The crucial role of hypoxia in halothane-induced lipid peroxidation

Biochem Biophys Res Commun. 1984 Feb 29;119(1):139-43. doi: 10.1016/0006-291x(84)91629-2.

Abstract

Halothane-induced lipid peroxidation in NADPH-reduced liver microsomes from phenobarbital-pretreated male rats was studied under defined steady state oxygen partial pressures (Po2). Under anaerobic conditions, as well as at a Po2 above 10 mm Hg no halothane-induced formation of malondialdehyde was detected. At a Po2 below 10 mm Hg, however, with a maximum near 1 mm Hg oxygen, significant halothane-induced malondialdehyde formation was found. This evidence supports the hypothesis that halothane can induce lipid peroxidation. The Po2 (i) must be low enough to permit the reductive formation of . CF3 CHCl-radicals but (ii), it must be high enough to promote formation of lipid peroxides.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Halothane / pharmacology*
  • In Vitro Techniques
  • Lipid Peroxides / metabolism*
  • Male
  • Malondialdehyde / metabolism
  • Microsomes, Liver / drug effects
  • Microsomes, Liver / metabolism*
  • NADP / pharmacology
  • Oxygen / pharmacology*
  • Partial Pressure
  • Rats

Substances

  • Lipid Peroxides
  • Malondialdehyde
  • NADP
  • Oxygen
  • Halothane