Mechanism of Oxidative Stress in Neurodegeneration

被引:723
作者
Gandhi, Sonia [1 ]
Abramov, Andrey Y. [1 ]
机构
[1] UCL Inst Neurol, Dept Mol Neurosci, London WC1N 3BG, England
关键词
AMYLOID-BETA PEPTIDE; NADPH OXIDASE; MITOCHONDRIAL DYSFUNCTION; PARKINSONS-DISEASE; ALPHA-SYNUCLEIN; CELL-DEATH; COMPLEX-I; A-BETA; UNCOUPLING PROTEIN-2; RESPIRATORY-CHAIN;
D O I
10.1155/2012/428010
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Biological tissues require oxygen to meet their energetic demands. However, the consumption of oxygen also results in the generation of free radicals that may have damaging effects on cells. The brain is particularly vulnerable to the effects of reactive oxygen species due to its high demand for oxygen, and its abundance of highly peroxidisable substrates. Oxidative stress is caused by an imbalance in the redox state of the cell, either by overproduction of reactive oxygen species, or by dysfunction of the antioxidant systems. Oxidative stress has been detected in a range of neurodegenerative disease, and emerging evidence from in vitro and in vivo disease models suggests that oxidative stress may play a role in disease pathogenesis. However, the promise of antioxidants as novel therapies for neurodegenerative diseases has not been borne out in clinical studies. In this review, we critically assess the hypothesis that oxidative stress is a crucial player in common neurodegenerative disease and discuss the source of free radicals in such diseases. Furthermore, we examine the issues surrounding the failure to translate this hypothesis into an effective clinical treatment.
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页数:11
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