四氯化碳
肝损伤
化学
药理学
生物化学
医学
有机化学
作者
Fernando J. Corrales,A. Giménez,Luis Álvarez,Joan Caballería,Marı́a A. Pajares,Hernán Andreu,Albert Parés,José M. Mato,Joan Rodés
出处
期刊:Hepatology
[Wiley]
日期:1992-10-01
卷期号:16 (4): 1022-1027
被引量:160
标识
DOI:10.1002/hep.1840160427
摘要
Administration of carbon tetrachloride to rats resulted in induction of hepatic fibrosis and a 60% reduction of hepatic S-adenosylmethionine synthetase activity without producing any significant modification of hepatic levels of S-adenosylmethionine synthetase messenger RNA. The reduction of S-adenosylmethionine synthetase activity was corrected by treatment with S-adenosylmethionine (3 mg/kg/day, intramuscularly). Administration of carbon tetrachloride also produced a 45% depletion of liver glutathione (reduced form) that was corrected by S-adenosylmethionine treatment. After the rats received carbon tetrachloride, a 2.3-fold increase in liver collagen was observed; prolyl hydroxylase activity was 2.5 times greater than that seen in controls. These increases were attenuated in animals treated with carbon tetrachloride and S-adenosylmethionine. The attenuation by S-adenosylmethionine treatment of the fibrogenic effect of carbon tetrachloride was associated with a decrease in the number of rats in which cirrhosis developed.
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