Oxidatively modified proteins in aging and disease

被引:646
|
作者
Beal, MF [1 ]
机构
[1] Cornell Univ, Weill Med Col, Dept Neurol & Neurosci, New York Presbyterian Hosp, New York, NY USA
基金
美国国家卫生研究院;
关键词
3-nitrotyrosine; carbonyls; dityrosine; Alzheimer's; Parkinson's; Huntington's; amyotrophic lateral sclerosis; free radical;
D O I
10.1016/S0891-5849(02)00780-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
There is a large body of evidence implicating oxidative damage in the pathogenesis of both normal aging and neurodegenerative diseases. Oxidative damage to proteins has been well established. Although there are a large number of potential oxidative modifications only a few have been systematically studied. The most frequently studied marker of oxidative damage to proteins is protein carbonyl groups. 3-Nitrotyrosine is thought to be a relatively specific marker of oxidative damage mediated by peroxyrritrite. Increased concentrations of both protein carbonyls and 3-nitrotyrosine have been documented in both normal aging as well as in Alzheimer's disease (AD), Parkinson's disease (PD), and amyotrophic lateral sclerosis (ALS). These findings help to provide a rationale for trials of antioxidants in neurodegenerative diseases. (C) 2002 Elsevier Science Inc.
引用
收藏
页码:797 / 803
页数:7
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