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Hydrogen-saturated saline mediated neuroprotection through autophagy via PI3K/AKT/mTOR pathway in early and medium stages of rotenone-induced Parkinson's disease rats

机译:通过PI3K / AKT / MTOR途径在Rotenone诱导的帕金森病大鼠的早期和中等阶段通过自噬介导的氢饱和盐水通过自噬介导

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Some cardiovascular symptoms in the early stage of Parkinson's disease (PD) were related to degeneration of the rostral ventrolateral medulla (RVLM) catecholaminergic neurons. To date, little is known about the effects of hydrogen water on early stage of PD. Here, protective actions of hydrogen-saturated saline (HS) on rotenone induced PD rats, as well as its underlying mechanisms were investigated. HS was used to treat PD rats at three general stages; early, medium and late, which were represented by rotenone induced rats for 0, 7 and 14 days. HS treatment significantly alleviated the cardiovascular and motor symptoms in rotenone-induced PD rats, improved the survival number of RVLM catecholaminergic neurons and nigral dopamine neurons only in early and medium stages of PD rats. Decreased levels of reactive oxygen species (ROS) and alpha-synuclein (alpha-Syn), transformation of microtubule associated protein 1 light chain 3 (LC3)-I/II and degradation of sequestosome 1 (p62) were detected, as well as increased expression level of autophagy related protein 5 (ATG5) and B-cell lymphoma-2 interacting protein 1 (Beclin-1) in the RVLM and substantia nigra (SN) after HS treatment in early and medium stages of PD rats. In addition, phosphorylation levels of phosphatidylinositol-3-kinase (PI3K), protein kinase B (Akt) and mammalian rapamycin target protein (mTOR) decreased after HS treatment in early and medium stages of PD rats. The results suggested that HS treatment exerted beneficial effects in early and medium stages before motor impairments emerged but not in the late stage of rotenone-induced PD rats. It exerted neuroprotection with RVLM catecholaminergic neurons and nigral dopamine neurons, mediated in part by decreasing levels of ROS and alpha-Syn through increasing autophagy machinery which were partly via inhibiting PI3K-Akt-mTOR pathway.
机译:帕金森病(PD)早期的一些心血管症状与升延长腹膜外髓系(RVLM)儿茶酚胺能神经元的退化有关。迄今为止,关于氢水对Pd早期阶段的影响很少。这里,研究了氢饱和盐水(HS)对RotenOne诱导的Pd大鼠的保护作用以及其下面机制。 HS用于在三个一般阶段治疗PD大鼠;早期,中期和晚期,由RotenOne诱导大鼠表示为0,7和14天。 HS治疗显着缓解了旋转酮诱导的PD大鼠的心血管和电机症状,仅在PD大鼠的早期和中等阶段改善了RVLM儿茶酚胺能神经元和八峰多巴胺神经元的存活率。反应性氧物质(ROS)和α-突触核蛋白(α-SYN)水平降低,检测微管相关蛋白1的转化,并检测杀甾体组1(p62)的降解,以及增加在Pd大鼠早期和中等阶段的HS治疗后,在Pd大鼠早期和中等阶段的HS治疗后,自噬相关蛋白5(ATG5)和B细胞淋巴瘤-2相互作用蛋白1(BECIN-1)的相互作用蛋白1(BECIN-1)。此外,在Pd大鼠早期和中等阶段的HS治疗后,磷脂酰肌醇-3-激酶(PI3K),蛋白激酶B(AKT)和哺乳动物雷帕霉素靶蛋白(MTOR)的磷酸化水平降低。结果表明,在出现的电机损伤之前,HS治疗在早期和中等阶段的效果施加了有益效果,但不在转胸诱导的PD大鼠的晚期。它施加与RVLM Catecholaminergic神经元和八蝇多巴胺神经元的神经保护,通过增加通过抑制PI3K-AKT-MTOR途径的自噬机械降低ROS和α-SYN水平来介导的。

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