氧化应激
神经退行性变
活性氧
蛋白质聚集
化学
氧化磷酸化
过氧化氢
淀粉样蛋白(真菌学)
细胞生物学
生物化学
程序性细胞死亡
发病机制
生物
生物物理学
疾病
医学
免疫学
细胞凋亡
病理
无机化学
作者
Brian J. Tabner,Omar M. A. El-Agnaf,Matthew J. German,Nigel J. Fullwood,David Allsop
出处
期刊:Biochemical Society Transactions
[Portland Press]
日期:2005-10-01
卷期号:33 (5): 1082-1082
被引量:50
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.
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