Ibuprofen-induced liver mitochondrial permeability transition

Toxicol Lett. 2000 Jan 5;111(3):213-8. doi: 10.1016/s0378-4274(99)00180-0.

Abstract

This study examined the effect of the nonsteroidal anti-inflammatory drug ibuprofen on liver inner mitochondrial membrane permeability transition in the presence of Ca2+ and phosphate. Incubation of isolated liver mitochondria with ibuprofen (0.1-0.4 mM) induced inner mitochondrial membrane permeability as indicated by loss of inner mitochondrial membrane potential, swelling of matrix and loss of pre-accumulated Ca2+. The presence of cyclosporin A (1 microM) in the incubation medium preventing ibuprofen from causing loss of inner mitochondrial membrane potential, swelling and loss of pre-accumulated Ca2+. It is concluded that ibuprofen acted as an activator of Ca2+ and phosphate in promoting the opening of inner mitochondrial membrane pore.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / toxicity*
  • Calcium / metabolism
  • Cyclosporine / toxicity
  • Ibuprofen / toxicity*
  • Immunosuppressive Agents / toxicity
  • In Vitro Techniques
  • Indicators and Reagents
  • Male
  • Membrane Potentials / drug effects
  • Mitochondria, Liver / drug effects*
  • Mitochondria, Liver / metabolism
  • Mitochondrial Swelling / drug effects
  • Onium Compounds
  • Organophosphorus Compounds
  • Permeability / drug effects
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Immunosuppressive Agents
  • Indicators and Reagents
  • Onium Compounds
  • Organophosphorus Compounds
  • Cyclosporine
  • Calcium
  • tetraphenylphosphonium
  • Ibuprofen