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西咪替丁增加利多卡因的毒性并降低其清除率。

Increased toxicity and reduced clearance of lidocaine by cimetidine.

作者信息

Feely J, Wilkinson G R, McAllister C B, Wood A J

出版信息

Ann Intern Med. 1982 May;96(5):592-4. doi: 10.7326/0003-4819-96-5-592.

Abstract

Cimetidine reduced liver blood flow and the systemic clearance of drugs, such as propranolol, that are highly extracted by the liver. In a randomized placebo-controlled study, we examined the influence of cimetidine, 300 mg four times daily for 1 d, on the disposition of lidocaine, 1 mg/kg body weight by a 10-minute intravenous infusion. Cimetidine reduced the systemic clearance of lidocaine from 766 +/- 50 mL/min to 576 +/- 47 mL/min (p less than 0.05); the apparent volume of distribution at steady-state and the degree of plasma protein binding of lidocaine also were decreased. Five of the six subjects noted lidocaine toxicity during the cimetidine infusion in contrast to one subject on the placebo day. The peak lidocaine concentration (mean +/- SE) was 50% +/- 10% higher when subjects received cimetidine. This study provides additional evidence that the effect of cimetidine on the elimination of other drugs has multiple factors, and shows a previously unrecognized mechanism, involving altered initial drug distribution, whereby the interaction of cimetidine with other drugs may cause toxicity.

摘要

西咪替丁可减少肝血流量以及肝脏对普萘洛尔等高度提取药物的全身清除率。在一项随机安慰剂对照研究中,我们考察了每日4次、每次300 mg、共服用1天的西咪替丁对通过10分钟静脉输注给予的1 mg/kg体重利多卡因处置的影响。西咪替丁使利多卡因的全身清除率从766±50 mL/分钟降至576±47 mL/分钟(p<0.05);稳态时的表观分布容积和利多卡因的血浆蛋白结合程度也降低。与安慰剂日的1名受试者相比,6名受试者中有5名在输注西咪替丁期间出现利多卡因毒性。当受试者接受西咪替丁时,利多卡因的峰值浓度(均值±标准误)高出50%±10%。本研究提供了更多证据表明西咪替丁对其他药物消除的影响具有多种因素,并显示了一种先前未被认识的机制,涉及初始药物分布改变,据此西咪替丁与其他药物的相互作用可能导致毒性。

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