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β-肾上腺素受体阻断剂对实验性糖尿病大鼠离体心房肌和乳头肌的影响。

Effects of beta-adrenoceptor blocking agents on isolated atrial and papillary muscles from experimentally diabetic rats.

作者信息

Nagamine F, Murakami K, Mimura G, 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. 1989 Jan;49(1):67-76. doi: 10.1254/jjp.49.67.

Abstract

Effects of propranolol and atenolol on isoproterenol-induced responses of isolated atrial and papillary muscles from experimentally diabetic rats were examined. Male Sprague-Dawley rats were divided into the diabetic group (DM) which received streptozotocin 60 mg/kg, i.v. and the control group (C) which received vehicle i.v. At 6 weeks after, the right atrial or right ventricular papillary muscle was isolated, and the beating rate (R) in the atrium or isometric force development (F) and its first derivatives (+/- dF/dt) in the papillary muscle under pacing were recorded. Basal R was less frequent in DM than in C, but ED50 values for isoproterenol-induced chronotropy were not different between the two groups. Basal F and basal +/- dF/dt were not different between the two groups, but isoproterenol-induced increases in F and +/- dF/dt were less in DM than in C. ED50 values in F and +dF/dt were not different between the two groups. Propranolol and atenolol shifted the concentration-response curves in R, F and +/- dF/dt for isoproterenol to the right in both groups. pA2 values of propranolol and atenolol for each parameter were not different between the two groups. Results indicate that propranolol and atenolol exert the same beta-adrenoceptor blocking potency in both diabetic and non-diabetic hearts of rats.

摘要

研究了普萘洛尔和阿替洛尔对实验性糖尿病大鼠离体心房和乳头肌异丙肾上腺素诱导反应的影响。雄性斯普拉格-道利大鼠分为糖尿病组(DM),静脉注射链脲佐菌素60mg/kg,和对照组(C),静脉注射溶媒。6周后,分离右心房或右心室乳头肌,记录心房的搏动频率(R)或乳头肌在起搏下的等长力发展(F)及其一阶导数(+/- dF/dt)。DM组的基础R频率低于C组,但两组间异丙肾上腺素诱导变时性的ED50值无差异。两组间基础F和基础+/- dF/dt无差异,但DM组异丙肾上腺素诱导的F和+/- dF/dt增加低于C组。两组间F和+dF/dt的ED50值无差异。普萘洛尔和阿替洛尔使两组中异丙肾上腺素在R、F和+/- dF/dt方面的浓度-反应曲线右移。两组间普萘洛尔和阿替洛尔各参数的pA2值无差异。结果表明,普萘洛尔和阿替洛尔在大鼠糖尿病和非糖尿病心脏中发挥相同的β-肾上腺素能受体阻断效能。

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