Trends in Cardiovascular Medicine
Volume 19, Issue 5 , Pages 158-164, July 2009

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

  • Grant R. Budas
  • ,
  • Marie-Hélène Disatnik
  • ,
  • Daria Mochly-Rosen

      Affiliations

    • Corresponding Author InformationAddress correspondence to: Daria Mochly-Rosen, PhD, Department of Chemical and Systems Biology, Stanford University School of Medicine, CCSR, Rm 3145A, 269 Campus Drive, Stanford, CA 94305-5174, USA. Tel.: (+1) 650-725-7720

Department of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA 94305-5174, USA

Abstract 

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 ɛ 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.

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 This work was supported by NIAA11147 to DMR and in part, by an American Heart Association postdoctoral fellowship to GRB.

PII: S1050-1738(09)00145-5

doi:10.1016/j.tcm.2009.09.003

Trends in Cardiovascular Medicine
Volume 19, Issue 5 , Pages 158-164, July 2009