Gough P A, Curry S H, Araujo O E, Robinson J D, Dallman J J
Br J Clin Pharmacol. 1982 Nov;14(5):739-42. doi: 10.1111/j.1365-2125.1982.tb04966.x.
In a double-blind crossover design, the effect of cimetidine on oral diazepam pharmacokinetics and an evaluation of cognitive function change was studied in seven healthy volunteers. Subjects randomly received placebo or cimetidine 300 mg orally every 6 h for a total of five doses prior to diazepam 10 mg. A significant increase in diazepam elimination half-life from (mean +/- s.e. mean) 66.9 +/- 21.4 to 89.6 +/- 22.5 h (P = 0.006) and area under the plasma concentration-time curve from 5.06 +/- 1.47 to 8.93 +/- 1.88 micrograms ml-1 h (P = 0.028) was observed indicating a probable cimetidine induced inhibition of diazepam hepatic metabolism. Digit symbol substitution and visual analogue scales were used to measure the effect of an alteration of diazepam kinetics on cognitive function. An enhancement of pharmacological effect as reflected in digit symbol substitution scores and visual analogue scale measurements was not observed.
在一项双盲交叉设计中,研究了西咪替丁对口服地西泮药代动力学的影响以及对认知功能变化的评估,研究对象为7名健康志愿者。在服用10mg地西泮之前,受试者随机接受安慰剂或每6小时口服300mg西咪替丁,共服用五剂。观察到地西泮消除半衰期从(均值±标准误)66.9±21.4小时显著增加至89.6±22.5小时(P = 0.006),血浆浓度-时间曲线下面积从5.06±1.47微克·毫升⁻¹·小时增加至8.93±1.88微克·毫升⁻¹·小时(P = 0.028),这表明西咪替丁可能抑制了地西泮的肝脏代谢。使用数字符号替换和视觉模拟量表来测量地西泮动力学改变对认知功能的影响。未观察到数字符号替换分数和视觉模拟量表测量结果所反映的药理作用增强。