Mitochondrial ATP-dependent potassium channels - Novel effectors of cardioprotection?

Article

关键词: ISOLATED RABBIT CARDIOMYOCYTES;    ACTION-POTENTIAL DURATION;    SENSITIVE K+ CHANNEL;    VENTRICULAR MYOCYTES;    RUTHENIUM RED;    RAT-LIVER;    HEART;    MEMBRANE;    INJURY;    OPENER;   

DOI  :  10.1161/01.CIR.97.24.2463

来源: SCIE

【 摘 要 】

Background-Brief interruptions of coronary blood flow paradoxically protect the heart from subsequent prolonged ischemia. The basis of such endogenous cardioprotection, known as ischemic preconditioning, remains uncertain. Pharmacological evidence has implicated ATP-dependent potassium (K-ATP) channels in the mechanism of preconditioning; however, the effects of sarcolemmal K-ATP channels on excitability cannot account for the protection. Methods and Results-We simultaneously measured flavoprotein fluorescence, an index of mitochondrial redox state, and sarcolemmal K-ATP currents in intact rabbit ventricular myocytes, Our results show that diazoxide, a K-ATP channel opener, selectively activates mitochondrial K-ATP channels. Diazoxide induced reversible oxidation of flavoproteins with an EC,, of 27 mu mol/L but did not activate sarcolemmal K-ATP channels. The subcellular site of diazoxide action is further localized to mitochondria by confocal imaging of fluorescence arising from flavoproteins and tetramethylrhodamine ethyl eater, In a cellular model of simulated ischemia, inclusion of diazoxide decreased the rate of cell death to about half of that in controls. Both the redox changes and protection are inhibited by the K-ATP channel blocker 5-hydroxydecanoic acid. Conclusions-Our results demonstrate that diazoxide targets mitochondrial but not sarcolemmal K-ATP channels and imply that mitochondrial K-ATP channels may mediate the protection from K-ATP channel openers.

【 授权许可】

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