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麻醉剂氯胺酮对双壳贝类软体动物瓦氏獭蛤心脏作用方式的研究。

Investigation of the mode of action of the anaesthetic agent, ketamine, in the heart of the bivalve mollusc Tapes watlingi.

作者信息

Jamieson D D, Lander J

出版信息

Comp Biochem Physiol C Comp Pharmacol Toxicol. 1984;77(1):109-14. doi: 10.1016/0742-8413(84)90138-5.

Abstract

In the isolated heart preparation from the bivalve mollusc Tapes watlingi the anaesthetic agent ketamine produced two distinct effects; a positive inotropic effect and bradycardia. The dose-dependent positive inotropic effect was considered to be a direct effect on the cardiac muscle since it was not blocked by antagonists specific for the excitatory actions of acetylcholine, dopamine, serotonin and octopamine. Verapamil, a calcium ion antagonist, did not affect the inotropic response. The bradycardia caused by ketamine was blocked by inhibitors specific for the acetylcholine receptor but not by specific antagonists to the inhibitory dopamine receptor.

摘要

在双壳贝类软体动物瓦氏獭蛤的离体心脏标本中,麻醉剂氯胺酮产生了两种不同的效应:正性肌力作用和心动过缓。剂量依赖性的正性肌力作用被认为是对心肌的直接作用,因为它不会被针对乙酰胆碱、多巴胺、血清素和章鱼胺兴奋作用的拮抗剂所阻断。钙离子拮抗剂维拉帕米不影响肌力反应。氯胺酮引起的心动过缓可被乙酰胆碱受体特异性抑制剂阻断,但不能被多巴胺抑制性受体特异性拮抗剂阻断。

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