Calcium and Mitochondrial Reactive Oxygen Species Generation: How to Read the Facts

被引:189
作者
Adam-Vizi, Vera [1 ]
Starkov, Anatoly A. [2 ]
机构
[1] Semmelweis Univ, Dept Med Biochem, Neurobiochem Grp, Hungarian Acad Sci, H-1094 Budapest, Hungary
[2] Cornell Univ, Weill Med Coll, New York, NY 10021 USA
关键词
Calcium; mitochondria; permeability transition; reactive oxygen species; ALPHA-KETOGLUTARATE DEHYDROGENASE; PERMEABILITY TRANSITION PORE; AMYLOID-BETA-PEPTIDE; HYDROGEN-PEROXIDE PRODUCTION; ASCITES TUMOR MITOCHONDRIA; OXIDOREDUCTASE COMPLEX-I; TRANSGENIC MOUSE MODEL; RAT-BRAIN MITOCHONDRIA; OXIDATIVE STRESS; ALZHEIMERS-DISEASE;
D O I
10.3233/JAD-2010-100465
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A number of recent discoveries indicate that abnormal Ca2+ signaling, oxidative stress, and mitochondrial dysfunction are involved in the neuronal damage in Alzheimer's disease. However, the literature on the interactions between these factors is controversial especially in the interpretation of the cause-effect relationship between mitochondrial damage induced by Ca2+ overload and the production of reactive oxygen species (ROS). In this review, we survey the experimental observations on the Ca2+-induced mitochondrial ROS production, explain the sources of controversy in interpreting these results, and discuss the different molecular mechanisms underlying the effect of Ca2+ on the ROS emission by brain mitochondria.
引用
收藏
页码:S413 / S426
页数:14
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