Datta R K, Johnson E A, Stenger R J
Arch Int Pharmacodyn Ther. 1976 Oct;223(2):180-6.
Three hr after i.p. administration of a single dose of 30 mg/kg of morphine to male mice, an increase in specific activity of NADPH-cytochrome c reductase by about 10% and the content of cytochrome P-450 by about 14% of their liver microsomes was observed.Administration of 30 mg/kg of morphine, once daily,during 5 days, caused about 16% and 9% increases in specific activity of c reductase and the content of P-450 respectively. Administration of a single dose of morphine to male and female mice caused no sex-dependent differences in the specific activity of c reductase and the content of P-450. Repeated administration of morphine up to 100 mg/kg to male mice increased the specific activity of microsomal c reductase by about 70%. Repeated administration of morphine up to 55 mg/kg also increased the microsomal content of P-450 by about 22%, but with higher doses of morphine, the content of P-450 declined and finally dropped below control levels. The levels of c-reductase activity and P-450 content returned to normal levels about 2 weeks after termination of morphine administration.
给雄性小鼠腹腔注射单剂量30mg/kg吗啡3小时后,观察到其肝脏微粒体中NADPH-细胞色素c还原酶的比活性增加约10%,细胞色素P-450含量增加约14%。每天一次给予30mg/kg吗啡,持续5天,分别使c还原酶的比活性和P-450含量增加约16%和9%。给雄性和雌性小鼠注射单剂量吗啡,在c还原酶的比活性和P-450含量上未引起性别依赖性差异。对雄性小鼠重复给予高达100mg/kg的吗啡,使微粒体c还原酶的比活性增加约70%。重复给予高达55mg/kg的吗啡也使微粒体P-450含量增加约22%,但吗啡剂量更高时,P-450含量下降,最终降至对照水平以下。停止给予吗啡约2周后,c还原酶活性和P-450含量水平恢复到正常水平。