Suppr超能文献

章鱼胺正性变时性和变力性反应的药理学分析。

Pharmacologic analysis of positive chronotropic and inotropic responses to octopamine.

作者信息

Chiba S

出版信息

Tohoku J Exp Med. 1976 Mar;118(3):247-53. doi: 10.1620/tjem.118.247.

Abstract

Effects of octopamine on sinus rate and atrial contractility were investigated using the isolated atrium preparation of the dog which perfused with heparinized arterial blood led from a support dog. When octopamine, dopamine or norepinephrine was administered into the cannulated sinus node artery, positive chronotropic and inotropic responses were dose-relatedly induced from 0.1 mug, 0.1 mug or 0.01 mug, respectively. The D.R.50 values (dose ratio at 50% maximum response) of octopamine, dopamine and norepinephrine are roughly 30-100: 30:1, respectively. The duration of action of octopamine was longest. Effects induced by octopamine were blocked by an adrenergic beta-blocking agent, alprenolol. Desmethyl-imipramine treatment significantly suppressed octopamine-induced effects but rather enhanced norepinephrine-induced ones. Octopamine-induced effects were not influenced by tetrodotoxin which blocked those induced by nicotine. From these results, it is concluded that positive chronotropic and inotropic responses to octopamine are mainly due to a tyramine-like action.

摘要

使用从供血犬引出的肝素化动脉血灌注的犬离体心房标本,研究了章鱼胺对窦性心率和心房收缩力的影响。当将章鱼胺、多巴胺或去甲肾上腺素注入插管的窦房结动脉时,分别从0.1微克、0.1微克或0.01微克开始,剂量依赖性地诱导出正性变时和变力反应。章鱼胺、多巴胺和去甲肾上腺素的D.R.50值(最大反应50%时的剂量比)分别约为30 - 100:30:1。章鱼胺的作用持续时间最长。章鱼胺诱导的效应被肾上腺素能β受体阻滞剂阿普洛尔阻断。去甲丙咪嗪处理显著抑制了章鱼胺诱导的效应,但却增强了去甲肾上腺素诱导的效应。章鱼胺诱导的效应不受河豚毒素的影响,而河豚毒素可阻断尼古丁诱导的效应。从这些结果可以得出结论,对章鱼胺的正性变时和变力反应主要是由于类似酪胺的作用。

相似文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验