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地尔硫䓬和维拉帕米:人体中外源性去甲肾上腺素和血管紧张素II的功能性拮抗作用。

Diltiazem and verapamil: functional antagonism of exogenous noradrenaline and angiotensin II in man.

作者信息

Magometschnigg D, Hörtnagl H, Rameis H

出版信息

Eur J Clin Pharmacol. 1984;26(3):303-7. doi: 10.1007/BF00548759.

Abstract

To evaluate the possible functional antagonism of the calcium antagonists diltiazem and verapamil of the sympathetic nervous system and the renin-angiotensin system, their influence on blood pressure, heart rate, plasma catecholamines and renin activity (PRA), and on the reaction of these parameters to exogenous noradrenaline (NA) and angiotensin II, was investigated in 8 normotensive volunteers. Intravenous diltiazem or verapamil caused a sharp, shortlasting decrease in systolic and diastolic blood pressure, with a maximum 1-3 min after injection and a duration of 10-15 min. Even a further infusion of the calcium antagonists was unable to maintain the initial hypotensive effect. The cessation of the hypotensive effect was not due to reflex stimulation of the sympathetic nervous system, as indicated by unchanged plasma NA and adrenaline levels in the case of diltiazem, but was associated with an increase in PRA. During the administration of diltiazem and verapamil, the increase in blood pressure in response to the infusion of NA and angiotensin II was attenuated; the increase in diastolic pressure was mainly affected. The inhibition was more pronounced at the higher infusion rate of NA and angiotensin II. On the basis of these findings it is suggest that the hypotensive activity of calcium antagonists can be at least partly attributed to a reduction in vascular tone which is maintained by the postjunctional action of noradrenaline and angiotensin II.

摘要

为评估钙拮抗剂地尔硫䓬和维拉帕米对交感神经系统及肾素 - 血管紧张素系统可能存在的功能拮抗作用,在8名血压正常的志愿者中研究了它们对血压、心率、血浆儿茶酚胺和肾素活性(PRA)的影响,以及对这些参数对外源性去甲肾上腺素(NA)和血管紧张素II反应的影响。静脉注射地尔硫䓬或维拉帕米可使收缩压和舒张压急剧、短暂下降,注射后1 - 3分钟降至最低,持续10 - 15分钟。即使进一步输注钙拮抗剂也无法维持最初的降压效果。降压效果的消失并非由于交感神经系统的反射性刺激,如地尔硫䓬给药时血浆NA和肾上腺素水平未变所表明的那样,而是与PRA升高有关。在给予地尔硫䓬和维拉帕米期间,对输注NA和血管紧张素II的血压升高反应减弱;舒张压升高主要受到影响。在NA和血管紧张素II较高输注速率时抑制作用更明显。基于这些发现,提示钙拮抗剂的降压活性至少部分可归因于血管张力的降低,而血管张力是由去甲肾上腺素和血管紧张素II的节后作用维持的。

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