Aldehyde Dehydrogenase 2 in Cardiac Protection: A New Therapeutic Target?

被引:98
作者
Budas, Grant R. [1 ]
Disatnik, Marie-Helene [1 ]
Mochly-Rosen, Dana [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Chem & Syst Biol, CCSR, Stanford, CA 94305 USA
关键词
MITOCHONDRIAL PERMEABILITY TRANSITION; NITRIC-OXIDE; LIPID-PEROXIDATION; INDUCED CARDIOPROTECTION; GLYCERYL TRINITRATE; REPERFUSION INJURY; EPSILON-PKC; HEART; NITROGLYCERIN; ACTIVATION;
D O I
10.1016/j.tcm.2009.09.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Mitochondrial aldehyde dehydrogenase 2 (ALDH2) is emerging as a key enzyme involved in cytoprotection in the heart. ALDH2 mediates both the detoxification of reactive aldehydes such as acetaldehyde and 4-hydroxy-2-nonenal and the bioactivation of nitroglycerin to nitric oxide. In addition, chronic nitrate treatment results in ALDH2 inhibition and contributes to nitrate tolerance. Our laboratory recently identified ALDH2 to be a key mediator of endogenous cytoprotection. We reported that ALDH2 is phosphorylated and activated by the survival kinase protein kinase C epsilon and found a strong inverse correlation between ALDH2 activity and infarct size. We also identified a small molecule ALDH2 activator which reduces myocardial infarct size induced by ischemia/reperfusion in vivo. In this review, we discuss evidence that ALDH2 is a key mediator of endogenous survival signaling in the heart, suggest possible cardioprotective mechanisms mediated by ALDH2 and discuss potential clinical implications of these findings. (Trends Cardiovasc Med 2009;19:158-164) (C) 2009, Elsevier Inc.
引用
收藏
页码:158 / 164
页数:7
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