The role of iron as a mediator of oxidative stress in Alzheimer disease

被引:62
|
作者
Castellani, Rudy J. [1 ]
Moreira, Paula I. [2 ]
Perry, George [3 ,4 ]
Zhu, Xiongwei [4 ]
机构
[1] Univ Maryland, Dept Pathol, Baltimore, MD 21201 USA
[2] Univ Coimbra, Ctr Neurosci & Cell Biol Coimbra, Coimbra, Portugal
[3] Univ Texas San Antonio, Coll Sci, San Antonio, TX USA
[4] Case Western Reserve Univ, Dept Pathol, Cleveland, OH 44106 USA
关键词
Alzheimer disease; chelation; neurodegeneration; oxidative stress; redox active iron; AMYLOID PRECURSOR PROTEIN; REDOX-ACTIVE IRON; RAY-ABSORPTION SPECTROSCOPY; A-BETA; TRANSGENIC MICE; SENILE PLAQUES; MESSENGER-RNA; FREE-RADICALS; BRAIN-TISSUE; NEURODEGENERATIVE DISEASE;
D O I
10.1002/biof.1010
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
Iron is both essential for maintaining a spectrum of metabolic processes in the central nervous system and elsewhere, and potent source of reactive oxygen species. Redox balance with respect to iron, therefore, may be critical to human neurodegenerative disease but is also in need of better understanding. Alzheimer disease (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:133 / 138
页数:6
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