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β2肾上腺素能受体介导的对犬房室结的正性变传导作用。

Beta 2-adrenoceptor-mediated positive dromotropic effects on atrioventricular node of dogs.

作者信息

Motomura S, Hashimoto K

机构信息

Department of Pharmacology, Yamanashi Medical College, Japan.

出版信息

Am J Physiol. 1992 Jan;262(1 Pt 2):H123-9. doi: 10.1152/ajpheart.1992.262.1.H123.

Abstract

The functional significance of beta 2-adrenoceptors in atrioventricular (AV) nodal conduction was investigated by using canine isolated blood-perfused AV node preparations. Dose-dependent shortening of the atrio-His bundle (A-H) interval by dl-procaterol hydrochloride hemihydrate (0.03-1 nmol) injected intra-arterially into the AV node artery was affected little by an infusion of dl-atenolol (10 nmol/min) into the same artery, whereas the dose-response curve for the positive dromotropic effect of procaterol was shifted markedly to the right by approximately 1.5 and 2.5 log units with ICI 118551 [erythro-dl-1-(7-methylindan-4-yloxy)-3-isopropylamino-bu tan-2-ol]- hydrochloride (1 and 10 nmol/min). The positive dromotropic effect of dl-T-1583 [alpha-(3,4,5-trimethoxyphenethylaminomethyl)-3,4-dihydroxybenzyl- alcohol] hydrochloride (30-300 pmol), a selective beta 1-adrenoceptor agonist, was shifted to the right by approximately 1.2 log units with dl-atenolol (10 nmol/min) but was affected little by ICI 118551 (10 nmol/min). The dose-response curve for l-isoproterenol hydrochloride (3-100 pmol) was shifted to the right by 0.7 log unit with ICI 118551 (10 nmol/min) and by 1.7 log units with atenolol (10 nmol/min). The dose-response curve for dl-norepinephrine (0.03-1 nmol) was shifted to the right by 1.0 log unit with atenolol only, whereas the curve for l-epinephrine (0.03-1 nmol) was shifted by 0.45 log unit with ICI 118551 (10 nmol/min). These results suggest that both beta 1- and beta 2-adrenoceptors, which coexist on the AV node, play a functional role in AV nodal conduction.

摘要

通过使用犬离体血液灌注房室结标本,研究了β2 -肾上腺素能受体在房室(AV)结传导中的功能意义。向房室结动脉内动脉注射盐酸消旋普萘洛尔半水合物(0.03 - 1 nmol)可使心房 - 希氏束(A - H)间期呈剂量依赖性缩短,而向同一动脉内输注盐酸阿替洛尔(10 nmol/min)对此影响很小;然而,对于普萘洛尔的正性变传导作用,其剂量反应曲线在注射盐酸ICI 118551 [赤式 - 消旋 - 1 -(7 - 甲基茚满 - 4 - 基氧基)- 3 - 异丙基氨基 - 丁 - 2 - 醇](1和10 nmol/min)时明显右移约1.5和2.5个对数单位。盐酸dl - T - 1583 [α -(3,4,5 - 三甲氧基苯乙胺甲基)- 3,4 - 二羟基苄醇](30 - 300 pmol)是一种选择性β1 -肾上腺素能受体激动剂,其正性变传导作用在注射盐酸阿替洛尔(10 nmol/min)时右移约1.2个对数单位,但在注射ICI 118551(10 nmol/min)时影响很小。盐酸l -异丙肾上腺素(3 - 100 pmol)的剂量反应曲线在注射ICI 118551(10 nmol/min)时右移0.7个对数单位,在注射阿替洛尔(10 nmol/min)时右移1.7个对数单位。盐酸消旋去甲肾上腺素(0.03 - 1 nmol)的剂量反应曲线仅在注射阿替洛尔时右移1.0个对数单位,而盐酸l -肾上腺素(0.03 - 1 nmol)的曲线在注射ICI 118551(10 nmol/min)时右移0.45个对数单位。这些结果表明,共存于房室结上的β1 -和β2 -肾上腺素能受体在房室结传导中均发挥功能作用。

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