Literature DB >> 7295545

Studies on the mechanism of enhancement of carbon tetrachloride hepatotoxicity by Triton WR 1339.

E C de Ferreyra, E G de Toranzo, O M de Fenos, J A Castro.   

Abstract

Pretreatment of rats with Triton WR 1339 significantly enhanced the intensity of CC14-induced liver necrosis. Previous workers suggested that this effect might be due to enhancement by Triton WR 1339 of cellular degradative processes. This pretreatment, however, also enhanced the intensity of covalent binding of [14C]CC14 metabolites to microsomal protein at 3 or 6 h, but not 1 h after its administration. This effect is not due to changes of microsomal P-450 content or increased activity of mixed-function oxygenase-metabolizing drugs like pentobarbital. Pretreatment with Triton WR 1339 also partially increased CC14-induced peroxidation of microsomal lipids at 1, 3 or 6 h after administration of the hepatotoxin. Liver concentrations of CC14 in Triton WR 1339-treated rats were significantly higher at 3 or 6 h but not at 1, 10 or 24 after its i.p. administration. Triton WR 1339 treatment decreased the body temperature of the rats and further intensified the decrease produced by CC14. Results suggest that, in addition to possible effects of Triton WR 1339 administration on liver-cell degradative processes, there are other actions of this detergent on CC14 activation and lipid peroxidation which might play a role in the heightened response of the liver of CC14-induced injury.

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Year:  1981        PMID: 7295545      PMCID: PMC2041708     

Source DB:  PubMed          Journal:  Br J Exp Pathol        ISSN: 0007-1021


  19 in total

1.  SPINAL CORD TRANSECTION AND CCL-4-TOXICITY.

Authors:  R E LARSON; G L PLAA
Journal:  Experientia       Date:  1963-11-15

2.  A CORRELATION OF THE EFFECTS OF CERVICAL CORDOTOMY, HYPOTHERMIA AND CATECHOLAMINES ON CARBON TETRACHLORIDE-INDUCED HEPATIC NECROSIS.

Authors:  R E LARSON; G L PLAA
Journal:  J Pharmacol Exp Ther       Date:  1965-01       Impact factor: 4.030

3.  Antituberculous effect of certain surface-active polyoxyethylene ethers in mice.

Authors:  J W CORNFORTH; P D HART; R J W REES; J A STOCK
Journal:  Nature       Date:  1951-07-28       Impact factor: 49.962

4.  Comparison of the biochemical alterations elicited in livers from rats treated with carbon tetrachloride, chloroform, 1,1,2-trichloroethane and 1,1,1-trichloroethane.

Authors:  C D Klaassen; G L Plaa
Journal:  Biochem Pharmacol       Date:  1969-08       Impact factor: 5.858

5.  Studies on the irreversible binding of 14 C-CCl 4 to microsomal lipids in rats under varying experimental conditions.

Authors:  J A Castro; M I Gomez
Journal:  Toxicol Appl Pharmacol       Date:  1972-12       Impact factor: 4.219

Review 6.  Carbon tetrachloride hepatotoxicity.

Authors:  R O Recknagel
Journal:  Pharmacol Rev       Date:  1967-06       Impact factor: 25.468

7.  Prevention by cystamine of liver necrosis and early biochemical alterations induced by carbon tetrachloride.

Authors:  J A Castro; E V Cignoli; C R De Castro; O M De Fenos
Journal:  Biochem Pharmacol       Date:  1972-01       Impact factor: 5.858

8.  Lysosomal injury and hepatic necrosis. Effects of triton WR-1339 on liver cells in the rat.

Authors:  H Iturriaga; S Vaisman; M E Eugenia PINO; T Pereda
Journal:  Exp Mol Pathol       Date:  1971-06       Impact factor: 3.362

9.  Aggravation of hepatic necrosis by lysosomal injury.

Authors:  H Iturriaga; I Posalaki; E Rubin
Journal:  Exp Mol Pathol       Date:  1969-06       Impact factor: 3.362

10.  Liver parenchymal cell injury. IV. Pattern of incorporation of carbon and chlorine from carbon tetrachloride into chemical constituents of liver in vivo.

Authors:  E S Reynolds
Journal:  J Pharmacol Exp Ther       Date:  1967-01       Impact factor: 4.030

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