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β-肾上腺素能受体阻滞剂的外周血管效应:两种药物的比较。

Peripheral vascular effects of beta-adrenoceptor blockade: comparison of two agents.

作者信息

Cooke E D, Maltz M B, Smith R E, Bowcock S A, Watkins C J, Camm A J

机构信息

Department of Medical Electronics and Physics, St Bartholomew's Hospital Medical College, London.

出版信息

Br J Clin Pharmacol. 1987 Sep;24(3):359-66. doi: 10.1111/j.1365-2125.1987.tb03181.x.

Abstract
  1. The effects of atenolol (100 mg), a beta 1-adrenoceptor blocker, and bevantolol (200 mg) were compared on heart rate, blood pressure, lung function and on the peripheral circulation in normal volunteers before and after isoprenaline infusion. Recordings were obtained 2 and 24 h following a single dose and 24 h after continuous dosage for 7 days. 2. The effect of atenolol on the blockade of beta-adrenergic stimuli, as measured by the ability to reduce isoprenaline-induced tachycardia, was greater than that of bevantolol. Though both drugs achieved a similar reduction in systolic pressure there was a significantly greater reduction in diastolic pressure with bevantolol. The lung function tests gave similar results to those with other beta-adrenoceptor blockers. 3. Atenolol produced a fall in peripheral blood flow consistent with unopposed peripheral alpha-adrenoceptor stimulation. The effect of bevantolol differs from that of atenolol, an initial fall in peripheral blood flow being followed by a rapid recovery to baseline or greater. This effect may be due to partial alpha-adrenoceptor agonist activity.
摘要
  1. 在正常志愿者中,比较了β1肾上腺素能受体阻滞剂阿替洛尔(100毫克)和贝凡洛尔(200毫克)在静脉输注异丙肾上腺素前后对心率、血压、肺功能和外周循环的影响。在单次给药后2小时和24小时以及连续给药7天后24小时进行记录。2. 以降低异丙肾上腺素诱发的心动过速的能力来衡量,阿替洛尔对β肾上腺素能刺激的阻断作用大于贝凡洛尔。尽管两种药物在收缩压降低方面相似,但贝凡洛尔在舒张压降低方面显著更大。肺功能测试结果与其他β肾上腺素能受体阻滞剂的结果相似。3. 阿替洛尔使外周血流量下降,这与外周α肾上腺素能受体无对抗性刺激一致。贝凡洛尔的作用与阿替洛尔不同,外周血流量最初下降,随后迅速恢复至基线或更高水平。这种作用可能归因于部分α肾上腺素能受体激动剂活性。

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本文引用的文献

1
Cardioselectivity studies.心脏选择性研究
Proc R Soc Med. 1977;70(Suppl 5):48-9. doi: 10.1177/00359157770700S520.
9
Clinical pharmacokinetics and metabolism of bevantolol.
Angiology. 1986 Mar;37(3 Pt 2):221-5. doi: 10.1177/000331978603700313.

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