Literature DB >> 7414619

Influence of hypoxia on the hepatotoxic effects of carbon tetrachloride, paracetamol, allyl alcohol, bromobenzene and thioacetamide.

O Strubelt, H Breining.   

Abstract

Exposure of rats to a reduced oxygen tension (6% O2, 94% N2) for 6 h increased the serum enzyme and the histological lesions induced by carbon tetrachloride (CCl4). Hypoxia did not enhance the hepatotoxic response to paracetamol, allyl alcohol, bromobenzene or thioacetamide. No correlation was found between the changes in hepatotoxicity induced by hypoxia and those after treatment with ethanol. Hepatic hypoxia therefore was not the pathogenetic mechanism responsible for ethanol-induced enhancement of hepatotoxicity.

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Year:  1980        PMID: 7414619     DOI: 10.1016/0378-4274(80)90176-9

Source DB:  PubMed          Journal:  Toxicol Lett        ISSN: 0378-4274            Impact factor:   4.372


  4 in total

1.  Tetrachloromethane metabolism in vivo under normoxia and hypoxia. Biochemical and histopathological effects relative to alkane exhalation.

Authors:  H Dürk; C Klessen; H Frank
Journal:  Arch Toxicol       Date:  1987       Impact factor: 5.153

2.  Potentiation of carbon tetrachloride hepatotoxicity by hypoxia.

Authors:  Y Shibayama
Journal:  Br J Exp Pathol       Date:  1986-12

3.  16,16-Dimethyl PGE2 and fatty acids protect hepatocytes against CCl4-induced damage.

Authors:  M J Ruwart; N M Nichols; K Hedeen; B D Rush; J Stachura
Journal:  In Vitro Cell Dev Biol       Date:  1985-08

Review 4.  Toxic drug effects associated with oxygen metabolism: redox cycling and lipid peroxidation.

Authors:  H Kappus; H Sies
Journal:  Experientia       Date:  1981-12-15
  4 in total

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