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地尔硫䓬对普萘洛尔、美托洛尔和阿替洛尔药代动力学的影响。

Effect of diltiazem on the pharmacokinetics of propranolol, metoprolol and atenolol.

作者信息

Tateishi T, Nakashima H, Shitou T, Kumagai Y, Ohashi K, Hosoda S, Ebihara A

机构信息

Department of Clinical Pharmacology, Jichi Medical School, Japan.

出版信息

Eur J Clin Pharmacol. 1989;36(1):67-70. doi: 10.1007/BF00561026.

Abstract

The pharmacokinetic interaction between diltiazem and three beta-adrenoceptor blockers propranolol, metoprolol and atenolol was investigated in healthy volunteers given diltiazem 30 mg or placebo t.d.s. for 3 days, followed by a single dose of propranolol 20 mg, metoprolol 40 mg or atenolol 50 mg. The AUCs of propranolol and metoprolol were significantly increased after diltiazem and it significantly prolonged the elimination half-life of metoprolol. In contrast, it did not significantly affect the pharmacokinetics of atenolol. Propranolol significantly decreased the resting pulse rate after diltiazem pretreatment as compared to placebo. The results indicate that diltiazem impaired the clearance of propranolol and metoprolol, which are principally metabolized by an oxidative pathway, and that the kinetic interaction between diltiazem and propranolol may partly be related to the significant reduction in the pulse rate produced by the latter.

摘要

在健康志愿者中研究了地尔硫䓬与三种β-肾上腺素受体阻滞剂普萘洛尔、美托洛尔和阿替洛尔之间的药代动力学相互作用。给健康志愿者每日三次服用30mg地尔硫䓬或安慰剂,持续3天,随后单次服用20mg普萘洛尔、40mg美托洛尔或50mg阿替洛尔。地尔硫䓬给药后,普萘洛尔和美托洛尔的AUC显著增加,且地尔硫䓬显著延长了美托洛尔的消除半衰期。相比之下,地尔硫䓬对阿替洛尔的药代动力学没有显著影响。与安慰剂相比,普萘洛尔预处理后地尔硫䓬显著降低了静息脉搏率。结果表明,地尔硫䓬损害了主要通过氧化途径代谢的普萘洛尔和美托洛尔的清除率,且地尔硫䓬与普萘洛尔之间的动力学相互作用可能部分与后者导致的脉搏率显著降低有关。

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