首页> 外文OA文献 >The effects of beta-adrenoceptor antagonists and levomepromazine on the metabolic ratio of debrisoquine.
【2h】

The effects of beta-adrenoceptor antagonists and levomepromazine on the metabolic ratio of debrisoquine.

机译:β-肾上腺素能受体拮抗剂和左旋丙嗪对地溴异喹代谢率的影响。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The in vivo inhibitory effect of five beta-adrenoceptor antagonists and levomepromazine on debrisoquine metabolism was assessed in 37 subjects. The debrisoquine phenotyping test was performed before and after 7 days' treatment with oxprenolol (40 mg three times daily), propranolol (20 mg three times daily), timolol (10 mg twice daily), pindolol (5 mg twice daily), metoprolol (50 mg twice daily) or levomepromazine (10 mg daily), each of which was given to six-seven subjects. No clear change in the urinary metabolic ratio of debrisoquine/4-OH-debrisoquine (MR) was seen with any of the single beta-adrenoceptor antagonist treatments, but the MR value increased significantly when all beta-adrenoceptor blocker treatments were considered together. Debrisoquine metabolism was clearly impaired after levomepromazine 10 mg daily for 7 days; the mean MR increased from 1.24 +/- 1.6 to 4.70 +/- 5.23 (P = 0.018) and the excretion of 4-hydroxydebrisoquine decreased from 0.92 +/- 0.46 mg to 0.31 +/- 0.19 mg (P = 0.043). Thus, levomepromazine changes MRs towards those characteristic of phenotypically poor metabolizers, but beta-adrenoceptor antagonists at the doses examined have only a marginal effect.
机译:在37位受试者中评估了5种β-肾上腺素受体拮抗剂和左旋丙嗪对debrisoquine代谢的体内抑制作用。在用甲泼尼龙(40 mg每天3次),普萘洛尔(20 mg每天3次),噻吗洛尔(10 mg每天2次),哌多洛尔(5 mg每天2次),美托洛尔(每天两次)治疗7天之前和之后进行debrisoquine表型测试。每天两次50毫克)或左丙嗪(每天10毫克),每组分别给予67名受试者。没有观察到任何单一的β-肾上腺素受体拮抗剂治疗的情况下,debrisoquine / 4-OH-debrisoquine(MR)的尿代谢率没有明显变化,但是当同时考虑所有β-肾上腺素受体阻滞剂治疗时,MR值显着增加。每天服用10毫克左旋丙嗪7天后,地溴异喹的代谢明显受损。平均MR从1.24 +/- 1.6升高到4.70 +/- 5.23(P = 0.018),4-羟基异异喹的排泄从0.92 +/- 0.46 mg降低到0.31 +/- 0.19 mg(P = 0.043)。因此,左旋丙嗪将MRs改变为表型较弱的代谢物的特征,但是β-肾上腺素受体拮抗剂在所研究的剂量下仅具有边际作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号