Alradi A O, Carruthers S G
Clin Pharmacol Ther. 1985 Nov;38(5):495-502. doi: 10.1038/clpt.1985.214.
Diurnal, day-to-day, intrasubject, and intersubject variability of responsiveness of dorsal hand veins to norepinephrine has been investigated in healthy young subjects through the use of a novel technique in which a linear variable differential transformer (LVDT) is placed directly over the vein. Under constant operating conditions, control vein diameter remained consistent. There is a log dose responsiveness to norepinephrine infused directly into the hand vein. There was little diurnal, day-to-day, or intrasubject variability in the dose of norepinephrine required to induce 50% constriction of hand vein diameter. The responsiveness to norepinephrine of different veins in either hand was also consistent. However, there was wide intersubject variability, apparently unrelated to age, gender, or other subject characteristics. We conclude that the LVDT method is reproducible and reliable and offers a relatively noninvasive means of assessing the effects of disease and drugs on the human dorsal hand vein in vivo. The LVDT technique has been applied to study the rate of onset, magnitude of effect, dose responsiveness, and duration of action of intravenous dihydroergotamine, 0.1, 0.2, and 0.4 mg, on human dorsal hand veins. Despite systemic intravenous administration, there was an average delay in maximum response of 30 minutes to 1 hour. Venoconstriction was incomplete, with a maximum reduction of approximately 50% of vein diameter after each of the larger doses. There was no significant difference between the effects produced by 0.2 or 0.4 mg, which persisted for 6 hours after dosing.
通过一种新技术,即在健康年轻受试者的手背上直接放置线性可变差动变压器(LVDT),研究了手背静脉对去甲肾上腺素反应性的昼夜、每日、个体内和个体间变异性。在恒定的操作条件下,对照静脉直径保持一致。对手背静脉直接注入去甲肾上腺素存在对数剂量反应性。在诱导手背静脉直径收缩50%所需的去甲肾上腺素剂量方面,昼夜、每日或个体内变异性很小。双手不同静脉对去甲肾上腺素的反应性也一致。然而,个体间存在很大的变异性,显然与年龄、性别或其他受试者特征无关。我们得出结论,LVDT方法具有可重复性和可靠性,并提供了一种相对非侵入性的手段来评估疾病和药物对人手背静脉的体内影响。LVDT技术已被应用于研究静脉注射0.1、0.2和0.4mg双氢麦角胺对人手背静脉的起效速度、效应大小、剂量反应性和作用持续时间。尽管进行了全身静脉给药,但最大反应平均延迟30分钟至1小时。静脉收缩不完全,较大剂量给药后静脉直径最大减少约50%。0.2mg和0.4mg产生的效应之间没有显著差异,给药后持续6小时。