Department of Microbiology, Bose Institute, Calcutta, India.
Int J Antimicrob Agents. 2009 Dec;34(6):596-601. doi: 10.1016/j.ijantimicag.2009.08.007. Epub 2009 Sep 26.
Previous studies have demonstrated that diospyrin (1), a quinonoid plant product, can inhibit the growth of Leishmania donovani parasites. Here, several derivatives of 1 were evaluated by the MTT assay and it was observed that the ethanolamine analogue (10) exhibited maximum cytotoxicity [50% inhibitory concentration (IC(50))=2.9 microM] against L. donovani promastigotes. Subsequently, the mode of cell death in promastigotes was investigated through externalisation of membrane-associated phosphatidylserine, mitochondrial membrane depolarisation, DNA laddering and in situ labelling of DNA fragmentation by terminal deoxyribonucleotidyl transferase-mediated dUTP nick-end labelling (TUNEL) methods. Whilst both 1 and 10 were found to induce apoptosis-like death in promastigotes, the effect of 10 was evidently stronger even at a lower concentration. Hence, the ethanolamine derivative (10) of diospyrin (1) may be a prospective 'lead' for the development of novel cytotoxic agents inducing apoptosis in L. donovani parasites.
先前的研究表明,醌类植物产物地诺帕明(1)能够抑制利什曼原虫的生长。在这里,通过 MTT 测定法评估了 1 的几种衍生物,结果发现乙醇胺类似物(10)对利什曼原虫前鞭毛体表现出最大的细胞毒性[50%抑制浓度(IC50)=2.9μM]。随后,通过膜相关磷脂酰丝氨酸的外化、线粒体膜去极化、DNA 梯状电泳以及末端脱氧核糖核苷酸转移酶介导的 dUTP 缺口末端标记(TUNEL)法原位标记 DNA 片段化的方法,研究了前鞭毛体中的细胞死亡方式。虽然 1 和 10 都被发现能诱导前鞭毛体发生类似凋亡的死亡,但 10 的作用显然更强,即使在较低浓度下也是如此。因此,地诺帕明(1)的乙醇胺衍生物(10)可能是一种有前途的“先导”化合物,可用于开发诱导利什曼原虫凋亡的新型细胞毒性药物。