Restoration of Ca2+-inhibited oxidative phosphorylation in cardiac mitochondria by mitochondrial Ca2+ unloading

Mol Cell Biochem. 2001 Apr;220(1-2):135-40. doi: 10.1023/a:1010894427373.

Abstract

Mitochondria, the major source of cellular ATP, display high vulnerability to metabolic stress, in particular to excessive Ca2+ loading. Here, we show that Ca2+-inhibited mitochondrial ATP generation could be restored through stimulated Ca2+ discharge from mitochondrial matrix. This was demonstrated using a Ca2+ ionophore or through Na+/Ca2+ exchange-mediated decrease of mitochondrial Ca2+ load. Furthermore, diazoxide, a mitochondrial potassium channel opener, which maintained mitochondrial Ca2+ homeostasis, also restored Ca2+-inhibited ATP synthesis and preserved the structural integrity of Ca2+-challenged mitochondria. Thus, under conditions of excessive mitochondrial Ca2+ overload targeting mitochondrial Ca2+ transport pathways restores oxidative phosphorylation required for vital cellular processes. This study, therefore, identifies an effective strategy capable to rescue Ca2+-disrupted mitochondrial energetics.

Publication types

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

MeSH terms

  • Adenosine Triphosphate / biosynthesis
  • Adenosine Triphosphate / metabolism
  • Animals
  • Calcium / metabolism*
  • Diazoxide / pharmacology
  • Dose-Response Relationship, Drug
  • Inhibitory Concentration 50
  • Microscopy, Electron
  • Mitochondria / metabolism*
  • Myocardium / metabolism
  • Oxygen / metabolism*
  • Phosphorylation
  • Potassium Channels / metabolism
  • Rats
  • Time Factors
  • Vasodilator Agents / pharmacology

Substances

  • Potassium Channels
  • Vasodilator Agents
  • Adenosine Triphosphate
  • Diazoxide
  • Oxygen
  • Calcium