Kobylińska K, Pachecka J
Department of Biochemistry and Clinical Chemistry, Faculty of Pharmacy, Medical University of Warsaw, Poland.
Acta Pol Pharm. 1997 Nov-Dec;54(6):443-5.
The effects of phenobarbital (PB), carbamazepine (CBZ) and diazepam (DZ) on total hepatic cytochrome P450, cytochromes P4502B1/2B2 contents and aminopyrine N-demethylase activity was investigated. Adult male rats were treated per os with PB (80 mg/kg/day), CBZ (75 mg/kg/day) or DZ (90 mg/kg/day) for 3 consecutives days. Carbamazepine and phenobarbital produced significant increase of the contents of total cytochrome P450 and cytochromes P4502B1/2B2 as well as aminopyrine N-demethylase activity. In contrast, diazepam decreased the total hepatic cytochrome P450 content. This drug did not affect the level of cytochromes P4502B1/2B2 but increased aminopyrine N-demethylase activity comparing to the control animals.
研究了苯巴比妥(PB)、卡马西平(CBZ)和地西泮(DZ)对肝脏总细胞色素P450、细胞色素P4502B1/2B2含量及氨基比林N-脱甲基酶活性的影响。成年雄性大鼠连续3天经口给予PB(80毫克/千克/天)、CBZ(75毫克/千克/天)或DZ(90毫克/千克/天)。卡马西平和苯巴比妥使总细胞色素P450、细胞色素P4502B1/2B2含量以及氨基比林N-脱甲基酶活性显著增加。相比之下,地西泮降低了肝脏总细胞色素P450含量。与对照动物相比,该药物不影响细胞色素P4502B1/2B2水平,但增加了氨基比林N-脱甲基酶活性。