式芪类化合物比顺式异构体的效果更为显著。这与在肿瘤细胞中观察到的情况不同,顺式异构体是更有效的细胞毒性物质。反式-3,4',5-三甲氧基-3'-氨基-芪(TTAS)是最有效的芪类化合物,对婴儿利什曼原虫的 LD(50)值为 2.6 μg/mL。相比之下,TTAS 在测试正常造血细胞时显示出较低的毒性。该化合物通过破坏线粒体膜电位诱导寄生虫发生细胞凋亡。此外,它还具有阻止利什曼原虫进入细胞周期 G(2)-M 期的能力,这与亲和层析获得的数据一致,表明微管蛋白是 TTAS 的潜在靶标。总之,我们的研究结果表明,一些芪类衍生物是非常有效的抗利什曼原虫药物,TTAS 是利什曼原虫的促凋亡剂,值得进一步进行体内研究。

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