Mitochondrial K(ATP) channel activation reduces anoxic injury by restoring mitochondrial membrane potential

Am J Physiol Heart Circ Physiol. 2001 Sep;281(3):H1295-303. doi: 10.1152/ajpheart.2001.281.3.H1295.

Abstract

Mitochondrial membrane potential (DeltaPsi(m)) is severely compromised in the myocardium after ischemia-reperfusion and triggers apoptotic events leading to cell demise. This study tests the hypothesis that mitochondrial ATP-sensitive K(+) (mitoK(ATP)) channel activation prevents the collapse of DeltaPsi(m) in myocytes during anoxia-reoxygenation (A-R) and is responsible for cell protection via inhibition of apoptosis. After 3-h anoxia and 2-h reoxygenation, the cultured myocytes underwent extensive damage, as evidenced by decreased cell viability, compromised membrane permeability, increased apoptosis, and decreased ATP concentration. Mitochondria in A-R myocytes were swollen and fuzzy as shown after staining with Mito Tracker Orange CMTMRos and in an electron microscope and exhibited a collapsed DeltaPsi(m), as monitored by 5,5',6,6'-tetrachloro-1,1',3,3'-tetraethylbenzimidazolcarbocyanine iodide (JC-1). Cytochrome c was released from mitochondria into the cytosol as demonstrated by cytochrome c immunostaining. Activation of mitoK(ATP) channel with diazoxide (100 micromol/l) resulted in a significant protection against mitochondrial damage, ATP depletion, cytochrome c loss, and stabilized DeltaPsi(m). This protection was blocked by 5-hydroxydecanoate (500 micromol/l), a mitoK(ATP) channel-selective inhibitor, but not by HMR-1098 (30 micromol/l), a putative sarcolemmal K(ATP) channel-selective inhibitor. Dissipation of DeltaPsi(m) also leads to opening of mitochondrial permeability transition pore, which was prevented by cyclosporin A. The data support the hypothesis that A-R disrupts DeltaPsi(m) and induces apoptosis, which are prevented by the activation of the mitoK(ATP) channel. This further emphasizes the therapeutic significance of mitoK(ATP) channel agonists in the prevention of ischemia-reperfusion cell injury.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Animals, Newborn
  • Apoptosis* / drug effects
  • Benzamides / pharmacology
  • Cell Hypoxia / drug effects
  • Cell Survival / drug effects
  • Cells, Cultured
  • Cytochrome c Group / metabolism
  • Cytoprotection / drug effects
  • Decanoic Acids / pharmacology
  • Diazoxide / pharmacology
  • Hydroxy Acids / pharmacology
  • In Situ Nick-End Labeling
  • Membrane Potentials / drug effects
  • Membrane Potentials / physiology
  • Mitochondria, Heart / drug effects
  • Mitochondria, Heart / metabolism*
  • Myocardium / cytology
  • Myocardium / metabolism
  • Potassium Channel Blockers
  • Potassium Channels / metabolism*
  • Rats
  • Vasodilator Agents / pharmacology

Substances

  • Benzamides
  • Cytochrome c Group
  • Decanoic Acids
  • Hydroxy Acids
  • Potassium Channel Blockers
  • Potassium Channels
  • Vasodilator Agents
  • 5-hydroxydecanoic acid
  • HMR 1098
  • Diazoxide