Mitochondrial dysfunction and oxidative stress in Parkinson's disease and monogenic parkinsonism

被引:359
作者
Hauser, David N. [1 ,2 ]
Hastings, Teresa G. [3 ,4 ,5 ]
机构
[1] NIA, Cell Biol & Gene Express Unit, Neurogenet Lab, NIH, Bethesda, MD 20892 USA
[2] Brown Univ, NIH, Grad Partnership Program, Dept Neurosci, Providence, RI 02912 USA
[3] Univ Pittsburgh, Pittsburgh Inst Neurodegenerat Dis, Pittsburgh, PA 15260 USA
[4] Univ Pittsburgh, Dept Neurol, Pittsburgh, PA 15260 USA
[5] Univ Pittsburgh, Dept Neurosci, Pittsburgh, PA USA
关键词
Parkinson's disease; Mitochondria; Oxidative stress; Dopamine oxidation; RAT-BRAIN MITOCHONDRIA; COMPLEX-I DEFICIENCY; RESOLUTION CRYSTAL-STRUCTURE; CYSTEINE-SULFINIC ACID; SUBSTANTIA-NIGRA; ALPHA-SYNUCLEIN; DOPAMINERGIC-NEURONS; DJ-1-DEFICIENT MICE; DNA DELETIONS; FAMILIAL PARKINSONISM;
D O I
10.1016/j.nbd.2012.10.011
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The pathogenic mechanisms that underlie Parkinson's disease remain unknown. Here, we review evidence from both sporadic and genetic forms of Parkinson's disease that implicate both mitochondria and oxidative stress as central players in disease pathogenesis. A systemic deficiency in complex I of the mitochondrial electron transport chain is evident in many patients with the disease. Oxidative stress caused by reactive metabolites of dopamine and alterations in the levels of iron and glutathione in the substantia nigra accompany this mitochondrial dysfunction. Recent evidence from studies on the genetic forms of parkinsonism with particular stress on DJ-1, parkin, and PINK-1 also suggest the involvement of mitochondria and oxidative stress. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:35 / 42
页数:8
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