Department of Pharmaceutical Technology, Jadavpur University, Kolkata, 700032, India.
Parasitol Res. 2011 Apr;108(4):861-71. doi: 10.1007/s00436-010-2127-0. Epub 2010 Nov 18.
Leishmanial diseases, posing a public health problem worldwide, are caused by Leishmania parasites with a dimorphic life cycle alternating between the promastigote and amastigote forms. Promastigotes transmitted by the vector are transformed into amastigotes residing in the host tissue macrophages. Presently, new antiparasitic agents are needed against Leishmania donovani and Leishmania major, the respective organisms causing visceral and cutaneous leishmaniasis, since the available treatments are unsatisfactory due to toxicity, high cost, and emerging drug resistance. Over the years, traditional medicinal flora throughout the world enriched the modern pharmacopeia. Hence, roots of 'Indian Valerian' (Valeriana wallichii DC) were studied for its antileishmanial activity for the first time. The methanol and chloroform extracts showed activity against L. donovani promastigotes and both promastigotes and amastigotes of L. major. The most active fraction, F3, obtained from the chloroform extract, showed IC(50) at ∼ 3-7 μg/ml against both the promastigotes and 0.3 μg/ml against L. major amastigotes. On investigation of the mechanism of cytotoxicity in L. donovani promastigotes, the 'hall-mark' events of morphological degeneration, DNA fragmentation, externalization of phosphatidyl serine, and mitochondrial membrane depolarization indicated that F3 could induce apoptotic death in leishmanial cells. Therefore, the present study revealed a novel and unconventional property of V. wallichii root as a prospective source of effective antileishmanial agents.
利什曼病是一种全球性的公共卫生问题,由具有二形生命周期的利什曼原虫引起,其生命周期在前鞭毛体和无鞭毛体之间交替。通过媒介传播的前鞭毛体转化为存在于宿主组织巨噬细胞中的无鞭毛体。目前,由于毒性、高成本和耐药性的出现,需要针对利什曼原虫和利什曼原虫的新抗寄生虫药物,因为现有的治疗方法并不令人满意。多年来,世界各地的传统药用植物群丰富了现代药典。因此,首次研究了“印度缬草根”(缬草)的根对利什曼原虫的抗利什曼活性。甲醇和氯仿提取物对利什曼原虫前鞭毛体和利什曼原虫的前鞭毛体和无鞭毛体均具有活性。从氯仿提取物中获得的最活性部分 F3 对两种前鞭毛体的 IC 50 约为 3-7 μg/ml,对利什曼原虫无鞭毛体的 IC 50 为 0.3 μg/ml。在研究 F3 在利什曼原虫前鞭毛体中的细胞毒性机制时,形态退化、DNA 片段化、磷脂酰丝氨酸外化和线粒体膜去极化的“标志”事件表明,F3 可诱导利什曼细胞的凋亡死亡。因此,本研究揭示了缬草根作为有效抗利什曼原虫药物潜在来源的一种新的非常规特性。