Activation of mitochondrial ATP-dependent potassium channels by nitric oxide

Norihito Sasaki, Toshiaki Sato, Andreas Ohler, Brian O'Rourke, Eduardo Marbán

Research output: Contribution to journalArticle

Abstract

Background - Nitric oxide (NO) has been implicated as a mediator of 'second-window' ischemic preconditioning, and mitochondrial ATP-dependent K+ (mitoK(ATP)) channels are the likely effectors. The lines between NO and mitoK(ATP) channels are unknown. Methods and Results - We measured mitochondrial redox potential as an index of mitoK(ATP) channel opening in rabbit ventricular myocytes. The NO donor S-nitroso-N-acetyi-DL-penicillamine (SNAP, 0.1 to 1 mmol/L) oxidized the mitochondrial matrix dose-dependently without activating sarcolemmal K(ATP) channels. SNAP-induced oxidation was blocked by the selective mitoK(ATP) channel blocker 5-hydroxydecanoate and by the NO scavenger 2-(4-carboxyphenyl)-4,4',5,5'tetramethylimidazole-1-oxyl-3- oxide. SNAP-induced mitochondrial oxidation was detectable either by photomultiplier tube recordings of flavoprotein fluorescence or by confocal imaging. SNAP also enhanced the oxidative effects of diazoxide when both agents were applied together. Exposure to 1 mmol/L 8Br-cGMP failed to mimic the effects of SNAP. Conclusions - NO directly activates mitoK(ATP) channels and potentiates the ability of diazoxide to open these channels. These results provide novel mechanistic links between NO-induced cardioprotection and mitoK(ATP) channels.

Original languageEnglish (US)
Pages (from-to)439-445
Number of pages7
JournalCirculation
Volume101
Issue number4
DOIs
StatePublished - Feb 1 2000

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Keywords

  • Ischemic preconditioning
  • Mitochondria
  • Myocytes
  • Nitric oxide

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine
  • Physiology (medical)

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