In vivo studies on the toxic effects of microcystins on mitochondrial electron transport chain and ion regulation in liver and heart of rabbit

Comp Biochem Physiol C Toxicol Pharmacol. 2008 Sep;148(3):204-10. doi: 10.1016/j.cbpc.2008.05.008. Epub 2008 May 27.

Abstract

This study examined the toxic effects of microcystins on mitochondria of liver and heart of rabbit in vivo. Rabbits were injected i.p. with extracted microcystins (mainly MC-RR and -LR) at two doses, 12.5 and 50 MC-LReq. microg/kg bw, and the changes in mitochondria of liver and heart were studied at 1, 3, 12, 24 and 48 h after injection. MCs induced damage of mitochondrial morphology and lipid peroxidation in both liver and heart. MCs influenced respiratory activity through inhibiting NADH dehydrogenase and enhancing succinate dehydrogenase (SDH). MCs altered Na(+)-K(+)-ATPase and Ca(2+)-Mg(2+)-ATPase activities of mitochondria and consequently disrupted ionic homeostasis, which might be partly responsible for the loss of mitochondrial membrane potential (MMP). MCs were highly toxic to mitochondria with more serious damage in liver than in heart. Damage of mitochondria showed reduction at 48 h in the low dose group, suggesting that the low dose of MCs might have stimulated a compensatory response in the rabbits.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Electron Transport / drug effects*
  • Lipid Peroxidation / drug effects
  • Male
  • Malondialdehyde / metabolism
  • Microcystins / toxicity*
  • Mitochondria, Heart / drug effects*
  • Mitochondria, Heart / physiology
  • Mitochondria, Heart / ultrastructure
  • Mitochondria, Liver / drug effects*
  • Mitochondria, Liver / physiology
  • Mitochondria, Liver / ultrastructure
  • Rabbits
  • Sodium-Potassium-Exchanging ATPase / metabolism

Substances

  • Microcystins
  • Malondialdehyde
  • Sodium-Potassium-Exchanging ATPase