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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 EC₅₀ of 27 μmol/L but did not activate sarcolemmal K_ATP channels. The subcellular site of diazoxide …