Hinderling P H, Gundert-Remy U, Schmidlin O, Heinzel G
J Pharm Sci. 1985 Jul;74(7):711-7. doi: 10.1002/jps.2600740703.
This study determined the kinetics of the effects of atropine on heart rate and saliva flow in three healthy male volunteers after intravenous administration of 1.35 and 2.15 mg of the drug. The pharmacokinetics of atropine and its primary metabolite, tropine, were determined simultaneously. Both the pharmacokinetic and effect data were fitted to an integrated kinetic-dynamic model. The maximum heart rate and minimum saliva flow occurred with a significant delay of 7-8 min after drug administration. Both effects were nonlinearly related to the amount of drug in the peripheral compartment. Maximum heart rates of 192 and 217% of the control values were observed at the lower and higher dose levels, respectively. Minimum saliva flows of 8 and 3% of the control values were measured after the lower and higher doses of atropine, respectively. The time durations of the positive chronotropic effect of the drug were 170 and 250 min at the lower and higher dose levels, respectively; the corresponding values for the length of the antisialogogue effect of the drug were 230 and 340 min, respectively.
本研究测定了三名健康男性志愿者静脉注射1.35毫克和2.15毫克阿托品后,阿托品对心率和唾液分泌的影响动力学。同时测定了阿托品及其主要代谢产物托品的药代动力学。药代动力学和效应数据均拟合到一个综合的动力学-动态模型中。给药后7-8分钟出现显著延迟,达到最大心率和最小唾液分泌量。两种效应均与外周室中的药物量呈非线性关系。在较低和较高剂量水平下,分别观察到最大心率为对照值的192%和217%。较低和较高剂量的阿托品给药后,分别测得最小唾液分泌量为对照值的8%和3%。药物正性变时作用的持续时间在较低和较高剂量水平分别为170分钟和250分钟;药物抗唾液分泌作用持续时间的相应值分别为230分钟和340分钟。