Barthel W, Grossmann K
Int J Clin Pharmacol Ther Toxicol. 1982 Oct;20(10):458-64.
The venoconstrictor effect of dihydroergotamine and dihydroergotoxine was compared in ten volunteers and in tne patients suffering from varicosis of the leg veins. The dihydrogenated ergot alkaloids were administered subcutaneously in a dose of 0.5 mg each. The influence on the capacitance reaction was determined by occlusion plethysmography of the calf. In addition, the arterial resistance was measured in the same region. Dihydroergotamine reduces the capacitance reaction in volunteers only at the high occlusion pressure levels 8.0 and 10.7 kPa after a lag of 40 min, whereas dihydroergotoxine does not show any significant influence. On the other hand, dihydroergotamine and dihydroergotoxine lead to a significant decrease in capacitance reaction in the patients after 20 and 60 min, respectively. However, the effect if dihydroergotamine (2.1 ml/100 ml tissue) is significantly greater than that of dihydroergotoxine (1.2 ml/100 ml tissue) and nearly normalizes the increased capacitance reaction. The two drugs increase the arterial resistance more clearly in the volunteers than in the patients, and dihydroergotoxine more often than dihydroergotamine tends to decrease resistance when the pre-existent resistance value is low.
在10名志愿者和患有下肢静脉曲张的患者中比较了双氢麦角胺和双氢麦角毒碱的静脉收缩作用。将双氢麦角生物碱以每剂0.5毫克的剂量皮下给药。通过小腿的阻断体积描记法测定对容量反应的影响。此外,在同一区域测量动脉阻力。双氢麦角胺仅在40分钟的延迟后,在8.0和10.7千帕的高阻断压力水平下才会降低志愿者的容量反应,而双氢麦角毒碱则没有显示出任何显著影响。另一方面,双氢麦角胺和双氢麦角毒碱分别在20分钟和60分钟后导致患者的容量反应显著降低。然而,双氢麦角胺的作用(2.1毫升/100毫升组织)明显大于双氢麦角毒碱的作用(1.2毫升/100毫升组织),并且几乎使增加的容量反应正常化。这两种药物在志愿者中比在患者中更明显地增加动脉阻力,并且当预先存在的阻力值较低时,双氢麦角毒碱比双氢麦角胺更倾向于降低阻力。