Suppr超能文献

布那唑嗪和酮色林对去甲肾上腺素诱导的离体灌注犬和猿猴骨骼肌动脉血管收缩的不同拮抗作用。

Different antagonistic effects of bunazosin and ketanserin on the norepinephrine-induced vasoconstriction in isolated, perfused canine and simian skeletal muscle arteries.

作者信息

Sinanović O, Chiba S

机构信息

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

出版信息

Jpn J Pharmacol. 1988 Feb;46(2):200-3. doi: 10.1254/jjp.46.200.

Abstract

Blocking activities of bunazosin and ketanserin on norepinephrine (NE)-induced vasoconstrictions were investigated in isolated, perfused canine and simian skeletal muscle arteries. NE caused an increase in perfusion pressure in a dose-related manner to almost the same extent in both canine and simian arterial preparations. Bunazosin and ketanserin inhibited NE-induced vasoconstrictions much more readily in simian arteries than in canine arteries. The mechanisms for the different adrenolytic activities of alpha 1-antagonists between these two arteries were discussed.

摘要

在离体灌注的犬和猴骨骼肌动脉中研究了布那唑嗪和酮色林对去甲肾上腺素(NE)诱导的血管收缩的阻断作用。NE在犬和猴动脉制剂中均以剂量相关的方式引起灌注压升高,升高程度几乎相同。与犬动脉相比,布那唑嗪和酮色林在猴动脉中更易抑制NE诱导的血管收缩。讨论了这两种动脉之间α1拮抗剂不同的抗肾上腺素能活性机制。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验