Oxidative stress and Parkinson's disease

被引:643
作者
Blesa, Javier [1 ]
Trigo-Damas, Ines [1 ]
Quiroga-Varela, Anna [2 ]
Jackson-Lewis, Vernice R. [3 ]
机构
[1] CEU San Pablo Univ, Hosp Madrid, Ctr Integralde Neurociencias AC, Mostoles & Med Sch,HM Puerta Sur, Madrid 28938, Spain
[2] Univ Perugia, Osped Santa Maria Misericordia, Dept Med, Neurol Clin, I-06100 Perugia, Italy
[3] Columbia Univ, Dept Pathol & Cell Biol, New York, NY USA
来源
FRONTIERS IN NEUROANATOMY | 2015年 / 9卷
关键词
mitochondrial dysfunction; dopamine; neuroinflammation; Parkinson disease; oxidative stress; MITOCHONDRIAL COMPLEX-I; HUMAN SUBSTANTIA-NIGRA; MICROGLIA-MEDIATED NEUROTOXICITY; ALPHA-SYNUCLEIN; RESPIRATORY-CHAIN; NADPH OXIDASE; PARS-COMPACTA; PROTEIN DJ-1; TYROSINE-HYDROXYLASE; INDUCED DEGENERATION;
D O I
10.3389/fnana.2015.00091
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Parkinson disease (PD) is a chronic, progressive neurological disease that is associated with a loss of dopaminergic neurons in the substantia nigra pars compacta of the brain. The molecular mechanisms underlying the loss of these neurons still remain elusive. Oxidative stress is thought to play an important role in dopaminergic neurotoxicity. Complex I deficiencies of the respiratory chain account for the majority of unfavorable neuronal degeneration in PD. Environmental factors, such as neurotoxins, pesticides, insecticides, dopamine (DA) itself, and genetic mutations in PD-associated proteins contribute to mitochondrial dysfunction which precedes reactive oxygen species formation. In this mini review, we give an update of the classical pathways involving these mechanisms of neurodegeneration, the biochemical and molecular events that mediate or regulate DA neuronal vulnerability, and the role of PD-related gene products in modulating cellular responses to oxidative stress in the course of the neurodegenerative process.
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页数:9
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