Mitochondria and xanthine oxidase both generate reactive oxygen species in isolated perfused rat liver after hypoxic injury
Authors:
- Jerry R. MitchellJMJerry R. Mitchell
- 1 April 1989
- journal article
- research article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 160 (1) , 140-147
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Reoxygenation injury in isolated hepatocytes: Cell death precedes conversion of xanthine dehydrogenase to xanthine oxidaseBiochemical and Biophysical Research Communications, 1988
- Oxidant stress during reperfusion of ischemic liver: No evidence for a role of xanthine oxidaseHepatology, 1988
- Reactive oxygen species during ischemia-reflow injury in isolated perfused rat liver.Journal of Clinical Investigation, 1988
- Hypoxic damage generates reactive oxygen species in isolated perfused rat liverBiochemical and Biophysical Research Communications, 1988
- LEVELS OF PURINE COMPOUNDS IN A PERFUSATE AS A BIOCHEMICAL MARKER OF ISCHEMIC INJURY OF COLD-PRESERVED LIVER1Transplantation, 1987
- INFLUENCE OF OXYGEN-DERIVED FREE RADICAL SCAVENGERS ON ISCHEMIC LIVERSTransplantation, 1985
- Oxygen-Derived Free Radicals in Postischemic Tissue InjuryNew England Journal of Medicine, 1985
- Bile Secretion in Hemoglobin-Free Perfused Rat LiverHoppe-Seyler´s Zeitschrift Für Physiologische Chemie, 1984
- Biliary excretion of glutathione and glutathione disulfide in the rat. Regulation and response to oxidative stress.Journal of Clinical Investigation, 1984
- Oxidation in the NADP system and release of GSSG from hemoglobin‐free perfused rat liver during peroxidatic oxidation of glutathione by hydroperoxidesFEBS Letters, 1972