de Marées H, Welzel D, de Marées A, Klotz U, Tiedjen K U, Knaup G
Eur J Clin Pharmacol. 1986;30(6):685-9. doi: 10.1007/BF00608216.
In a double-blind, interindividual comparative study 30 healthy volunteers were randomly allocated to oral treatment with 5 or 10 mg of dihydroergotamine (DHE) or placebo once daily for 16 days. Regional basic venous blood volume (BBV), pressure dependent venous capacitance (CV) of the calf, resting heart rate and blood pressure were determined on Days 1 and 15 of treatment. Plasma concentrations of DHE were monitored on Days 2 and 16. Due to spontaneous vasodilation BBV varied considerably, showing that it is an inappropriate parameter for investigating the venoconstrictor activity of DHE. CV remained unchanged after the first dose of DHE but it had declined significantly on both dosage regimens at the end of the treatment phase. In contrast, the blood concentration profiles of DHE were comparable at the beginning and the end of the trial. The discrepancy can best be explained by the existence of an effect compartment, e.g. smooth vascular musculature, which slowly becomes filled with DHE and/or its active metabolites. The venoconstrictor activity of DHE exhibited a significant dose-response relationship.
在一项双盲、个体间比较研究中,30名健康志愿者被随机分配,每天口服5毫克或10毫克双氢麦角胺(DHE)或安慰剂,共16天。在治疗的第1天和第15天测定局部基础静脉血容量(BBV)、小腿压力依赖性静脉容量(CV)、静息心率和血压。在第2天和第16天监测DHE的血浆浓度。由于自发性血管舒张,BBV变化很大,表明它不是研究DHE静脉收缩活性的合适参数。首次给予DHE后CV保持不变,但在治疗阶段结束时,两种剂量方案下CV均显著下降。相比之下,试验开始和结束时DHE的血药浓度曲线具有可比性。这种差异最好用存在一个效应室来解释,例如血管平滑肌,它会慢慢被DHE和/或其活性代谢产物填满。DHE的静脉收缩活性呈现出显著的剂量反应关系。