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中枢胆碱能药物WEB 1881-FU对离体犬心制剂心脏效应的药理学分析。

Pharmacological analysis of cardiac effects of a central cholinergic agent, WEB 1881-FU, in isolated canine heart preparations.

作者信息

Chiba S, Karasawa Y, Akahane K, Ren L M

机构信息

Department of Pharmacology, Shinshu University School of Medicine, Matsumoto, Japan.

出版信息

Jpn Heart J. 1990 Mar;31(2):217-25. doi: 10.1536/ihj.31.217.

Abstract

The cardiovascular effects of the novel compound WEB 1881-FU (4-amino-methyl-1-benzyl-pyrrolidine-2-one-fumarate) were investigated using cross-circulated dog atrial preparations. Intravenous injections of WEB 1881 induced a hypotensive effect with slight tachycardia at a large dose in anesthetized dogs. At the same time, it produced slight positive chronotropic and inotropic effects in the isolated atrium perfused with the donor's arterial blood. Direct injections of WEB 1881 into the sinus node artery of the isolated and perfused atrium induced positive chrono- and inotropic effects in a relatively small dose range. At higher doses, it caused biphasic chrono- and inotropic effects, i.e., initial brief negative effects followed by long-lasting positive chrono- and inotropic effects. The negative chrono- and inotropic responses to WEB 1881 were not blocked by atropine in doses which significantly suppressed ACh-induced negative chrono- and inotropic responses. The positive chrono- and inotropic responses to WEB 1881 were significantly inhibited either by a beta-blocker (propranolol) or by an uptake blocker (imipramine). From these results, it is concluded that WEB 1881 has a tyramine-like, catecholamine releasing property. Although a large dose of WEB 1881 has a direct cardiac depressant action, it does not affect muscarinic mechanisms in the heart.

摘要

利用交叉循环犬心房制备物研究了新型化合物WEB 1881-FU(4-氨基甲基-1-苄基吡咯烷-2-酮富马酸盐)的心血管效应。静脉注射WEB 1881可使麻醉犬在大剂量时出现降压作用并伴有轻微心动过速。同时,它对用供体动脉血灌注的离体心房产生轻微的正性变时和变力作用。将WEB 1881直接注射到离体灌注心房的窦房结动脉中,在相对较小的剂量范围内可引起正性变时和变力作用。在较高剂量时,它会引起双相变时和变力作用,即最初短暂的负性作用随后是持久的正性变时和变力作用。对WEB 1881的负性变时和变力反应不会被能显著抑制乙酰胆碱诱导的负性变时和变力反应的阿托品剂量所阻断。对WEB 1881的正性变时和变力反应可被β受体阻滞剂(普萘洛尔)或摄取阻滞剂(丙咪嗪)显著抑制。从这些结果可以得出结论,WEB 1881具有类似酪胺的儿茶酚胺释放特性。虽然大剂量的WEB 1881具有直接的心脏抑制作用,但它不影响心脏中的毒蕈碱机制。

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