Mitochondrial targets of drug toxicity

被引:327
作者
Wallace, KB [1 ]
Starkov, AA [1 ]
机构
[1] Univ Minnesota, Sch Med, Dept Biochem & Mol Biol, Duluth, MN 55812 USA
关键词
oxidative phosphorylation; uncouplers; bioenergetics; permeability transition; redox cycling;
D O I
10.1146/annurev.pharmtox.40.1.353
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Mitochondria have long been recognized as the generators of energy for the cell. Like any other power source, however, mitochondria are highly vulnerable to inhibition or uncoupling of the energy harnessing process and run a high risk for catastrophic damage to the cell. The exquisite structural and functional characteristics of mitochondria provide a number of primary targets for xenobiotic-induced bioenergetic failure. They also provide opportunities for selective delivery of drugs to the mitochondrion. In light of the large number of natural, commercial, pharmaceutical, and environmental chemicals that manifest their toxicity by interfering with mitochondrial bioenergetics, it is important to understand the underlying mechanisms. The significance is further underscored by the recent identification of bioenergetic control points for cell replication and differentiation and the realization that mitochondria play a determinant role in cell signaling and apoptotic modes of cell death.
引用
收藏
页码:353 / 388
页数:36
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