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β-肾上腺素能受体阻断与内在拟交感活性——在缺血性心脏病治疗中的相关性

Beta-adrenoceptor blockade and intrinsic sympathomimetic activity--relevance in the treatment of ischaemic heart disease.

作者信息

Northcote R J, Ballantyne D

出版信息

Scott Med J. 1985 Oct;30(4):208-15. doi: 10.1177/003693308503000404.

Abstract

Beta adrenoceptor blockade has become one of the major therapeutic interventions in the medical management of ischaemic heart disease over the last 15 years. A number of beta adrenoceptor blockers have been developed with differing pharmacological properties including cardioselectivity and intrinsic sympathomimetic activity (ISA). The relevance of this latter property has been in some doubt. A number of reports suggest that ISA confers haemodynamic benefits although there does not appear to be any clear therapeutic advantage. In addition it would appear that patients with severe or rest angina might benefit more from a pure beta antagonist rather than one with ISA when the beta blocker is used as monotherapy, but this situation rarely arises. This paper reviews and assesses the value of treatment of ischaemic heart disease with beta blockers possessing intrinsic sympathomimetic activity.

摘要

在过去15年中,β肾上腺素能受体阻滞剂已成为缺血性心脏病药物治疗的主要干预措施之一。已经开发出多种具有不同药理特性的β肾上腺素能受体阻滞剂,包括心脏选择性和内在拟交感活性(ISA)。后一种特性的相关性一直存在一些疑问。一些报告表明,ISA具有血流动力学益处,尽管似乎没有任何明显的治疗优势。此外,当β受体阻滞剂作为单一疗法使用时,重度或静息性心绞痛患者似乎可能从纯β拮抗剂而非具有ISA的药物中获益更多,但这种情况很少出现。本文综述并评估了具有内在拟交感活性的β受体阻滞剂治疗缺血性心脏病的价值。

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