Protein aggregation, metals and oxidative stress in neurodegenerative diseases

被引:85
|
作者
Tabner, BJ [1 ]
El-Agnaf, OMA
German, MJ
Fullwood, NJ
Allsop, D
机构
[1] Univ Lancaster, Dept Biol Sci, Lancaster LA1 4YQ, England
[2] Univ Lancaster, Magnet Resonance Lab, Lancaster LA1 4YQ, England
[3] United Arab Emirates Univ, Fac Med & Hlth Sci, Dept Biochem, Al Ain, U Arab Emirates
[4] Univ Lancaster, Dept Phys, Lancaster LA1 4YQ, England
基金
英国惠康基金;
关键词
amyloid; hydrogen peroxide; metal; neurodegeneration; oligomer; oxidative stress;
D O I
10.1042/BST0331082
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 clear evidence implicating oxidative stress in the pathology of many different neurodegenerative diseases. ROS (reactive oxygen species) are the primary mediators of oxidative stress and many of the aggregating proteins and peptides associated with neurodegenerative disease can generate hydrogen peroxide, a key ROS, apparently through interactions with redox-active metal ions. our recent results suggest that ROS are generated during the very early stages of protein aggregation, when protofibrils or soluble oligomers are present, but in the absence of mature amyloid fibrils. The generation of ROS during early-stage protein aggregation may be a common, fundamental molecular mechanism underlying the pathogenesis of oxidative damage, neurodegeneration and cell death in several different neurodegenerative diseases. Drugs that specifically target this process could be useful in the future therapy of these diseases.
引用
收藏
页码:1082 / 1086
页数:5
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