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慢病毒介导的胱硫醚-β-合酶过表达对6-羟基多巴胺诱导的帕金森病大鼠的神经保护作用

Neuroprotective effects of lentivirus-mediated cystathionine-beta-synthase overexpression against 6-OHDA-induced parkinson's disease rats.

作者信息

Yin Wei-Lan, Yin Wei-Guo, Huang Bai-Sheng, Wu Li-Xiang

机构信息

Department of Physiology, Xiangya School of Medicine, Central South University, Changsha, 410078, Hunan, China; Department of Physiology & Institute of Neuroscience, University of South China, Hengyang 421001, Hunan, China.

The Sixth Affiliated Hospital of Guangzhou Medical University, Qingyuan City People's Hospital, Qingyuan, 511518, Guangdong, China; Department of Clinical Laboratory, Yuebei People's Hospital Affiliated to Medical College of Shantou University, Shaoguan, 512026, Guangdong, China.

出版信息

Neurosci Lett. 2017 Sep 14;657:45-52. doi: 10.1016/j.neulet.2017.07.019. Epub 2017 Jul 29.

Abstract

Parkinson's disease (PD) is age-related neurodegenerative disorder by a progressive loss of dopaminergic(DA) neurons in the substantia nigra (SN) and striatum, which is at least partly associated with α-synuclein protein accumulation in these neurons. Hydrogen sulfide (HS) plays an important role in the nervous system. Studies have shown that HS has a protective effect on PD. However, as a kind of gas molecules, HS is lively, volatile, and not conducive to scientific research and clinical application. Cystathionine-beta-synthase(CBS) is the main enzymes of synthesis of HS in the brain. In order to examine the neuroprotective effects of CBS on PD, we detected the effects of CBS overexpression on 6-Hydroxydopamine (6-OHDA)-lesioned PD rats using lentivirus-mediated gene transfection techniques. In the injured SN of 6-OHDA-induced PD rats, the CBS expression and the endogenous HS level markedly decreased, while administration of lentivirus-mediated CBS overexpression increased the CBS expression and the endogenous HS production.CBS overexpression dramatically reversed apomorphine-induced rotation of the 6-OHDA model rats, decreased the number of TUNEL-positive neurons and the loss of the nigral DA neurons,specifically inhibited 6-OHDA-induced oxidase stress injury, and down-regulated the expression of α-synuclein(α-SYN) in the injured SN. NaHS (an HS donor) had similar effects to CBS overexpression, while Amino-oxyacetate(AOAA, a CBS inhibitor) had opposite effects on PD rats. In summary, we demonstrated that CBS overexpression was able to provide neuroprotective on PD rats and improving the expression of CBS may be a potential therapeutic method for PD.

摘要

帕金森病(PD)是一种与年龄相关的神经退行性疾病,其特征是黑质(SN)和纹状体中多巴胺能(DA)神经元逐渐丧失,这至少部分与这些神经元中α-突触核蛋白的积累有关。硫化氢(HS)在神经系统中起重要作用。研究表明,HS对PD具有保护作用。然而,作为一种气体分子,HS活泼、易挥发,不利于科学研究和临床应用。胱硫醚-β-合酶(CBS)是大脑中合成HS的主要酶。为了研究CBS对PD的神经保护作用,我们使用慢病毒介导的基因转染技术检测了CBS过表达对6-羟基多巴胺(6-OHDA)损伤的PD大鼠的影响。在6-OHDA诱导的PD大鼠受损的SN中,CBS表达和内源性HS水平明显降低,而给予慢病毒介导的CBS过表达则增加了CBS表达和内源性HS的产生。CBS过表达显著逆转了阿扑吗啡诱导的6-OHDA模型大鼠的旋转行为,减少了TUNEL阳性神经元的数量和黑质DA神经元的损失,特异性抑制了6-OHDA诱导的氧化应激损伤,并下调了受损SN中α-突触核蛋白(α-SYN)的表达。硫氢化钠(NaHS,一种HS供体)对PD大鼠的作用与CBS过表达相似,而氨基氧乙酸(AOAA,一种CBS抑制剂)对PD大鼠的作用则相反。总之,我们证明CBS过表达能够对PD大鼠提供神经保护作用,提高CBS的表达可能是PD的一种潜在治疗方法。

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