Cell Biology and Physiology Division, Indian Institute of Chemical Biology, 4, Raja S.C. Mullick Road, Kolkata 700032, India.
Exp Parasitol. 2013 Sep;135(1):126-33. doi: 10.1016/j.exppara.2013.06.006. Epub 2013 Jul 3.
Leishmaniasis threatens more than 350 million people worldwide specially in tropical and subtropical region. Antileishmanial drugs that are currently available have various limitations. The search of new drugs from natural products (plants, animals) possessing antileishmanial activity is ventured throughout the world. The present study deals with the antileishmanial activity of Bungarus caeruleus snake venom (BCV) on in vitro promastigotes and amastigotes of Leishmania donovani parasite and leishmania infected BALB/c mice. The effect of BCV on peritoneal macrophage, release of cytokines from the activated macrophages, production of nitric oxide, reactive oxygen species and cytokines were studied in vivo and in vitro. IC50 value of BCV on L. donovani promastigote was 14.5 μg/ml and intracellular amastigote was 11.2 μg/ml. It activated peritoneal macrophages, significantly increased cytokines and interleukin production. BCV (20 μg/kg and 40 μg/kg body weight of mice) decreased parasite count by 54.9% and 74.2% in spleen and 41.4% and 60.4% in liver of infected BALB/c mice. BCV treatment significantly increased production of TNF-α, IFN-γ, ROS, NO in infected mice. Histological studies showed decreased granuloma formation in treated liver as compared with control. Liver and spleen structure was partially restored due to BCV treatment in infected mice. The present study revealed that BCV possessed antileishmanial activity against L. donovani parasite in vivo and in vitro and this activity was partly mediated through immunomodulatory activity involving macrophages.
利什曼病威胁着全球超过 3.5 亿人,尤其是在热带和亚热带地区。目前可用的抗利什曼病药物存在各种局限性。因此,全世界都在从具有抗利什曼病活性的天然产物(植物、动物)中寻找新药。本研究探讨了蓝蛇蛇毒(BCV)对利什曼原虫体外前鞭毛体和无鞭毛体以及利什曼原虫感染 BALB/c 小鼠的抗利什曼病活性。研究了 BCV 对腹腔巨噬细胞的影响、激活巨噬细胞释放细胞因子、一氧化氮、活性氧和细胞因子的产生。体内和体外研究了 IC50 值对 L. donovani 前鞭毛体为 14.5μg/ml,内鞭毛体为 11.2μg/ml。它激活了腹腔巨噬细胞,显著增加了细胞因子和白细胞介素的产生。BCV(20μg/kg 和 40μg/kg 小鼠体重)可使感染 BALB/c 小鼠脾脏寄生虫数量减少 54.9%和 74.2%,肝脏寄生虫数量减少 41.4%和 60.4%。BCV 治疗可显著增加感染小鼠 TNF-α、IFN-γ、ROS、NO 的产生。组织学研究表明,与对照组相比,治疗后的肝脏肉芽肿形成减少。由于 BCV 治疗,感染小鼠的肝脾结构得到部分恢复。本研究表明,BCV 对体内和体外的 L. donovani 寄生虫具有抗利什曼病活性,这种活性部分是通过涉及巨噬细胞的免疫调节活性介导的。