7-Ethoxycoumarin metabolism in hepatocytes from pre- and postpubescent male rats.

L. B. Roochvarg, R. Thurman, F. Kauffman
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引用次数: 4

Abstract

Marked changes in rates of drug metabolism occur during adolescence; however, biochemical events underlying alterations in drug metabolism in whole hepatocytes during this period of development are not well established. Accordingly, metabolism of 7-ethoxycoumarin, a model substrate for mixed-function oxidation, was studied in hepatocytes isolated from prepubescent and postpubescent male rats. Rates of 7-ethoxycoumarin O-deethylation increased 2.4-fold from 65 to 154 pmol/10(6) cells/min in intact hepatocytes during the narrow period of adolescence. In contrast, microsomal 7-ethoxycoumarin O-deethylase was the same in preparations from the two groups of animals. 7-Hydroxycoumarin glucuronide production in hepatocytes increased 2-fold and sulfate formation increased 16-fold across puberty. The results indicate that increases in drug metabolism, particularly sulfate conjugation, are mediated by biochemical events in addition to increases in total amounts and specific activities of hepatic drug-metabolizing enzymes.
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雄性大鼠青春期前和青春期后肝细胞的乙氧香豆素代谢。
药物代谢率的显著变化发生在青春期;然而,在这一发育时期,整个肝细胞中药物代谢变化的生化事件尚未得到很好的证实。因此,我们研究了7-乙基香豆素(一种混合功能氧化的模型底物)在雄性大鼠的肝细胞中的代谢。在青少年时期,完整肝细胞中7-乙氧基香豆素o -去甲基化率从65 pmol/10(6)个细胞/分钟增加到154 pmol/10(6)个细胞/分钟,增加了2.4倍。相比之下,微粒体7-乙氧基香豆素o -去乙基酶在两组动物的制剂中是相同的。在青春期,肝细胞中7-羟基香豆素葡萄糖醛酸酯的产生增加了2倍,硫酸盐的形成增加了16倍。结果表明,除了肝脏药物代谢酶的总量和特定活性增加外,药物代谢的增加,特别是硫酸盐缀合作用的增加是由生化事件介导的。
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