Mitochondrial dysfunction in human pathologies

被引:51
作者
Monsalve, Maria
Borniquel, Sara
Valle, Inmaculada
Lamas, Santiago
机构
[1] Inst Salud Carlos III, Ctr Nacl Invest Cardiovasc, Madrid 28029, Spain
[2] CSIC, Ctr Invest Biol, Madrid 28040, Spain
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2007年 / 12卷
关键词
neurological diseases; Parkinson disease; Alzhemer disease; Huntington disease; epilepsy; atheroesclerosis; diabetes; cancer; aging; review; NF-KAPPA-B; HYDROPEROXIDE GLUTATHIONE-PEROXIDASE; CYTOCHROME-C-OXIDASE; ANTIOXIDANT RESPONSE ELEMENT; EARLY EMBRYONIC LETHALITY; UNCOUPLING PROTEIN-2 PROTECTS; CU/ZN-SUPEROXIDE DISMUTASE; ALZHEIMERS-DISEASE BRAIN; INDUCED UP-REGULATION; HEAT-SHOCK PROTEINS;
D O I
10.2741/2132
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
The integrity of mitochondrial function is fundamental to cell life. The cell demands for mitochondria and their complex integration into cell biology, extends far beyond the provision of ATP. It follows that disturbances of mitochondrial function lead to disruption of cell function, expressed as disease or even death. Mitochondria are major producers of free radical species and also possibly of nitric oxide, and are, at the same time, major targets for oxidative damage. In this review we consider recent developments in our knowledge of how the mitochondrial production of reactive oxygen species ( ROS) plays a critical role in several major human pathologies. We will also consider recent advances in our understanding of the molecular mechanisms involved in mitochondrial ROS detoxification.
引用
收藏
页码:1131 / 1153
页数:23
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