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使用新型小动脉血管扩张剂MDL - 899对正常志愿者进行的药效学研究。

Pharmacodynamic studies in normal volunteers with MDL-899, a new arteriolar vasodilator.

作者信息

Howden C W, Elliott H L, Lawrie C B, Reid J L

出版信息

J Cardiovasc Pharmacol. 1983 Jul-Aug;5(4):552-6. doi: 10.1097/00005344-198307000-00007.

Abstract

We conducted pharmacodynamic studies with a new vasodilator, MDL-899. Following initial dose-ranging studies we studied eight male normotensive volunteers, each of whom received, orally, 10 mg MDL-899 or placebo in double-blind random order. MDL-899 significantly lowered standing blood pressure, the maximal effect occurring 3-6 h following drug administration. There was a significant increase in heart rate in both supine and standing positions, maximal 6-8 h postdose. Supine plasma noradrenaline concentrations were greater following MDL-899, with the greatest difference present 4 h after drug administration. Plasma renin concentrations were greater following MDL-899. Six of our subjects were also given 10 mg MDL-899 together with 100 mg atenolol, in an additional study. Atenolol increased the hypotensive effect and attenuated the tachycardia following MDL-899 alone. Side effects following MDL-899 administration included headache, lightheadedness, and tachycardia. These were reduced following atenolol coadministration. The haemodynamic profile of MDL-899 suggests that this drug acts as a direct arteriolar vasodilator in man. The observed increase in heart rate is likely mediated by reflex activation of the sympathetic nervous system.

摘要

我们使用一种新型血管扩张剂MDL - 899进行了药效学研究。在初步的剂量范围研究之后,我们对8名血压正常的男性志愿者进行了研究,他们每人都以双盲随机顺序口服10毫克MDL - 899或安慰剂。MDL - 899显著降低了站立位血压,最大效应出现在给药后3至6小时。仰卧位和站立位的心率均显著增加,最大变化出现在给药后6至8小时。服用MDL - 899后仰卧位血浆去甲肾上腺素浓度更高,给药后4小时差异最大。服用MDL - 899后血浆肾素浓度更高。在另一项研究中,我们的6名受试者还同时服用了10毫克MDL - 899和100毫克阿替洛尔。阿替洛尔增强了MDL - 899单独使用时的降压效果并减轻了心动过速。服用MDL - 899后的副作用包括头痛、头晕和心动过速。联合使用阿替洛尔后这些副作用有所减轻。MDL - 899的血流动力学特征表明,这种药物在人体中作为一种直接的小动脉血管扩张剂起作用。观察到的心率增加可能是由交感神经系统的反射性激活介导的。

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