Source of oxygen free radicals produced by rat hepatocytes during postanoxic reoxygenation

Biochim Biophys Acta. 1995 Sep 21;1268(3):249-54. doi: 10.1016/0167-4889(95)00077-6.

Abstract

The aim of this study was to determine the cellular source of oxygen free radicals generated by isolated hepatocytes during post-anoxic reoxygenation. Superoxide anions (O2.-) were detected by lucigenin chemiluminescence. Cell damage was assessed by LDH release. During anoxia, the chemiluminescence decreased to background levels while LDH release increased 8-fold. During reoxygenation, O2.- formation increased 15-fold within 15 min then declined towards control levels. LDH release increased from 161 to 285 mU/min in the first 30 min of reoxygenation, then declined toward the control rate. Allopurinol, an inhibitor of the xanthine-xanthine oxidase system, did not inhibit O2.- formation nor LDH release. Antimycin, a mitochondrial complex III inhibitor that does not block O2.- formation, increased both O2.- generation and LDH release 82 and 133% respectively. Diphenyleneiodonium (DPI), a mitochondrial and microsomal NADPH oxidase inhibitor, reduced O2.- and LDH release 60-70%. SOD, which catalyzes the dismutation of O2.- to H2O2, was without effect on O2.- and LDH release, but TEMPO, a stable nitroxide which mimics SOD and easily penetrates the cell membrane, decreased O2.-86% without affecting LDH. These results suggest that mitochondria or microsomes are the principal sites of O2.- production during reoxygenation of isolated hepatocytes, whereas the cytosolic xanthine/xanthine oxidase system is apparently not involved.

Publication types

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

MeSH terms

  • Allopurinol / pharmacology
  • Animals
  • Antimycin A / pharmacology*
  • Cells, Cultured
  • Cyclic N-Oxides / pharmacology
  • Hypoxia / metabolism
  • L-Lactate Dehydrogenase / analysis
  • Liver / metabolism*
  • Male
  • Microsomes, Liver / metabolism
  • Mitochondria, Liver / metabolism
  • Oxygen / metabolism*
  • Rats
  • Rats, Sprague-Dawley
  • Superoxide Dismutase / pharmacology
  • Superoxides / metabolism*
  • Xanthine Oxidase / antagonists & inhibitors

Substances

  • Cyclic N-Oxides
  • Superoxides
  • Allopurinol
  • Antimycin A
  • L-Lactate Dehydrogenase
  • Superoxide Dismutase
  • Xanthine Oxidase
  • Oxygen
  • TEMPO