Andros E, Detmar-Hanna D, Suteparuk S, Gal J, Gerber J G
Division of Clinical Pharmacology and Toxicology, University of Colorado Health Sciences Center, Denver 80262, USA.
Eur J Clin Pharmacol. 1996;50(1-2):41-6. doi: 10.1007/s002280050067.
The effect of age on the pharmacokinetics and pharmacodynamics of prazosin (alpha 1 adrenoceptor blocker) was studied in 20 healthy volunteers.
Ten elderly (61-81 y) and ten young (23-28 y) subjects were studied. All subjects received 1 mg of prazosin orally in a fasting state. Serial blood samples were collected for calculation of oral pharmacokinetics, and blood pressure and pulse rate were measured during blood collection. Subjects remained supine and fasting for the first three hours post drug administration, after which they were allowed to ambulate and eat.
The oral pharmacokinetics of prazosin were not different in the two age groups. The serum t1/2 in the elderly was 210 min while in the young group was 139 min. The AUC(zero)-infinity in the two groups was not different. The Cmax was identical in the two groups, and the time to Cmax was 84 min in the elderly and 114 min in the young subjects. Protein binding was 93.4% in the elderly and 93.5% in the young subjects and the serum alpha 1 acid glycoprotein concentration was not different in the two groups of subjects. Even though the pharmacokinetics of prazosin were unchanged by age, the haemodynamic effects of the drug were greater in the elderly. The fall in systolic blood pressure and mean blood pressure was significantly greater in the elderly group at multiple time points after drug administration while the change in diastolic blood pressure was equivalent in the two age groups. Despite a greater decrease in mean blood pressure in the elderly, the compensatory increase in heart rate was similar in the two age groups suggesting a difference in the baroreceptor reflex in the two age groups.
The results of this study demonstrate that age does not alter the pharmacokinetics of oral prazosin, but the pharmacodynamic response at equivalent plasma prazosin concentration is greater in the elderly.
在20名健康志愿者中研究年龄对哌唑嗪(α1肾上腺素能受体阻滞剂)药代动力学和药效动力学的影响。
研究了10名老年人(61 - 81岁)和10名年轻人(23 - 28岁)。所有受试者在禁食状态下口服1毫克哌唑嗪。采集系列血样以计算口服药代动力学,并在采血期间测量血压和脉搏率。给药后前3小时受试者保持仰卧和禁食状态,之后允许他们走动和进食。
两个年龄组中哌唑嗪的口服药代动力学无差异。老年人的血清t1/2为210分钟,而年轻组为139分钟。两组的AUC(零)-无穷大无差异。两组的Cmax相同,老年人达到Cmax的时间为84分钟,年轻人为114分钟。老年人的蛋白结合率为93.4%,年轻人为93.5%,两组受试者的血清α1酸性糖蛋白浓度无差异。尽管哌唑嗪的药代动力学不受年龄影响,但该药物对老年人的血流动力学效应更大。给药后多个时间点,老年组收缩压和平均血压的下降明显更大,而两个年龄组舒张压的变化相当。尽管老年人平均血压下降幅度更大,但两个年龄组心率的代偿性增加相似,提示两个年龄组压力感受器反射存在差异。
本研究结果表明,年龄不改变口服哌唑嗪的药代动力学,但在等效血浆哌唑嗪浓度下,老年人的药效动力学反应更大。