Iron: The redox-active center of oxidative stress in Alzheimer disease

被引:194
作者
Castellani, Rudy J.
Moreira, Paula I.
Liu, Gang
Dobson, Jon
Perry, George
Smith, Mark A.
Zhu, Xiongwei
机构
[1] Case Western Reserve Univ, Dept Pathol, Cleveland, OH 44106 USA
[2] Univ Texas, Coll Sci, San Antonio, TX 78285 USA
[3] Keele Univ, Inst Sci & Technol Med, Keele, Staffs, England
[4] Univ Utah, Dept Radiol, Salt Lake City, UT 84132 USA
[5] Univ Coimbra, Ctr Neurosci & Cell Biol Coimbra, Coimbra, Portugal
[6] Univ Maryland, Dept Pathol, Baltimore, MD 21201 USA
基金
美国国家卫生研究院;
关键词
Alzheimer disease; chelation; neurodegeneration; oxidative stress; redox active iron;
D O I
10.1007/s11064-007-9360-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Although iron is essential in maintaining the function of the central nervous system, it is a potent source of reactive oxygen species. Excessive iron accumulation occurs in many neurodegenerative diseases including Alzheimer disease (AD), Parkinson's disease, and Creutzfeldt-Jakob disease, raising the possibility that oxidative stress is intimately involved in the neurodegenerative process. AD in particular is associated with accumulation of numerous markers of oxidative stress; moreover, oxidative stress has been shown to precede hallmark neuropathological lesions early in the disease process, and such lesions, once present, further accumulate iron, among other markers of oxidative stress. In this review, we discuss the role of iron in the progression of AD.
引用
收藏
页码:1640 / 1645
页数:6
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