Suppr超能文献

普罗帕酮对兴奋传导的延缓作用。口服给药后的持续时间及剂量效应关系(作者译)

[Retardation of the excitation conduction by propaphenone. Duration and dosage effect relation after oral administration (author's transl)].

作者信息

Beck O A, Abdulla S, Hochrein H

出版信息

MMW Munch Med Wochenschr. 1975 Aug 29;117(35):1369-72.

PMID:809677
Abstract

After oral administration, and depending on dosage, propaphenone produces a uniform delay of the excitation conduction in the region of the atrium, ventricle and atrioventricular conduction. At a dosage of 5 or 10 mg/kg body-weight (1 or 2x 300 mg capsules) propaphenone causes an average delay of excitation conduction of + 11% or + 19% of the initial value, and of + 39% (capsule) or + 30% (sugar coated tablet) at 14 mg/kg body-weight. The maximum effect is attained 2.5 to 4 hours after administration. A prolongation of conduction times and consequently of the anti-arrhythmic efficacy, is still found eight hours after oral ingestion.

摘要

口服后,根据剂量不同,普罗帕酮会使心房、心室及房室传导区域的兴奋传导均匀延迟。当体重剂量为5或10mg/kg(1或2粒300mg胶囊)时,普罗帕酮会使兴奋传导平均延迟至初始值的+11%或+19%,而当体重剂量为14mg/kg时,延迟至+39%(胶囊)或+30%(糖衣片)。给药后2.5至4小时达到最大效果。口服八小时后仍可发现传导时间延长,从而抗心律失常疗效也得以延长。

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