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通过自动化设备评估普萘洛尔、吲哚洛尔和卡替洛尔对犬原位心脏房室传导的影响。

Effects on atrio-ventricular conduction of propranolol, pindolol and carteolol in the dog heart in situ as assessed by automated devices.

作者信息

Taira N, Iijima T, Narimatsu A, Satoh K, Yanagisawa T

出版信息

Jpn J Pharmacol. 1978 Jun;28(3):473-83. doi: 10.1254/jjp.28.473.

Abstract

In open-chest dogs the heart rate was controlled at 150 beats/min and drugs were given intravenously. Propranolol (30 microgram/kg--1 mg/kg) prolonged the atrioventricular (A-V) conduction time and functional refractory period of the A-V conduction system (FRP) by blockade of the existing tone of the sympathetic nerves to the heart. The prolongation of the two parameters by the non-specific depressant action of propranolol was evident only at 3 mg/kg. Propranolol (3--30 microgram/kg) shortened the A-V conduction time in the heart deprived of the vagal and sympathetic tone, suggesting some sort of sympathomimetic effect. Pindolol in a wide range of doses (0.3--300 microgram/kg) exerted virtually no effect on the A-V conduction time and FRP, and its non-specific depressant action was apparent only at 3 mg/kg. Carteolol slightly prolonged the A-V conduction time and FRP only in low doses (1--10 microgram/kg), and in high doses (30 microgram/kg--1 mg/kg) it shortened the two parameters, reflecting its predominant sympathomimetic action.

摘要

在开胸犬中,心率控制在150次/分钟,药物经静脉给药。普萘洛尔(30微克/千克 - 1毫克/千克)通过阻断心脏交感神经的现有张力,延长了房室(A-V)传导时间和房室传导系统的功能不应期(FRP)。仅在3毫克/千克时,普萘洛尔的非特异性抑制作用导致这两个参数延长才明显。普萘洛尔(3 - 30微克/千克)使去除迷走神经和交感神经张力的心脏中的A-V传导时间缩短,提示某种拟交感神经效应。吲哚洛尔在广泛的剂量范围(0.3 - 300微克/千克)对A-V传导时间和FRP几乎没有影响,其非特异性抑制作用仅在3毫克/千克时明显。卡替洛尔仅在低剂量(1 - 10微克/千克)时轻微延长A-V传导时间和FRP,而在高剂量(30微克/千克 - 1毫克/千克)时缩短这两个参数,反映了其主要的拟交感神经作用。

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