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The Effect of Cirrhosis of the Liver on Microsomal Detoxications and Cytochrome P-450

机译:肝硬化对微粒体解毒和细胞色素P-450的影响

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摘要

Cirrhosis has been produced in rats by a combination of carbon tetrachloride (CCl4) and phenobarbitone administration. Hepatic microsomal cytochrome P-450 contents have been measured during the production of cirrhosis, and in established cirrhosis, after recovery from the acute effects of CCl4 has taken place. Cytochrome P-450 levels fall after CCl4 dosage but recover rapidly to near normal values in the early stages of the regime although later on they remain at a low level. In rats given 8 weeks to recover from the acute effects of the cirrhosis-producing regime, P-450 and pyramidon demethylation levels remained depressed in the more severely cirrhotic animals. The response to the inducing effect of phenobarbitone was diminished also. Liver water remained high in the more severely cirrhotic rats, but was near normal in those with less severe lesions. The basis of the changes observed is discussed and the features of experimental cirrhosis and clinical cirrhosis in man are compared.
机译:四氯化碳(CCl4)和苯巴比妥联合给药可在大鼠中产生肝硬化。在肝硬化发生期间和已经建立的肝硬化中,从CCl4的急性作用中恢复后,已经测量了肝微粒体细胞色素P-450的含量。细胞色素P-450的水平在CCl4给药后下降,但在治疗初期可迅速恢复至接近正常值,尽管后期仍保持较低水平。在给予大鼠八周时间以使其从肝硬化发生方案的急性影响中恢复过来的情况下,在肝硬化较严重的动物中,P-450和锥体神经元去甲基化水平仍然较低。对苯巴比妥的诱导作用的反应也减少了。在肝硬化较严重的大鼠中,肝水仍然很高,但在病变较轻的大鼠中,肝水却接近正常。讨论了观察到的变化的基础,并比较了实验性肝硬化和男性临床肝硬化的特征。

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