Possible mechanism for formation and regulation of the palmitate-induced cyclosporin A-insensitive mitochondrial pore

Biochemistry (Mosc). 2005 Jul;70(7):815-21. doi: 10.1007/s10541-005-0189-x.

Abstract

The mechanism of the palmitate-induced opening of the mitochondrial Ca2+-dependent cyclosporin A (CsA)-insensitive pore was studied, as well as the influence on this process of well-known modulators of the CsA-sensitive Ca2+-dependent pore. Palmitic acid, which can bind Ca2+ with high affinity, induced the cyclosporin A-insensitive swelling of mitochondria, whereas palmitoleic and 2-bromopalmitic acids, which have no such affinity for Ca2+, failed to induce the pore opening. The palmitate-induced Ca2+-dependent swelling of mitochondria was not affected by a well-known inhibitor of the CsA-sensitive pore (ADP) and an activator of this pore (inorganic phosphate, P(i)). However, this swelling was inhibited by physiological concentrations of ATP ([I]50 = 1.3 mM), but 100 microM ATP increased by 30% the rate of mitochondria swelling if Ca2+ had been added earlier. The effects of ATP (inhibition and activation) manifested themselves from different sides of the inner mitochondrial membrane. Mg2+ inhibited the palmitate-induced Ca2+-dependent swelling of mitochondria with [I]50 = 0.8 mM. It is concluded that palmitic acid induces the opening of the CsA-insensitive pore due to its ability for complexing with Ca2+. A possible mechanism of the pore formation and the influence of some modulators on this process are discussed.

Publication types

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

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Adenosine Triphosphate / pharmacology
  • Animals
  • Calcium / metabolism
  • Calcium / pharmacology
  • Cyclosporine / pharmacology
  • Dose-Response Relationship, Drug
  • Fatty Acids, Nonesterified / metabolism
  • Fatty Acids, Nonesterified / pharmacology
  • Intracellular Membranes / drug effects
  • Intracellular Membranes / physiology
  • Ion Channel Gating / drug effects*
  • Ion Channel Gating / physiology
  • Ion Channels / drug effects*
  • Ion Channels / metabolism
  • Liposomes / metabolism
  • Magnesium / pharmacology
  • Mitochondria, Liver / drug effects
  • Mitochondria, Liver / metabolism*
  • Mitochondrial Membrane Transport Proteins
  • Mitochondrial Permeability Transition Pore
  • Mitochondrial Swelling / drug effects
  • Mitochondrial Swelling / physiology
  • Palmitic Acid / antagonists & inhibitors
  • Palmitic Acid / metabolism
  • Palmitic Acid / pharmacology*
  • Rats

Substances

  • Fatty Acids, Nonesterified
  • Ion Channels
  • Liposomes
  • Mitochondrial Membrane Transport Proteins
  • Mitochondrial Permeability Transition Pore
  • Palmitic Acid
  • Cyclosporine
  • Adenosine Triphosphate
  • Magnesium
  • Calcium