Defining mitochondrial targets to combat the pleiotropic effects of toxic oxidative stress

被引:214
作者
Fariss, MW [1 ]
Chan, CB
Patel, M
Van Houten, B
Orrenius, S
机构
[1] Univ Colorado, Hlth Sci Ctr, Dept Pharmaceut Sci, Denver, CO 80262 USA
[2] Univ Colorado, Hlth Sci Ctr, Ctr Canc, Denver, CO 80262 USA
[3] Univ Prince Edward Isl, Dept Biomed Sci, Charlottetown, PE C1A 4P3, Canada
[4] Univ Colorado, Hlth Sci Ctr, Program Neurosci, Denver, CO 80262 USA
[5] NIEHS, Genet Mol Lab, NIH, Res Triangle Pk, NC 27709 USA
[6] Karolinska Inst, Inst Environm Med, Div Toxicol, SE-17177 Stockholm, Sweden
关键词
D O I
10.1124/mi.5.2.7
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
Oxidative stress and mitochondrial oxidative damage have been implicated in the etiology of numerous common diseases. The critical mitochondrial events responsible for oxidative stress-mediated cell death (toxic oxidative stress), however, have yet to be defined. Several oxidative events implicated in toxic oxidative stress include alterations in mitochondrial lipids (e.g. cardiolipin), mitochondrial DNA, and mitochondrial proteins (eg. aconitase and uncoupling protein 2). Furthermore, recent findings indicate the enrichment of mitochondrial membranes with vitamin E protects cells against the toxic effects of oxidative stress. This review briefly summarizes the role of these mitochondrial events in toxic oxidative stress, including: 1) the protective role of mitochondrial vitamin E in toxic oxidative stress, 2) the role of mitochondrial DNA in toxic oxidative stress, 3) the interaction between cardiolipin and cytochrome c in mitochondrial regulation of apoptosis, 4) the role of mitochondrial aconitase in oxidative neurodegeneration, and 5) the role of mitochondrial uncoupling protein 2 in the pathogenesis of type 2 diabetes.
引用
收藏
页码:94 / 111
页数:18
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