The role of mitochondrial membrane potential in ischemic heart failure

Mitochondrion. 2011 Sep;11(5):700-6. doi: 10.1016/j.mito.2011.06.001. Epub 2011 Jun 16.

Abstract

The molecular events occurring during myocardial infarction and cardioprotection are described with an emphasis on the changes of the mitochondrial membrane potential (ΔΨ(m)). The low ΔΨ(m) values of the normal beating heart (100-140 mV) are explained by the allosteric ATP-inhibition of cytochrome c oxidase (CcO) through feedback inhibition by ATP at high [ATP]/[ADP] ratios. During ischemia the mechanism is reversibly switched off by signaling through reactive oxygen species (ROS). At reperfusion high ΔΨ(m) values cause a burst of ROS production leading to apoptosis and/or necrosis. Ischemic preconditioning is suggested to cause additional phosphorylation of CcO, protecting the enzyme from immediate dephosphorylation via ROS signaling.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Allosteric Regulation
  • Animals
  • Cytoprotection
  • Electron Transport Complex IV / antagonists & inhibitors
  • Electron Transport Complex IV / metabolism
  • Heart Failure / metabolism*
  • Heart Failure / physiopathology
  • Humans
  • Membrane Potential, Mitochondrial*
  • Mitochondria, Heart / metabolism
  • Mitochondria, Heart / pathology
  • Myocardial Ischemia / metabolism*
  • Myocardial Ischemia / physiopathology
  • Myocardial Reperfusion Injury / metabolism
  • Myocardial Reperfusion Injury / physiopathology
  • Oxygen Consumption
  • Permeability
  • Reactive Oxygen Species / metabolism
  • Signal Transduction

Substances

  • Reactive Oxygen Species
  • Adenosine Triphosphate
  • Electron Transport Complex IV