Nataraj Jagatheesan, Manivasagam Thamilarasan, Justin Thenmozhi Arokiasamy, Essa Musthafa Mohamed
Department of Biochemistry and Biotechnology, Annamalai University, Annamalainagar, Tamilnadu, 608002, India.
Department of Food Science and Nutrition, CAMS, Sultan Qaboos University, Muscat, Oman.
Neurochem Res. 2017 May;42(5):1354-1365. doi: 10.1007/s11064-017-2183-2. Epub 2017 Feb 8.
Regulation of various signalling (Ras-MAPK, PI3K and AKT) pathways by augmented activity of neurotrophic factors (NTFs) could prevent or halt the progress of dopaminergic loss in Parkinson's disease (PD). Various in vitro and in vivo experimental studies indicated anti-parkinsonic potential of asiatic acid (AA), a pentacyclic triterpene obtained from Centella asiatica. So the present study is designed to determine the neurotrophic effect of AA against 1-methyl 4-phenyl 1, 2, 3, 6-tetrahydropyridine hydrochloride/probenecid (MPTP/p) neurotoxicity in mice model of PD. AA treatment for 5 weeks significantly attenuated MPTP/p induced motor abnormalities, dopamine depletion and diminished expressions NTFs and tyrosine kinase receptors (TrKB). We further, revealed that AA treatment significantly inhibited the MPTP/p-induced phosphorylation of MAPK/P38 related proteins such as JNK and ERK. Moreover, AA treatment increased the phosphorylation of PI3K, Akt, GSK-3β and mTOR, suggesting that AA activated PI3K/Akt/mTOR signalling pathway, which might be the cause of neuroprotection offered by AA. The present findings provided more elaborate in vivo evidences to support the neuroprotective effect of AA on dopaminergic neurons of chronic Parkinson's disease mouse model and the potential of AA to be developed as a possible new therapeutic target to treat PD.
神经营养因子(NTFs)活性增强对各种信号通路(Ras-MAPK、PI3K和AKT)的调节作用,可能会预防或阻止帕金森病(PD)中多巴胺能神经元的损失。各种体外和体内实验研究表明,积雪草中的五环三萜积雪草苷(AA)具有抗帕金森病的潜力。因此,本研究旨在确定AA对PD小鼠模型中1-甲基-4-苯基-1,2,3,6-四氢吡啶盐酸盐/丙磺舒(MPTP/p)神经毒性的神经营养作用。AA治疗5周可显著减轻MPTP/p诱导的运动异常、多巴胺耗竭,并减少NTFs和酪氨酸激酶受体(TrKB)的表达。我们进一步发现,AA治疗可显著抑制MPTP/p诱导的MAPK/P38相关蛋白(如JNK和ERK)的磷酸化。此外,AA治疗可增加PI3K、Akt、GSK-3β和mTOR的磷酸化,表明AA激活了PI3K/Akt/mTOR信号通路,这可能是AA提供神经保护作用的原因。本研究结果提供了更详细的体内证据,以支持AA对慢性帕金森病小鼠模型多巴胺能神经元的神经保护作用,以及AA作为治疗PD潜在新治疗靶点的开发潜力。