Contribution of apoptosis in myocardial reperfusion injury and loss of cardioprotection in diabetes mellitus

被引:74
作者
Badalzadeh, Reza [1 ,2 ,3 ]
Mokhtari, Behnaz [3 ]
Yavari, Raana [3 ]
机构
[1] Tabriz Univ Med Sci, Cardiovasc Res Ctr, Tabriz, Iran
[2] Tabriz Univ Med Sci, Drug Appl Res Ctr, Tabriz, Iran
[3] Tabriz Univ Med Sci, Dept Physiol, Fac Med, Tabriz, Iran
关键词
Myocardial reperfusion injury; Apoptosis; Diabetes; Preconditioning; Postconditioning; PERMEABILITY TRANSITION PORE; ACTIVATED PROTEIN-KINASE; ISCHEMIA/REPERFUSION-INJURY; INFARCT SIZE; NITRIC-OXIDE; MITOCHONDRIAL DYSFUNCTION; CARDIOMYOCYTE APOPTOSIS; CARDIAC FIBROBLASTS; CARDIOVASCULAR RISK; THERAPEUTIC TARGET;
D O I
10.1007/s12576-015-0365-8
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Ischemic heart disease is one of the major causes of death worldwide. Ischemia is a condition in which blood flow of the myocardium declines, leading to cardiomyocyte death. However, reperfusion of ischemic regions decreases the rate of mortality, but it can also cause later complications. In a clinical setting, ischemic heart disease is always coincident with other co-morbidities such as diabetes. The risk of heart disease increases 2-3 times in diabetic patients. Apoptosis is considered to be one of the main pathophysiological mechanisms of myocardial ischemia-reperfusion injury. Diabetes can disrupt the anti-apoptotic intracellular signaling cascades involved in myocardial protection. Therefore, targeting these changes may be an effective cardioprotective approach in the diabetic myocardium against ischemia-reperfusion injury. In this article, we review the interaction of diabetes with the pathophysiology of myocardial ischemia-reperfusion injury, focusing on the contribution of apoptosis in this context, and then discuss the alterations of pro-apoptotic or anti-apoptotic pathways probably responsible for the loss of cardioprotection in diabetes.
引用
收藏
页码:201 / 215
页数:15
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