vo-ohpic and Alcoholism

Chronic alcohol consumption induces myocardial damage and a type of non-ischemic cardiomyopathy termed alcoholic cardiomyopathy, where mitochondrial ultrastructural damages and suppressed fusion activity promote cardiomyocyte apoptosis. The aim of the present study is to determine the role of mitochondrial fission proteins and/or other proteins that localise on cardiac mitochondria for apoptosis upon ethanol consumption. In vivo and in vitro chronic alcohol exposure increased mitochondrial Drp1 levels but knockdown of the same did not confer cardioprotection in H9c2 cells. These cells displayed downregulated expression of MFN2 and OPA1 for Bak-mediated cytochrome c release and apoptosis. Dysregulated PTEN/AKT cell survival signal in both ethanol treated and Drp1 knockdown cells augmented oxidative stress by promoting  mitochondrial PTEN-L and MFN1 interaction. Inhibiting this interaction with VO-OHpic, a reversible PTEN inhibitor, prevented Bak insertion into the mitochondria and release of cytochrome c to cytoplasm. Thus, our study provides evidence that Drp1-mediated mitochondrial fission is dispensable for ethanol-induced cardiotoxicity and that stress signals induce mitochondrial PTEN-L accumulation for structural and functional dyshomeostasis. Our in vivo results also demonstrates the therapeutic potential of VO-OHpic for habitual alcoholics developing myocardial dysfunction.

Topics: Alcoholism; Animals; Apoptosis; bcl-2 Homologous Antagonist-Killer Protein; Cardiomyopathy, Alcoholic; Cell Line; Cytochromes c; Disease Models, Animal; Dynamins; Ethanol; Female; Gene Expression Regulation; GTP Phosphohydrolases; Humans; Mitochondria, Heart; Mitochondrial Proteins; Myocardium; Myocytes, Cardiac; Organometallic Compounds; Proto-Oncogene Proteins c-akt; PTEN Phosphohydrolase; Rats; Rats, Wistar; RNA, Small Interfering; Signal Transduction