Lindner E, Beyhl F E
Experientia. 1978 Feb 15;34(2):226-7. doi: 10.1007/BF01944693.
Hexobarbital was given to anaesthetized mice for a period of 7 h by repeated i. p. injection, first of 100 mg/kg,then several times of 50 mg/kg. A high level of hexobarbital was maintained in the liver. The activity of microsomal drug-metabolizing enzymes was induced by this treatment with hexobarbital. 30 min after a single i. p. injection of 100 mg/kg of hexobarbital, there was a significant inhibition of aminopyrine N-demethylase but none of cytochrome c and neotetrazolium reductases. Hexobarbital in vitro inhibits aminopyrine N-demethylase but not cytochrome c reductase.
对麻醉小鼠通过腹腔内重复注射给予己巴比妥7小时,首次注射剂量为100mg/kg,随后几次注射剂量为50mg/kg。肝脏中维持着高水平的己巴比妥。这种己巴比妥治疗诱导了微粒体药物代谢酶的活性。在单次腹腔注射100mg/kg己巴比妥30分钟后,氨基比林N-脱甲基酶有显著抑制,但细胞色素c和新四氮唑还原酶无抑制。己巴比妥在体外抑制氨基比林N-脱甲基酶,但不抑制细胞色素c还原酶。