Prakash Jay, Chouhan Shikha, Yadav Satyndra Kumar, Westfall Susan, Rai Sachchida Nand, Singh Surya Pratap
Department of Biochemistry, Faculty of Science, Banaras Hindu University, Varanasi, 221005, Uttar Pradesh, India,
Neurochem Res. 2014 Dec;39(12):2527-36. doi: 10.1007/s11064-014-1443-7. Epub 2014 Nov 18.
Maneb (MB) and paraquat (PQ) are environmental toxins that have been experimentally used to induce selective damage of dopaminergic neurons leading to the development of Parkinson's disease (PD). Although the mechanism of this selective neuronal toxicity in not fully understood, oxidative stress has been linked to the pathogenesis of PD. The present study investigates the mechanisms of neuroprotection elicited by Withania somnifera (Ws), a herb traditionally recognized by the Indian system of medicine, Ayurveda. An ethanolic root extract of Ws was co-treated with the MB-PQ induced mouse model of PD and was shown to significantly rescue canonical indicators of PD including compromised locomotor activity, reduced dopamine in the substantia nigra and various aspects of oxidative damage. In particular, Ws reduced the expression of iNOS, a measure of oxidative stress. Ws also significantly improved the MB + PQ mediated induction of a pro-apoptotic state by reducing Bax and inducing Bcl-2 protein expression, respectively. Finally, Ws reduced expression of the pro-inflammatory marker of astrocyte activation, GFAP. Altogether, the present study suggests that Ws treatment provides nigrostriatal dopaminergic neuroprotection against MB-PQ induced Parkinsonism by the modulation of oxidative stress and apoptotic machinery possibly accounting for the behavioural effects.
代森锰(MB)和百草枯(PQ)是环境毒素,已被用于实验性诱导多巴胺能神经元的选择性损伤,从而导致帕金森病(PD)的发生。尽管这种选择性神经元毒性的机制尚未完全了解,但氧化应激已与PD的发病机制相关联。本研究调查了印度传统医学阿育吠陀中认可的草药睡茄(Ws)所引发的神经保护机制。将Ws的乙醇根提取物与MB - PQ诱导的PD小鼠模型共同处理,结果显示其能显著挽救PD的典型指标,包括运动活性受损、黑质中多巴胺减少以及氧化损伤的各个方面。特别是,Ws降低了诱导型一氧化氮合酶(iNOS)的表达,这是氧化应激的一个指标。Ws还分别通过降低Bax和诱导Bcl - 2蛋白表达,显著改善了MB + PQ介导的促凋亡状态的诱导。最后,Ws降低了星形胶质细胞活化的促炎标志物胶质纤维酸性蛋白(GFAP)的表达。总之,本研究表明,Ws治疗通过调节氧化应激和凋亡机制,为MB - PQ诱导的帕金森症提供黑质纹状体多巴胺能神经保护,这可能解释了其行为学效应。