首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >The classification of beta-adrenoceptors in isolated ring preparations of canine coronary arteries.
【2h】

The classification of beta-adrenoceptors in isolated ring preparations of canine coronary arteries.

机译:β-肾上腺素受体在犬冠状动脉离体环制剂中的分类。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Relaxant responses to the beta-adrenoceptor agonists isoprenaline, fenoterol, noradrenaline or procaterol were obtained on isolated ring preparations of canine coronary arteries contracted with KCl (20 mM) or 5-hydroxytryptamine (3 microM). On left circumflex arterial preparations, Schild plots for the selective antagonists atenolol (beta 1-selective) or ICI 118,551 (beta 2-selective), when using noradrenaline or fenoterol as agonist, were superimposed. This suggested that only one subtype of beta-adrenoceptor was involved in the responses. The pA2 values on left circumflex artery preparations were: atenolol, noradrenaline as agonist 6.98, fenoterol as agonist 6.71; ICI 118, 551, noradrenaline as agonist 6.66, fenoterol as agonist 7.04. These data indicated that the beta-adrenoceptor subtype was beta 1. The relative potencies of isoprenaline: noradrenaline: fenoterol were left circumflex 100: 10.0: 2.3, left ventricular branch 100: 9.7: 2.0, septal branch 100: 10.9: 2.5. These data confirmed that beta 1-adrenoceptors were involved in the responses of all three arterial preparations. On preparations of left circumflex artery, left ventricular branch and septal branch, responses were obtained to high concentrations (1 to 100 microM) but not to low concentrations (0.001 to 0.1 microM) of procaterol. This observation confirmed the absence of beta 2-adrenoceptors in these arteries. Responses of left circumflex artery to isoprenaline were potentiated by the extraneuronal uptake inhibitor drugs, corticosterone and metanephrine.(ABSTRACT TRUNCATED AT 250 WORDS)
机译:在与KCl(20 mM)或5-hydroxytryptamine(3 microM)收缩的犬冠状动脉的分离环制剂上获得了对β-肾上腺素受体激动剂异戊二烯,非诺特罗,去甲肾上腺素或丙卡特罗的松弛反应。在左旋气支动脉制剂上,当使用去甲肾上腺素或非诺特罗作为激动剂时,选择性阻滞剂阿替洛尔(β1选择性)或ICI 118,551(β2选择性)的Schild图叠加。这表明应答中仅涉及一种β-肾上腺素受体亚型。左旋支动脉制剂的pA2值为:阿替洛尔,去甲肾上腺素作为激动剂6.98,非诺特罗作为激动剂6.71; ICI 118、551,去甲肾上腺素作为激动剂6.66,非诺特罗作为激动剂7.04。这些数据表明,β-肾上腺素受体亚型为β1。异丙肾上腺素:去甲肾上腺素:非诺特罗的相对效力为左旋支100:10.0:2.3,左心室支100:9.7:2.0,间隔支100:10.9:2.5。这些数据证实,β1肾上腺素能受体参与了所有三种动脉制剂的反应。在准备左旋支动脉,左心室分支和隔中分支时,获得了对高浓度(1至100 microM)但对低浓度(0.001至0.1 microM)丙卡特罗的响应。该观察结果证实这些动脉中不存在β2肾上腺素能受体。神经外摄取抑制剂药物,皮质酮和间肾上腺素能增强左旋支动脉对异丙肾上腺素的反应(摘要截断为250个单词)

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号