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倍他米松对大鼠体内外联苯2-羟化作用的影响。

Effects of betamethasone on the in vitro and in vivo 2-hydroxylation of biphenyl in the rat.

作者信息

Miller M S, Huang M T, Williams G M, Jeffrey A M, Conney A H

出版信息

Drug Metab Dispos. 1983 Nov-Dec;11(6):556-61.

PMID:6140139
Abstract

The in vitro addition of betamethasone to rat liver microsomes caused a concentration-dependent stimulation of biphenyl 2-hydroxylation. At a 100 microM concentration of betamethasone, the formation of 2-hydroxybiphenyl was increased by approximately 4-fold in microsomes from 28-day-old rats and 10-fold in liver microsomes from 5-day-old rats. The steroid had little or no effect on the hydroxylation of biphenyl in the 3- or 4-position except at the highest concentration tested (1 mM), where a 20-30% inhibition was observed. The ip injection of 0.01 to 10 mumol of betamethasone to 5-day-old rats had little or no effect on the total body metabolism of 0.01 to 3.5 mumol of biphenyl-2-3H to 2-hydroxybiphenyl as measured by 3H2O formation. Although betamethasone had no effect on the 2-hydroxylation of biphenyl in the intact rat, this reaction was stimulated 4- to 9-fold by the addition of 100 microM betamethasone to hepatocyte monolayer cultures.

摘要

在大鼠肝微粒体中体外添加倍他米松会引起联苯2-羟基化的浓度依赖性刺激。在倍他米松浓度为100微摩尔时,28日龄大鼠微粒体中2-羟基联苯的形成增加了约4倍,5日龄大鼠肝微粒体中增加了10倍。除了在测试的最高浓度(1毫摩尔)下观察到20-30%的抑制作用外,该类固醇对联苯在3-或4-位的羟基化几乎没有影响。给5日龄大鼠腹腔注射0.01至10微摩尔倍他米松,对0.01至3.5微摩尔2-3H联苯转化为2-羟基联苯的全身代谢几乎没有影响,这是通过3H2O的形成来测量的。虽然倍他米松对完整大鼠中联苯的2-羟基化没有影响,但在肝细胞单层培养物中添加100微摩尔倍他米松可使该反应刺激4至9倍。

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