肌萎缩侧索硬化
疾病
神经科学
亨廷顿病
线粒体
神经退行性变
退行性疾病
线粒体融合
生物
运动障碍
医学
线粒体DNA
中枢神经系统疾病
病理
遗传学
基因
作者
Ashu Johri,M. Flint Beal
标识
DOI:10.1124/jpet.112.192138
摘要
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 Parkinson9s disease, Huntington9s disease, amyotrophic lateral sclerosis, and Alzheimer9s disease. Here, we provide a concise overview of the major findings in recent years highlighting the importance of healthy mitochondria for a healthy neuron.
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