摘要
10例正常受试者口服普蔡洛尔10mg,tid,持续7d后,异丙基肾上腺素的变时性剂量(chronotropicdose_(25),CD_(25)从1.4±0.5μg增加到8.8±4.9μg,平均β-受体阻滞指数为7.1;卧位择时心率明显减慢,安替比林代谢受到抑制。说明短期小量使用普蔡洛尔,能产生β-受体阻滞作用和抑制安替比林代谢。
After taking propranolol 10mg,thrice daily,for 7 days,the chronotropic dose_(25)(CD_(25))of isoproterenol was increased from 1.4±0.5μg to 8.8±4.9μg in 10 volunteers;the meanβ-receptor blocking index was 7.1.The chrono-heart rate in supine position was obviously de-creased and antipyrine metabolism inhibited.The results indicated that the use of propranolol inshort-term and small dose could produce the β-receptor blocking effect and the inhibition of antipyrine metabolism.
出处
《中国药学杂志》
CAS
CSCD
北大核心
1994年第6期337-340,共4页
Chinese Pharmaceutical Journal
关键词
普萘洛尔
安替比林
心脏反应
propranolol,isoproterenol,cardiac chronotropic response,antipyrine