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与β-肾上腺素能受体占有率相比,普萘洛尔、阿替洛尔和比索洛尔对人体运动性心动过速的降低作用

Reduction of exercise tachycardia in man after propranolol, atenolol and bisoprolol in comparison to beta-adrenoceptor occupancy.

作者信息

Wellstein A, Palm D, Belz G G, Butzer R, Polsak R, Pett B

机构信息

Zentrum der Pharmakologie, J. W. Goethe-Universität, Frankfurt, F.R.G.

出版信息

Eur Heart J. 1987 Dec;8 Suppl M:3-8. doi: 10.1093/eurheartj/8.suppl_m.3.

Abstract

In a double blind, placebo controlled study, propranolol (240 mg), atenolol (200 mg) or bisoprolol (100 mg) were administered as a single oral dose to groups of 6 healthy male volunteers. Exercise tachycardia was monitored for 84 hours after administration of the drugs to monitor beta blockade in vivo. Plasma samples drawn in parallel with these effects were used to detect beta 1- or beta 2-adrenoceptor occupancy in two subtype selective in vitro receptor binding assays. Reduction of exercise tachycardia parallels beta 1-adrenoceptor occupancy. Furthermore, at comparable beta 1-adrenoceptor occupancy, less beta 2-adrenoceptor occupancy was observed after bisoprolol than after atenolol. The latter finding is in agreement with the two-fold higher beta 1/beta 2-selectivity ratio of bisoprolol (75-fold) versus atenolol (35-fold). It is concluded, that beta blockade observed via the reduction of exercise tachycardia can be delineated from the in vitro occupancy of beta 1-adrenoceptors by an antagonist present in plasma samples.

摘要

在一项双盲、安慰剂对照研究中,对每组6名健康男性志愿者单次口服给予普萘洛尔(240毫克)、阿替洛尔(200毫克)或比索洛尔(100毫克)。给药后84小时监测运动性心动过速,以监测体内β受体阻滞情况。与这些效应同时采集的血浆样本用于在两种亚型选择性体外受体结合试验中检测β1或β2肾上腺素能受体占有率。运动性心动过速的降低与β1肾上腺素能受体占有率平行。此外,在可比的β1肾上腺素能受体占有率下,比索洛尔后观察到的β2肾上腺素能受体占有率低于阿替洛尔后。后一发现与比索洛尔(75倍)对比阿替洛尔(35倍)的β1/β2选择性比值高两倍一致。得出结论,通过运动性心动过速降低所观察到的β受体阻滞可与血浆样本中存在的拮抗剂对β1肾上腺素能受体的体外占有率区分开来。

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