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β-肾上腺素能受体拮抗剂的抗心绞痛作用。

Antianginal actions of beta-adrenoceptor antagonists.

作者信息

O'Rourke Stephen T

机构信息

Department of Pharmaceutical Sciences, College of Pharmacy, North Dakota State University, Fargo, ND 58105, USA.

出版信息

Am J Pharm Educ. 2007 Oct 15;71(5):95. doi: 10.5688/aj710595.

Abstract

Angina pectoris is usually the first clinical sign of underlying myocardial ischemia, which results from an imbalance between oxygen supply and oxygen demand in the heart. This report describes the pharmacology of beta-adrenoceptor antagonists as it relates to the treatment of angina. The beta-adrenoceptor antagonists are widely used in long-term maintenance therapy to prevent acute ischemic episodes in patients with chronic stable angina. Beta-adrenoceptor antagonists competitively inhibit the binding of endogenous catecholamines to beta1-adrenoceptors in the heart. Their anti-ischemic effects are due primarily to a reduction in myocardial oxygen demand. By decreasing heart rate, myocardial contractility and afterload, beta-adrenoceptor antagonists reduce myocardial workload and oxygen consumption at rest as well as during periods of exertion or stress. Predictable adverse effects include bradycardia and cardiac depression, both of which are a direct result of the blockade of cardiac beta1-adrenoceptors, but adverse effects related to the central nervous system (eg, lethargy, sleep disturbances, and depression) may also be bothersome to some patients. Beta-adrenoceptor antagonists must be used cautiously in patients with diabetes mellitus, peripheral vascular disease, heart failure, and asthma or other obstructive airway diseases. Beta-adrenoceptor antagonists may be used in combination with nitrates or calcium channel blockers, which takes advantage of the diverse mechanisms of action of drugs from each pharmacologic category. Moreover, concurrent use of beta-adrenoceptor antagonists may alleviate the reflex tachycardia that sometimes occurs with other antianginal agents.

摘要

心绞痛通常是潜在心肌缺血的首个临床症状,心肌缺血是由心脏氧供与氧需失衡所致。本报告描述了β肾上腺素能受体拮抗剂与心绞痛治疗相关的药理学特性。β肾上腺素能受体拮抗剂广泛用于长期维持治疗,以预防慢性稳定型心绞痛患者的急性缺血发作。β肾上腺素能受体拮抗剂竞争性抑制内源性儿茶酚胺与心脏β1肾上腺素能受体的结合。其抗缺血作用主要归因于心肌需氧量的降低。通过降低心率、心肌收缩力和后负荷,β肾上腺素能受体拮抗剂可降低静息时以及运动或应激期间的心肌工作量和氧消耗。可预测的不良反应包括心动过缓和心脏抑制,这两者都是心脏β1肾上腺素能受体被阻断的直接结果,但与中枢神经系统相关的不良反应(如嗜睡、睡眠障碍和抑郁)对一些患者来说也可能令人困扰。糖尿病、外周血管疾病、心力衰竭以及哮喘或其他阻塞性气道疾病患者必须谨慎使用β肾上腺素能受体拮抗剂。β肾上腺素能受体拮抗剂可与硝酸盐或钙通道阻滞剂联合使用,这利用了每个药理学类别的药物不同的作用机制。此外,同时使用β肾上腺素能受体拮抗剂可减轻有时与其他抗心绞痛药物同时出现的反射性心动过速。

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