Choudhuri S, Zhang X J, Waskiewicz M J, Thomas P E
Laboratory for Cancer Research, Rutgers University, Piscataway, NJ 08855, USA.
J Biochem Toxicol. 1995 Dec;10(6):299-307. doi: 10.1002/jbt.2570100604.
Induction of P450 3A1 and P450 3A2 was studied in adult rat liver following treatment with a single high dose of dexamethasone (DEX). The increase of both P450 3A1 and 3A2 occurred at the level of mRNA as well as protein. P450 3A isozymes thus induced were catalytically active. No constitutive expression of P450 3A1 mRNA or protein was observed in males or females. Constitutive expression of P450 3A2 mRNA and protein was observed in males but not in females. Additionally, in females, P450 3A2 was almost nondetectable compared to that in males, at any dose of DEX. A time course study following DEX treatment showed that P450 3A1 mRNA and protein were detectable in both sexes at 12 hours, increased until 48 hours, and then declined. The decline was more rapid in males. P450 3A2 mRNA and protein increased as early as 3 hours, increased further up to 48 hours, and slowly declined thereafter. A dose-response study indicated that P450 3A1 mRNA and protein progressively increased in both sexes from a dose of 30 mg/kg. In contrast, P450 3A2 mRNA and protein in males did not increase up to a dose of 30 mg/kg but increased at higher doses. Total P450 content and P450 3A catalytic activity were also found to increase with time and dose.
用单次高剂量地塞米松(DEX)处理成年大鼠肝脏后,研究了细胞色素P450 3A1和P450 3A2的诱导情况。P450 3A1和3A2的增加在mRNA水平和蛋白质水平均有发生。如此诱导产生的P450 3A同工酶具有催化活性。在雄性和雌性大鼠中均未观察到P450 3A1 mRNA或蛋白质的组成型表达。在雄性大鼠中观察到了P450 3A2 mRNA和蛋白质的组成型表达,而在雌性大鼠中未观察到。此外,在雌性大鼠中,与雄性大鼠相比,无论DEX剂量如何,P450 3A2几乎检测不到。DEX处理后的时间进程研究表明,P450 3A1 mRNA和蛋白质在两性中12小时时均可检测到,持续增加至48小时,然后下降。雄性大鼠的下降更为迅速。P450 3A2 mRNA和蛋白质早在3小时时就开始增加,进一步增加至48小时,此后缓慢下降。剂量反应研究表明,从30 mg/kg的剂量开始,两性中P450 3A1 mRNA和蛋白质逐渐增加。相比之下,雄性大鼠中P450 3A2 mRNA和蛋白质在30 mg/kg的剂量下并未增加,但在更高剂量下增加。还发现总P450含量和P450 3A催化活性随时间和剂量增加。