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帕金森病、胰岛素抵抗与神经保护新制剂。

Parkinson's disease, insulin resistance and novel agents of neuroprotection.

机构信息

Sobell Department of Motor Neuroscience, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK.

出版信息

Brain. 2013 Feb;136(Pt 2):374-84. doi: 10.1093/brain/aws009. Epub 2012 Feb 17.

DOI:10.1093/brain/aws009
PMID:22344583
Abstract

Multiple avenues of research including epidemiology, molecular genetics and cell biology have identified links between Parkinson's disease and type 2 diabetes mellitus. Several recent discoveries have highlighted common cellular pathways that potentially relate neurodegenerative processes with abnormal mitochondrial function and abnormal glucose metabolism. This includes converging evidence identifying that peroxisome proliferator activated receptor gamma coactivator 1-α, a key regulator of enzymes involved in mitochondrial respiration and insulin resistance, is potentially pivotal in the pathogenesis of neurodegeneration in Parkinson's disease. This evidence supports further study of these pathways, most importantly to identify neuroprotective agents for Parkinson's disease, and/or establish more effective prevention or treatment for type 2 diabetes mellitus. In parallel with these advances, there are already randomized trials evaluating several established treatments for insulin resistance (pioglitazone and exenatide) as possible disease modifying drugs in Parkinson's disease, with only preliminary insights regarding their mechanisms of action in neurodegeneration, which may be effective in both disease processes through an action on mitochondrial function. Furthermore, parallels are also emerging between these same pathways and neurodegeneration associated with Alzheimer's disease and Huntington's disease. Our aim is to highlight this converging evidence and stimulate further hypothesis-testing studies specifically with reference to the potential development of novel neuroprotective agents in Parkinson's disease.

摘要

包括流行病学、分子遗传学和细胞生物学在内的多种研究途径已经确定了帕金森病与 2 型糖尿病之间的联系。最近的一些发现强调了潜在的共同细胞途径,这些途径可能与神经退行性过程、异常线粒体功能和异常葡萄糖代谢有关。这包括越来越多的证据表明,过氧化物酶体增殖物激活受体γ共激活因子 1-α(一种参与线粒体呼吸和胰岛素抵抗的酶的关键调节因子)在帕金森病的神经退行性发病机制中可能具有关键作用。这一证据支持进一步研究这些途径,最重要的是确定帕金森病的神经保护剂,或建立更有效的 2 型糖尿病预防或治疗方法。随着这些进展,已经有几项针对胰岛素抵抗的既定治疗方法(吡格列酮和 exenatide)的随机试验正在评估其作为帕金森病可能的疾病修饰药物的作用,这些药物在神经退行性变中的作用机制仅初步了解,可能通过对线粒体功能的作用在两种疾病过程中都有效。此外,这些相同途径与阿尔茨海默病和亨廷顿病相关的神经退行性变之间也出现了相似之处。我们的目的是强调这一趋同证据,并激发进一步的假设检验研究,特别是针对帕金森病中新型神经保护剂的潜在开发。

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