Fischer E, Gregus Z
Arch Int Pharmacodyn Ther. 1980 Oct;247(2):190-7.
The time-course effect of a single dose (75 mg/kg i.p.) of phenobarbital (PB) and that of prolonged PB treatment (75 mg/kg daily i.p., for 1 to 5 days) on the hepatic excretory and microsomal enzyme functions have been studied in rats. PB given in a single dose resulted in hypercholeresis 6 hr, an increase in the biliary excretion rate of bromcresol green and in hepatic cytochrome P-45 concentration 12 hr, and shortening of hexobarbital sleeping time 24 hr after the administration. All these changes, except the hypercholeresis, became gradually more apparent following the repeated daily administration of PB. Regression of the changes was faster in biliary excretory function than in microsomal function. Biliary flow and biliary output of bromcresol green returned to the control level at 72 hr after a single dose of PB or at 5 days after the cessation of a 5-day PB treatment, whereas enzyme induction was still apparent at those times. These results indicate that no close correlation in time exists between PB produced hepatic microsomal enzyme induction and the stimulatory effect of PB on biliary excretion.
研究了单次腹腔注射苯巴比妥(PB,75mg/kg)以及长期PB治疗(每天腹腔注射75mg/kg,持续1至5天)对大鼠肝脏排泄和微粒体酶功能的时程效应。单次给药PB导致给药后6小时胆汁分泌增多,12小时溴甲酚绿胆汁排泄率增加以及肝细胞色素P - 45浓度升高,24小时己巴比妥睡眠时间缩短。除胆汁分泌增多外,所有这些变化在PB每日重复给药后逐渐变得更加明显。胆汁排泄功能变化的恢复比微粒体功能更快。单次注射PB后72小时或5天PB治疗停止后5天,胆汁流量和溴甲酚绿胆汁输出量恢复到对照水平,而此时酶诱导作用仍然明显。这些结果表明,PB产生的肝脏微粒体酶诱导与PB对胆汁排泄的刺激作用之间在时间上不存在密切相关性。