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脑线粒体疾病。

Mitochondrial diseases of the brain.

机构信息

CSIR-Indian Institute of Toxicology Research, 80 MG Marg, Lucknow 226001, India.

出版信息

Free Radic Biol Med. 2013 Oct;63:1-29. doi: 10.1016/j.freeradbiomed.2013.03.018. Epub 2013 Apr 6.

Abstract

Neurodegenerative disorders are debilitating diseases of the brain, characterized by behavioral, motor and cognitive impairments. Ample evidence underpins mitochondrial dysfunction as a central causal factor in the pathogenesis of neurodegenerative disorders including Parkinson's disease, Huntington's disease, Alzheimer's disease, Amyotrophic lateral sclerosis, Friedreich's ataxia and Charcot-Marie-Tooth disease. In this review, we discuss the role of mitochondrial dysfunction such as bioenergetics defects, mitochondrial DNA mutations, gene mutations, altered mitochondrial dynamics (mitochondrial fusion/fission, morphology, size, transport/trafficking, and movement), impaired transcription and the association of mutated proteins with mitochondria in these diseases. We highlight the therapeutic role of mitochondrial bioenergetic agents in toxin and in cellular and genetic animal models of neurodegenerative disorders. We also discuss clinical trials of bioenergetics agents in neurodegenerative disorders. Lastly, we shed light on PGC-1α, TORC-1, AMP kinase, Nrf2-ARE, and Sirtuins as novel therapeutic targets for neurodegenerative disorders.

摘要

神经退行性疾病是大脑的一种使人虚弱的疾病,其特征是行为、运动和认知障碍。大量证据表明,线粒体功能障碍是帕金森病、亨廷顿病、阿尔茨海默病、肌萎缩侧索硬化症、弗里德里希共济失调和腓骨肌萎缩症等神经退行性疾病发病机制中的一个核心因果因素。在这篇综述中,我们讨论了线粒体功能障碍的作用,如生物能量缺陷、线粒体 DNA 突变、基因突变、线粒体动力学改变(线粒体融合/裂变、形态、大小、运输/转运和运动)、转录受损以及突变蛋白与线粒体的关联在这些疾病中的作用。我们强调了线粒体生物能剂在神经退行性疾病的毒素和细胞及遗传动物模型中的治疗作用。我们还讨论了神经退行性疾病中生物能剂的临床试验。最后,我们探讨了过氧化物酶体增殖物激活受体 γ 共激活因子 1α、雷帕霉素靶蛋白复合物 1、腺苷酸活化蛋白激酶、核因子红细胞 2 相关因子 2-抗氧化反应元件和沉默调节蛋白作为神经退行性疾病的新的治疗靶点。

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