Literature DB >> 7647901

The ratio of reduced glutathione/oxidized glutathione is maintained in the liver during short-term hepatic hypoxia.

R Denno1, A Takabayashi, M Sugano, M Awane, M B Jin, T Morimoto, K Tanaka, Y Yamaoka, N Kobayashi, K Ozawa.   

Abstract

Controversy persists as to whether reperfusion-induced injuries actually occur in the hepatocyte. The liver is the major source of glutathione, a scavenger of hydrogen peroxide. The aim of this study was to evaluate the sensitivity of the ratio of reduced glutathione (GSH) to oxidized glutathione (GSSG) [GSH:GSSG] as an index of hepatic metabolic stress. A total of 121 rats were studied. The superior mesenteric vein (SMV) was occluded for 30 min, and this was followed by 0, 10, or 120 min of reperfusion. Total glutathione and GSSG levels in the liver, bile, and plasma were quantified, using glutathione reductase-coupled enzymatic assays. Results indicated that the hepatic GSH/GSSG ratio was maintained after an occlusion of the SMV, despite a decrease in adenosine triphosphate (ATP) level and energy charge potential. However, plasma levels of total glutathione and GSSG in the inferior vena cava increased after SMV occlusion and continued to increase after reperfusion. Biliary GSSG efflux decreased during 30-min occlusion of the SMV, and remained low even after reperfusion. The liver maintains homeostasis despite a decrease in biliary GSSG efflux, probably by secreting excess GSSG into the hepatic vein when the SMV is occluded. We conclude that the total amount of glutathione and GSSG in the plasma is directly correlated with oxidative stress in the liver.

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Year:  1995        PMID: 7647901     DOI: 10.1007/bf02347509

Source DB:  PubMed          Journal:  J Gastroenterol        ISSN: 0944-1174            Impact factor:   7.527


  24 in total

1.  Oxidation in the NADP system and release of GSSG from hemoglobin-free perfused rat liver during peroxidatic oxidation of glutathione by hydroperoxides.

Authors:  H Sies; C Gerstenecker; H Menzel; L Flohé
Journal:  FEBS Lett       Date:  1972-10-15       Impact factor: 4.124

2.  Reactive oxygen species during ischemia-reflow injury in isolated perfused rat liver.

Authors:  H Jaeschke; C V Smith; J R Mitchell
Journal:  J Clin Invest       Date:  1988-04       Impact factor: 14.808

3.  Oxygen free radicals and glutathione in hepatic ischemia/reperfusion injury.

Authors:  H J Stein; M M Oosthuizen; R A Hinder; H Lamprechts
Journal:  J Surg Res       Date:  1991-04       Impact factor: 2.192

4.  Exchange of cystine and glutamate across plasma membrane of human fibroblasts.

Authors:  S Bannai
Journal:  J Biol Chem       Date:  1986-02-15       Impact factor: 5.157

5.  Biliary transport of glutathione disulfide studied with isolated rat-liver canalicular-membrane vesicles.

Authors:  T Akerboom; M Inoue; H Sies; R Kinne; I M Arias
Journal:  Eur J Biochem       Date:  1984-05-15

6.  Glutathione disulfide as index of oxidant stress in rat liver during hypoxia.

Authors:  H Jaeschke
Journal:  Am J Physiol       Date:  1990-04

7.  Arterial levels of oxidized glutathione (GSSG) reflect oxidant stress in vivo.

Authors:  E K Abdalla; M G Caty; K S Guice; D B Hinshaw; K T Oldham
Journal:  J Surg Res       Date:  1990-04       Impact factor: 2.192

8.  Changes in the levels of endogenous coenzyme Q homologs, alpha-tocopherol, and glutathione in rat liver after hepatic ischemia and reperfusion, and the effect of pretreatment with coenzyme Q10.

Authors:  S Marubayashi; K Dohi; K Yamada; T Kawasaki
Journal:  Biochim Biophys Acta       Date:  1984-01-24

9.  The mechanism of biliary secretion of reduced glutathione. Analysis of transport process in isolated rat-liver canalicular membrane vesicles.

Authors:  M Inoue; R Kinne; T Tran; I M Arias
Journal:  Eur J Biochem       Date:  1983-08-15

10.  Induction of cystine transport activity in mouse peritoneal macrophages.

Authors:  H Watanabe; S Bannai
Journal:  J Exp Med       Date:  1987-03-01       Impact factor: 14.307

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