[A Therapeutic Target for Inhibition of Neurodegeneration: Autophagy].

IF 0.2 4区 医学 Q4 NEUROSCIENCES Zhurnal Vysshei Nervnoi Deyatelnosti Imeni I P Pavlova Pub Date : 2016-09-01
A B Pupyshev, T A Korolenko, M A Tikhonova
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引用次数: 0

Abstract

The role of autophagy in cell survival and suppression of neurodegeneration was considered. We discussed its involvement in Alzheimer's, Parkinson's, and Huntington's diseases connected with accumulation of amy- loid-β, α-synuclein, and huntingtin, respectively. Autophagy is reduced in these diseases and in aging as well to various extent. Elimination of accumulated toxic proteins and structures is performed by autophagy mech- anisms (chaperon-mediated autophagy, macroautophagy, selected autophagy) in an interaction with ubiqui- tin-proteasome system. In many cases activation of mTOR-dependent autophagy and mTOR-independent regulatory pathways lead to the therapeutic effect of inhibition of neurodegeneration in cell cultures and an- imal models. Some autophagy enhancers such as resveratrol, metformin, rilmenidine, lithium, and curcumin are tested now in clinical trials.

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[抑制神经变性的治疗靶点:自噬]。
考虑了自噬在细胞存活和抑制神经退行性变中的作用。我们分别讨论了它在阿尔茨海默病、帕金森病和亨廷顿病中与淀粉样蛋白-β、α-突触核蛋白和亨廷顿蛋白积累有关的作用。自噬在这些疾病和衰老过程中也不同程度地减少。积累的有毒蛋白和结构的消除是通过自噬机制(伴侣蛋白介导的自噬、巨噬、选择性自噬)与泛素-锡-蛋白酶体系统相互作用来完成的。在许多情况下,mtor依赖性自噬和mtor非依赖性调节途径的激活导致细胞培养和动物模型中抑制神经变性的治疗效果。一些自噬增强剂,如白藜芦醇、二甲双胍、利美尼定、锂和姜黄素,目前正在临床试验中进行测试。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.70
自引率
33.30%
发文量
9
审稿时长
6-12 weeks
期刊介绍: Information not localized
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