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电子传递紊乱与神经退行性变:从阿尔伯特·圣捷尔吉的概念(塞格德)到增强线粒体生物能量学的新方法。

Electron Transport Disturbances and Neurodegeneration: From Albert Szent-Györgyi's Concept (Szeged) till Novel Approaches to Boost Mitochondrial Bioenergetics.

作者信息

Szalárdy Levente, Zádori Dénes, Klivényi Péter, Toldi József, Vécsei László

机构信息

Department of Neurology, Faculty of Medicine, Albert Szent-Györgyi Clinical Center, University of Szeged, Semmelweis u. 6, Szeged 6725, Hungary.

Department of Physiology, Anatomy and Neuroscience, University of Szeged, Közép Fasor 52, Szeged 6726, Hungary ; MTA-SZTE Neuroscience Research Group, Semmelweis u. 6, Szeged 6725, Hungary.

出版信息

Oxid Med Cell Longev. 2015;2015:498401. doi: 10.1155/2015/498401. Epub 2015 Aug 2.

Abstract

Impaired function of certain mitochondrial respiratory complexes has long been linked to the pathogenesis of chronic neurodegenerative disorders such as Parkinson's and Huntington's diseases. Furthermore, genetic alterations of mitochondrial genome or nuclear genes encoding proteins playing essential roles in maintaining proper mitochondrial function can lead to the development of severe systemic diseases associated with neurodegeneration and vacuolar myelinopathy. At present, all of these diseases lack effective disease modifying therapy. Following a brief commemoration of Professor Albert Szent-Györgyi, a Nobel Prize laureate who pioneered in the field of cellular respiration, antioxidant processes, and the roles of free radicals in health and disease, the present paper overviews the current knowledge on the involvement of mitochondrial dysfunction in central nervous system diseases associated with neurodegeneration including Parkinson's and Huntington's disease as well as mitochondrial encephalopathies. The review puts special focus on the involvement and the potential therapeutic relevance of peroxisome proliferator-activated receptor-gamma coactivator 1-alpha (PGC-1α), a nuclear-encoded master regulator of mitochondrial biogenesis and antioxidant responses in these disorders, the transcriptional activation of which may hold novel therapeutic value as a more system-based approach aiming to restore mitochondrial functions in neurodegenerative processes.

摘要

某些线粒体呼吸复合体功能受损长期以来一直与帕金森病和亨廷顿舞蹈病等慢性神经退行性疾病的发病机制相关。此外,线粒体基因组或编码在维持线粒体正常功能中起关键作用的蛋白质的核基因发生遗传改变,可导致与神经退行性变和空泡性髓鞘病相关的严重全身性疾病的发生。目前,所有这些疾病都缺乏有效的疾病修饰疗法。在简要纪念阿尔伯特·圣捷尔吉教授之后,本文概述了目前关于线粒体功能障碍在与神经退行性变相关的中枢神经系统疾病(包括帕金森病、亨廷顿舞蹈病以及线粒体脑病)中的作用的知识。阿尔伯特·圣捷尔吉教授是细胞呼吸、抗氧化过程以及自由基在健康和疾病中的作用领域的先驱诺贝尔奖获得者。该综述特别关注过氧化物酶体增殖物激活受体γ共激活因子1α(PGC-1α)的参与情况及其潜在治疗相关性,PGC-1α是线粒体生物发生和抗氧化反应的核编码主要调节因子,在这些疾病中,其转录激活作为一种旨在恢复神经退行性过程中线粒体功能的更基于系统的方法可能具有新的治疗价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42c0/4537740/faf07b53460f/OMCL2015-498401.001.jpg

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