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神经退行性疾病中的线粒体功能障碍。

Mitochondrial dysfunction in neurodegenerative diseases.

机构信息

Department of Neurology and Neuroscience, Weill Medical College of Cornell University, New York, NY, USA.

出版信息

J Pharmacol Exp Ther. 2012 Sep;342(3):619-30. doi: 10.1124/jpet.112.192138. Epub 2012 Jun 13.

Abstract

Neurodegenerative diseases are a large group of disabling disorders of the nervous system, characterized by the relative selective death of neuronal subtypes. In most cases, there is overwhelming evidence of impaired mitochondrial function as a causative factor in these diseases. More recently, evidence has emerged for impaired mitochondrial dynamics (shape, size, fission-fusion, distribution, movement etc.) in neurodegenerative diseases such as Parkinson's disease, Huntington's disease, amyotrophic lateral sclerosis, and Alzheimer's disease. Here, we provide a concise overview of the major findings in recent years highlighting the importance of healthy mitochondria for a healthy neuron.

摘要

神经退行性疾病是一大类神经系统致残性疾病,其特征是神经元亚型的相对选择性死亡。在大多数情况下,有大量证据表明,线粒体功能受损是这些疾病的一个致病因素。最近的证据表明,在帕金森病、亨廷顿病、肌萎缩侧索硬化症和阿尔茨海默病等神经退行性疾病中,线粒体动力学(形状、大小、分裂-融合、分布、运动等)受损。在这里,我们提供了近年来的主要发现的简明概述,强调了健康线粒体对健康神经元的重要性。

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