Kamimori G H, Smallridge R C, Redmond D P, Belenky G L, Fein H G
Department of Behavioral Biology, Walter Reed Army Institute of Research, Washington, DC.
Eur J Clin Pharmacol. 1990;39(4):395-7. doi: 10.1007/BF00315417.
Seven healthy males (19-32 y) underwent each of four separate conditions in a repeated measures design. Five of these subjects underwent an additional trial. In four of five trials subjects received 2.0 mg atropine sulfate intramuscularly in the anterolateral portion of the left thigh: at rest (T1); following completion of a single exercise (Ex) bout (T2), (Each bout consisted of 25 min of stationary cycling at 40% VO2 max with 5 min of seated rest), prior to three Ex bouts (T3) and following one and prior to three Ex bouts (T5). Trial 4 (T4) was the same as T3 with the substitution of a saline placebo. Serum samples were collected over a 12 h period and atropine concentration was determined by RIA. Ex trials were compared to T1. Ex prior to atropine (T2) significantly decreased the mean volume of distribution (Vz, 278 vs 232 l). Ex in T3 significantly decreased the serum half life (t1/2, 4.2 vs 3.5 h), Vz (278 vs 198 l), and clearance (CL, 763 vs 638 ml.min-1) and significantly increased the peak concentration (Cp, 6.7 vs 12.3 ng.ml-1) and area under the curve (AUC, 44.1 vs 53.1 ng.ml-1). In T5, Ex significantly decreased the t1/2 (3.4 h), Vz (182 l) and CL (575 ml.min-1) and significantly increased the absorption rate constant (ka, 0.482 vs 1.1 min-1), elimination rate constant (ke, 0.0012 vs 0.0015 min-1), Cp (14 ng.ml-1) and AUC (53.3 ng.h.ml-1). These results demonstrate that moderate Ex either prior to and/or immediately following drug administration has the capacity to significantly modify atropine pharmacokinetics.
7名健康男性(19 - 32岁)在重复测量设计中接受了4种不同的条件。其中5名受试者进行了额外的试验。在5次试验中的4次,受试者在左大腿前外侧肌肉注射2.0毫克硫酸阿托品:静息时(T1);单次运动(Ex)结束后(T2),(每次运动包括以40%最大摄氧量进行25分钟的固定自行车运动,随后5分钟坐位休息),在3次运动前(T3)以及在1次运动后和3次运动前(T5)。试验4(T4)与T3相同,但用生理盐水安慰剂替代。在12小时内采集血清样本,并通过放射免疫分析法测定阿托品浓度。将运动试验与T1进行比较。运动前注射阿托品(T2)显著降低了平均分布容积(Vz,278 vs 232升)。T3中的运动显著降低了血清半衰期(t1/2,4.2 vs 3.5小时)、Vz(278 vs 198升)和清除率(CL,763 vs 638毫升·分钟-1),并显著提高了峰值浓度(Cp,6.7 vs 12.3纳克·毫升-1)和曲线下面积(AUC,44.1 vs 53.1纳克·毫升-1)。在T5中,运动显著降低了t1/2(3.4小时)、Vz(182升)和CL(575毫升·分钟-1),并显著提高了吸收速率常数(ka,0.482 vs 1.1分钟-1)、消除速率常数(ke,0.0012 vs 0.0015分钟-1)、Cp(14纳克·毫升-1)和AUC(53.3纳克·小时·毫升-1)。这些结果表明,在给药前和/或给药后立即进行适度运动能够显著改变阿托品的药代动力学。