Suppr超能文献

普萘洛尔与地西泮、劳拉西泮和阿普唑仑的相互作用。

Propranolol interactions with diazepam, lorazepam, and alprazolam.

作者信息

Ochs H R, Greenblatt D J, Verburg-Ochs B

出版信息

Clin Pharmacol Ther. 1984 Oct;36(4):451-5. doi: 10.1038/clpt.1984.203.

Abstract

Healthy subjects received single doses of diazepam (5 to 10 mg iv), lorazepam (2 mg iv), or alprazolam (1 mg orally) on two occasions, once in the control state and once with propranolol, 80 mg three times a day. Compliance with the propranolol regimen was verified by measurement of serum propranolol levels (overall means: 100 ng/ml) and by reduction in sensitivity to intravenous metaproterenol to one-thirtieth that of the control value. Propranolol prolonged diazepam elimination t1/2 (58 and 49 hr), reduced its clearance (0.20 and 0.24 ml/min/kg), and increased the 168-hr AUC for desmethyldiazepam, the major metabolite of diazepam (5.63 and 4.81 micrograms/ml . hr). Propranolol had no significant effect on lorazepam t1/2 (13.2 and 12.7 hr) or clearance (1.33 and 1.36 ml/min/kg), nor on alprazolam t1/2 (15.9 and 18.5 hr) or clearance (1.1 and 0.8 ml/min/kg). Thus propranolol induces a small but significant reduction in clearance of diazepam, biotransformed mainly by the oxidative reaction of N-demethylation. Propranolol does not impair lorazepam clearance by glucuronide conjugation nor that of alprazolam by aliphatic hydroxylation.

摘要

健康受试者分两次接受单剂量的地西泮(静脉注射5至10毫克)、劳拉西泮(静脉注射2毫克)或阿普唑仑(口服1毫克),一次在对照状态下,一次在服用普萘洛尔(每天三次,每次80毫克)时。通过测量血清普萘洛尔水平(总体均值:100纳克/毫升)以及将静脉注射间羟异丙肾上腺素的敏感性降低至对照值的三十分之一来验证对普萘洛尔治疗方案的依从性。普萘洛尔延长了地西泮的消除半衰期(58和49小时),降低了其清除率(0.20和0.24毫升/分钟/千克),并增加了地西泮主要代谢产物去甲地西泮的168小时曲线下面积(5.63和4.81微克/毫升·小时)。普萘洛尔对劳拉西泮的半衰期(13.2和12.7小时)或清除率(1.33和1.36毫升/分钟/千克)没有显著影响,对阿普唑仑的半衰期(15.9和18.5小时)或清除率(1.1和0.8毫升/分钟/千克)也没有显著影响。因此,普萘洛尔使主要通过N-去甲基化氧化反应进行生物转化的地西泮的清除率有小幅但显著的降低。普萘洛尔不会损害通过葡萄糖醛酸结合的劳拉西泮的清除率,也不会损害通过脂肪族羟基化的阿普唑仑的清除率。

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