Thiol-protease oxidation in age-related neuropathology

被引:4
作者
Guttmann, Rodney P. [1 ]
Ghoshal, Sarbani
机构
[1] Univ Kentucky, Dept Physiol, Dept Gerontol, Lexington, KY 40536 USA
关键词
Reactive oxygen species; Cell death; Redox regulation; Oxidative stress; Neurological disease; Free radicals; INSULIN-DEGRADING ENZYME; HYDROGEN-PEROXIDE; MATRIX METALLOPROTEINASES; ALZHEIMERS-DISEASE; SUMO MODIFICATION; REDOX REGULATION; CALPAIN ACTIVITY; MOLECULAR-BASIS; S-NITROSATION; STRESS;
D O I
10.1016/j.freeradbiomed.2011.04.017
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
Increased oxidative stress is a hallmark of every major neurodegenerative disease that has been studied. Numerous biomarkers of oxidative stress have been found, indicating that waves of oxidation had, at one time or another, overwhelmed antioxidant defenses, leaving behind a host of oxidized DNA, lipids, and proteins in their path. Although some level of oxidation may be beneficial, perhaps mediated by a hormetic response, the extent and types of oxidation detected in neuropathological states would suggest that oxidative stress contributes to a loss of homeostasis and cellular dysfunction. Although there are many targets of oxidants, this review emphasizes protein oxidation with a focus on an important group of redox-sensitive enzymes, the thiol-proteases. Both the direct and the indirect effects of oxidation and their potential importance in neurodegeneration are considered. Published by Elsevier Inc.
引用
收藏
页码:282 / 288
页数:7
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