Mitochondrial Dysfunction And Myocardial Ischemia-Reperfusion: Implications For Novel Therapies

ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, VOL 57(2017)

引用 279|浏览11
暂无评分
摘要
Mitochondria have emerged as key participants in and regulators of myocardial injury during ischemia and reperfusion. This review examines the sites of damage to cardiac mitochondria during ischemia and focuses on the impact of these defects. The concept that mitochondrial damage during ischemia leads to cardiac injury during reperfusion is addressed. The mechanisms that translate ischemic mitochondrial injury into cellular damage, during both ischemia and early reperfusion, are examined. Next, we discuss strategies that modulate and counteract these mechanisms of mitochondrial-driven injury. The new concept that mitochondria are not merely stochastic sites of oxidative and calcium-mediated injury but that they activate cellular responses of mitochondrial remodeling and cellular reactions that modulate the balance between cell death and recovery is reviewed, and the therapeutic implications of this concept are discussed.
更多
查看译文
关键词
oxidative phosphorylation,electron transport chain,reactive oxygen species,cardiolipin,fatty acid oxidation,ubiquinol: cytochrome c oxidoreductase
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要