Cheesman M J, Mason S R, Reilly P E
Department of Biochemistry, University of Queensland, Brisbane, Australia.
J Steroid Biochem Mol Biol. 1996 Jul;58(4):447-54. doi: 10.1016/0960-0760(96)00063-5.
We have studied the effects of food deprivation and adrenalectomy on the induction by RU486 of female rat liver microsomal CYP3A apoprotein, erythromycin N-demethylase and diazepam C3-hydroxylase activities. RU486 was a potent inducer of CYP3A apoprotein in intact animals and food deprivation enhanced this response. Food deprivation alone caused only weak CYP3A apoprotein induction suggesting a synergistic interaction in the regulation of protein expression. These results were reflected in the measurements of diazepam C3-hydroxylase activity. This confirms diazepam C3-hydroxylase as a useful and easily measured index of CYP3A monooxygenase content in female rat liver microsomes. Erythromycin N-demethylase did not show concordance with this pattern; this monooxygenase was much more strongly induced by food deprivation alone than by RU486 administration and, in addition, adrenalectomy abolished the induction response to food deprivation. The lack of correspondence between the apoprotein and erythromycin N-demethylase results suggests that non-CYP3A or novel, hitherto uncharacterized CYP3A isoforms may contribute to erythromycin N-demethylation in female rats. The close agreement between the results for CYP3A apoprotein and diazepam C3-hydroxylase indicates that although RU486 possesses a terminal acetylenic moeity it does not, at the dosages used here, cause mechanism-based inactivation of the CYP3A monooxygenase protein it induces. Current studies are directed to characterizing the particular CYP3A isoform(s) whose production is stimulated by RU486.
我们研究了饥饿和肾上腺切除对RU486诱导雌性大鼠肝微粒体CYP3A载脂蛋白、红霉素N-脱甲基酶和地西泮C3-羟化酶活性的影响。在完整动物中,RU486是CYP3A载脂蛋白的强效诱导剂,饥饿增强了这种反应。单独饥饿仅引起微弱的CYP3A载脂蛋白诱导,提示在蛋白质表达调节中存在协同相互作用。这些结果在地西泮C3-羟化酶活性的测定中得到体现。这证实地西泮C3-羟化酶是雌性大鼠肝微粒体中CYP3A单加氧酶含量的一个有用且易于测量的指标。红霉素N-脱甲基酶未表现出与此模式一致;这种单加氧酶单独饥饿诱导的程度比给予RU486时更强,此外,肾上腺切除消除了对饥饿的诱导反应。载脂蛋白和红霉素N-脱甲基酶结果缺乏对应性表明,非CYP3A或新的、迄今未鉴定的CYP3A同工型可能参与雌性大鼠中红霉素的N-脱甲基化。CYP3A载脂蛋白和地西泮C3-羟化酶的结果密切一致,表明尽管RU486具有末端乙炔基,但在此处使用的剂量下,它不会导致其诱导的CYP3A单加氧酶蛋白发生基于机制的失活。目前的研究旨在鉴定受RU486刺激产生的特定CYP3A同工型。