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β-2肾上腺素能受体对离体血液灌注犬心脏标本的窦性心率以及心房和心室收缩性的影响。

Beta-2 adrenoceptor-mediated effects on sinus rate and atrial and ventricular contractility on isolated, blood-perfused dog heart preparations.

作者信息

Akahane K, Furukawa Y, Ogiwara Y, Haniuda M, Chiba S

机构信息

Department of Pharmacology, Shinshu University School of Medicine, Matsumoto, Japan.

出版信息

J Pharmacol Exp Ther. 1989 Mar;248(3):1276-82.

PMID:2539461
Abstract

Changes in the sinus rate, right atrial contractile force and left ventricular contractile force in response to isoproterenol, epinephrine, dobutamine, salbutamol and procaterol were studied in isolated, blood-perfused right atrial or left ventricular cardiac preparations of the dog. Each substance elicited dose-dependent increases in the three parameters and the ranking of the potency (ED50) for each effect was isoproterenol greater than epinephrine greater than dobutamine greater than or equal to salbutamol greater than or equal to procaterol. The ED50 of procaterol for changing sinus rate was lower than for altering atrial and ventricular contractile force, whereas the ED50 of dobutamine for changing sinus rate was higher. Ranking on the basis of the ratio of increase in sinus rate to increase in atrial tension induced by the agonists gave the following order: procaterol greater than or equal to salbutamol greater than epinephrine greater than or equal to isoproterenol greater than dobutamine. Procaterol-induced increases in sinus rate and atrial contractile force were dose-dependently inhibited by the beta-2 adrenoceptor antagonist, ICI 118,551, but only attenuated slightly by the beta-1 antagonist, atenolol. On the other hand, the positive chrono- and inotropic effects on the right atrium induced by dobutamine and isoproterenol were blocked completely by atenolol. The epinephrine- or salbutamol-induced positive chrono- and inotropic responses in the right atrium were inhibited moderately by both antagonists, but ICI 118,551 inhibited sinus rate increases more effectively than the atrial tension increases.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在犬的离体、血液灌注右心房或左心室心脏标本中,研究了异丙肾上腺素、肾上腺素、多巴酚丁胺、沙丁胺醇和丙卡特罗对窦性心率、右心房收缩力和左心室收缩力的影响。每种物质均引起这三个参数呈剂量依赖性增加,每种效应的效价(ED50)排序为:异丙肾上腺素>肾上腺素>多巴酚丁胺≥沙丁胺醇≥丙卡特罗。丙卡特罗改变窦性心率的ED50低于改变心房和心室收缩力的ED50,而多巴酚丁胺改变窦性心率的ED50则较高。根据激动剂引起的窦性心率增加与心房张力增加的比值进行排序,结果如下:丙卡特罗≥沙丁胺醇>肾上腺素≥异丙肾上腺素>多巴酚丁胺。丙卡特罗引起的窦性心率和心房收缩力增加呈剂量依赖性地被β2肾上腺素能受体拮抗剂ICI 118,551抑制,但仅被β1拮抗剂阿替洛尔轻微减弱。另一方面,多巴酚丁胺和异丙肾上腺素对右心房的正性变时和变力作用被阿替洛尔完全阻断。肾上腺素或沙丁胺醇引起的右心房正性变时和变力反应被两种拮抗剂适度抑制,但ICI 118,551抑制窦性心率增加比抑制心房张力增加更有效。(摘要截短于250字)

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