心肌中丙基苄基胆碱对芥菜敏感和耐药的毒蕈碱受体。

I Takayanagi, K Koike, K Saito
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引用次数: 5

摘要

1. 用电驱动豚鼠左心房作为含有m2 -胆碱受体的实验器官。2. 丙基苄基胆碱芥(PrBCM)给心房治疗10和30 min,可逐渐抑制毒蕈碱类完全激动剂丙二醇和丁基三甲基铵的浓度-反应曲线;10(-6) M)。用PrBCM处理50分钟后,对它们的曲线没有进一步明显的抑制作用。3.用PrBCM治疗心房30分钟完全抑制部分激动剂匹罗卡品的浓度-反应曲线。在PrBCM治疗30分钟后的心房中,匹罗卡品改变了完全激动剂的浓度-反应曲线,表明存在竞争性拮抗剂。4. 这些结果表明存在两种m2受体亚型;prbcm敏感的和-抗性的,并且完全激动剂通过两种受体的相互作用抑制抽搐,而部分激动剂通过激活prbcm敏感的受体产生抑制作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Propylbenzilylcholine mustard-sensitive and -resistant muscarinic receptors in cardiac muscle.

1. A left atrium of guinea pig driven electrically was used as a test organ containing M2-cholinoceptors. 2. Concentration-response curves of carbachol and butyltrimethylammonium, muscarinic full agonists, were progressively inhibited by 10 and 30 min treatments of the atrium with propylbenzilylcholine mustard (PrBCM; 10(-6) M). The 50 min treatment with PrBCM had no further significant inhibitory effect on their curves. 3. The 30 min treatment of the atrium with PrBCM completely inhibited the concentration-response curve of pilocarpine, a partial agonist. In the atrium after the 30 min treatment with PrBCM, pilocarpine shifted the concentration-response curves of the full agonists, suggesting a competitive antagonism. 4. These results suggest an existence of two subtypes of M2-receptors; PrBCM-sensitive and -resistant ones, and that the full agonists inhibit the twitch through an interaction of both the receptors, while the partial agonist produce inhibition through an activation of PrBCM-sensitive ones.

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