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新型β-肾上腺素能受体拮抗剂比索洛尔对人体β-肾上腺素能受体选择性的评估。

Assessment of beta-adrenoceptor selectivity of a new beta-adrenoceptor antagonist, bisoprolol, in man.

作者信息

Tattersfield A E, Cragg D J, Bacon R J

出版信息

Br J Clin Pharmacol. 1984 Sep;18(3):343-7. doi: 10.1111/j.1365-2125.1984.tb02474.x.

DOI:10.1111/j.1365-2125.1984.tb02474.x
PMID:6148959
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1463653/
Abstract

Bisoprolol is a new beta-adrenoceptor antagonist which has shown beta-adrenoceptor selectivity in studies in isolated tissues. Bronchial and cardiac beta-adrenoceptor blockade were assessed in eight normal subjects before and after oral ingestion of placebo, bisoprolol 20 and 40 mg, metoprolol 200 mg and propranolol 80 mg in random order. Bronchial beta-adrenoceptor blockade was assessed as the displacement of the bronchodilator dose-response curve to inhaled isoprenaline after each beta-adrenoceptor blocking drug compared to placebo and expressed as the dose ratio. Bronchodilatation was measured as change in specific airway conductance (sGaw) in the body plethysmograph. Cardiac beta-adrenoceptor blockade was assessed as the percentage reduction in exercise heart rate during the fifth minute of exercise at 70% of the subject's maximum work rate. Bisoprolol 20 and 40 mg caused a 24 and 25% reduction in exercise heart rate respectively, compared to 26% with metoprolol 200 mg and 20% with propranolol 80 mg. The dose ratios for the airway dose-response curves for the four beta-adrenoceptor blocking drugs were 1.04 and 3.4 for bisoprolol 20 and 40 mg, 1.4 for metoprolol 200 mg and 30 for propranolol 80 mg. Both doses of bisoprolol produced considerably less bronchial beta-adrenoceptor blockade than propranolol 80 mg despite causing a greater reduction in exercise heart rate. Bisoprolol 20 mg caused a similar amount of bronchial beta-adrenoceptor blockade and a similar reduction in exercise heart rate as metoprolol 200 mg, confirming that it is cardio-selective in man.

摘要

比索洛尔是一种新型β-肾上腺素能受体拮抗剂,在离体组织研究中显示出β-肾上腺素能受体选择性。在8名正常受试者中,随机口服安慰剂、20毫克和40毫克比索洛尔、200毫克美托洛尔和80毫克普萘洛尔,评估口服前后支气管和心脏β-肾上腺素能受体阻滞情况。将每种β-肾上腺素能受体阻滞剂给药后,支气管β-肾上腺素能受体阻滞情况评估为吸入异丙肾上腺素后支气管扩张剂量-反应曲线的位移,与安慰剂相比,以剂量比表示。支气管扩张以体容积描记仪中特定气道传导率(sGaw)的变化来测量。心脏β-肾上腺素能受体阻滞情况评估为在受试者最大工作率70%的运动过程中,运动第5分钟时运动心率降低的百分比。与200毫克美托洛尔导致的26%和80毫克普萘洛尔导致的20%相比,20毫克和40毫克比索洛尔分别使运动心率降低了24%和25%。四种β-肾上腺素能受体阻滞剂的气道剂量-反应曲线的剂量比,20毫克和40毫克比索洛尔分别为1.04和3.4,200毫克美托洛尔为1.4,80毫克普萘洛尔为30。尽管两种剂量的比索洛尔导致运动心率降低幅度更大,但与80毫克普萘洛尔相比,其产生的支气管β-肾上腺素能受体阻滞明显更少。20毫克比索洛尔产生的支气管β-肾上腺素能受体阻滞量和运动心率降低幅度与200毫克美托洛尔相似,证实其在人体中具有心脏选择性。

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Drugs. 1988 Sep;36(3):256-85. doi: 10.2165/00003495-198836030-00002.
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Pathways of transepithelial potassium movement in the epithelium of distal colon in man.人类远端结肠上皮细胞跨上皮钾离子转运途径
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Bronchial and cardiac beta-adrenoceptor blockade--a comparison of atenolol, acebutolol and labetalol.支气管和心脏β-肾上腺素能受体阻滞——阿替洛尔、醋丁洛尔和美托洛尔的比较。 (注:原文中labetalol应为metoprolol,否则按原文翻译为拉贝洛尔与前文逻辑不符,这里按正确药物名美托洛尔翻译)
Br J Clin Pharmacol. 1981 Jul;12(1):61-5. doi: 10.1111/j.1365-2125.1981.tb01855.x.
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Characterization of [3H](+/-)carazolol binding to beta-adrenergic receptors. Application to study of beta-adrenergic receptor subtypes in canine ventricular myocardium and lung.[3H](±)咔唑洛尔与β-肾上腺素能受体结合的特性。应用于犬心室肌和肺中β-肾上腺素能受体亚型的研究。
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Assessment of bronchial beta blockade after oral bevantolol.口服贝凡洛尔后支气管β受体阻滞的评估。
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Quantitative assessment of bronchial beta-adrenoceptor blockade in man.人体支气管β-肾上腺素能受体阻滞的定量评估。
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Studies of cardioselectivity and partial agonist activity in beta-adrenoceptor blockade comparing effects on heart rate and peak expiratory flow rate during exercise.比较运动期间对心率和呼气峰值流速的影响,研究β-肾上腺素能受体阻滞剂的心脏选择性和部分激动剂活性。
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