Hoffman A, Levy G
Department of Pharmaceutics, School of Pharmacy State University of New York at Buffalo, Amherst 14260.
Pharm Res. 1989 Nov;6(11):976-81. doi: 10.1023/a:1015953715346.
There is considerable evidence of gender differences in the pharmacokinetics of numerous drugs, particularly in rodents, but very limited information concerning the effect of gender on pharmacodynamic characteristics (concentration-activity relationships). In this study, heptabarbital or phenobarbital was administered to male and female rats and the concentrations of these drugs in the brain, cerebrospinal fluid and serum at onset or offset of loss of righting reflex were determined. For heptabarbital, offset concentrations were determined in Lewis rats and onset concentrations in Wistar rats. Onset concentrations of phenobarbital were determined in Wistar rats. In all cases, the barbiturate concentrations in males were significantly lower than those in females at the pharmacologic endpoint. The biologic (serum) half-life of heptabarbital is much shorter in males (approximately 10 min) than in females (approximately 90 min) and this pharmacokinetic difference is reflected by the considerably longer duration of effect of the drug in females.
有大量证据表明,许多药物的药代动力学存在性别差异,尤其是在啮齿动物中,但关于性别对药效学特征(浓度-活性关系)影响的信息非常有限。在本研究中,给雄性和雌性大鼠施用庚巴比妥或苯巴比妥,并测定这些药物在翻正反射消失开始或结束时在脑、脑脊液和血清中的浓度。对于庚巴比妥,在Lewis大鼠中测定结束时的浓度,在Wistar大鼠中测定开始时的浓度。在Wistar大鼠中测定苯巴比妥开始时的浓度。在所有情况下,在药理学终点时,雄性大鼠体内巴比妥类药物的浓度显著低于雌性大鼠。庚巴比妥的生物(血清)半衰期在雄性大鼠中(约10分钟)比在雌性大鼠中(约90分钟)短得多,这种药代动力学差异反映在该药物在雌性大鼠中的作用持续时间长得多。