Suppr超能文献

阿替洛尔及其他一些β-肾上腺素受体阻断剂对去甲肾上腺素诱发的离体灌注大鼠心脏反应的影响。

Effects of atenolol and some other beta-adrenoceptor blocking agents on norepinephrine-induced responses in isolated and perfused rat hearts.

作者信息

Nakasone J, Kato T, Noguchi K, Nagamine F, Sakanashi M

机构信息

Department of Pharmacology, School of Medicine, Faculty of Medicine, University of the Ryukyus, Okinawa, Japan.

出版信息

Jpn J Pharmacol. 1988 Aug;47(4):387-95. doi: 10.1254/jjp.47.387.

Abstract

The effects of atenolol and another three beta-adrenoceptor blocking agents on norepinephrine (NE)-induced cardiac responses were examined in isolated and perfused rat hearts following a Langendorff method. Bolus injection of atenolol did not show significant inhibitory effects on NE-induced increases in myocardial contractile force (MCF) and heart rate. Bolus injections of metoprolol and timolol were also ineffective for inhibiting NE-responses. However, both bolus injection and infusion of propranolol or infusion of atenolol, metoprolol and timolol all significantly inhibited NE-responses. On sustained increase in MCF induced by infusion of NE, the inhibitory effect of atenolol was transient, while that of propranolol was continuous. From these results, it is concluded that atenolol displays a different time course of action on NE-induced cardiac responses by bolus injection or infusion because of its pharmacological properties, which may be due to its low lipophilicity.

摘要

采用Langendorff方法,在离体灌注大鼠心脏中研究了阿替洛尔和其他三种β-肾上腺素能受体阻滞剂对去甲肾上腺素(NE)诱导的心脏反应的影响。静脉注射阿替洛尔对NE诱导的心肌收缩力(MCF)增加和心率增加未显示出明显的抑制作用。静脉注射美托洛尔和噻吗洛尔对抑制NE反应也无效。然而,静脉注射和输注普萘洛尔或输注阿替洛尔、美托洛尔和噻吗洛尔均显著抑制NE反应。在由NE输注引起的MCF持续增加时,阿替洛尔的抑制作用是短暂的,而普萘洛尔的抑制作用是持续的。从这些结果可以得出结论,由于阿替洛尔的药理特性,其对静脉注射或输注NE诱导的心脏反应表现出不同的作用时间过程,这可能是由于其低亲脂性所致。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验