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丙氧芬和去甲丙氧芬对清醒家兔的心肺毒性

Cardio-respiratory toxicity of propoxyphene and norpropoxyphene in conscious rabbits.

作者信息

Lund-Jacobsen H

出版信息

Acta Pharmacol Toxicol (Copenh). 1978 Mar;42(3):171-8. doi: 10.1111/j.1600-0773.1978.tb02187.x.

Abstract

The toxic effects of alpha-d-propoxyphene (P) and its primary metabolite alpha-d-norpropoxyphene (NP) were compared to intravenous infusions (100 min.) of equimolar doses of P and NP (80 micronmol/kg equivalent to 30 mg/kg P HCl) in conscious rabbits. During P infusion severe respiratory depression and convulsions were seen in all animals, and six of the nine animals died. During NP infusion, however, only minimal respiratory depression was seen and all the animals survived. Considerable prolongation of the QRS complex and cardiac arrhythmias like intermittent A-V block and ventricular extrasystoles were seen in the ECG during both P and NP infusion, while the arterial blood pressure was unchanged. In P injection experiments (6 mg/kg P HCl), ECG changes preceded reduction in respiratory rate and during NP infusion only minor changes were seen in arterial blood gases, demonstrating that the ECG changes produced by P and NP are independent of respiratory depression. The ECG changes were found to be similar to those reported in quinidine intoxication. The QRS prolongation was markedly correlated with plasma concentrations during and after P and NP infusion. The results of the present investigation favour the hypothesis that the contribution of NP to the toxicity of oral P overdosage in man is ascribed to its cardiotoxic action whereas P is responsible for the CNS toxicity (respiratory depression and convulsions) as well as cardiotoxicity.

摘要

将等摩尔剂量的α-d-丙氧芬(P)及其主要代谢产物α-d-去甲丙氧芬(NP)(80微摩尔/千克,相当于30毫克/千克P盐酸盐)静脉输注(100分钟)给清醒的兔子,比较了P和NP的毒性作用。在输注P期间,所有动物均出现严重的呼吸抑制和惊厥,9只动物中有6只死亡。然而,在输注NP期间,仅观察到轻微的呼吸抑制,所有动物均存活。在输注P和NP期间,心电图(ECG)均出现QRS波群明显延长以及心律失常,如间歇性房室传导阻滞和室性期前收缩,而动脉血压未发生变化。在P注射实验(6毫克/千克P盐酸盐)中,ECG变化先于呼吸频率降低,且在输注NP期间,动脉血气仅出现轻微变化,表明P和NP引起的ECG变化与呼吸抑制无关。发现ECG变化与奎尼丁中毒时报告的变化相似。QRS波群延长与输注P和NP期间及之后的血浆浓度显著相关。本研究结果支持以下假说:NP对人类口服P过量中毒毒性的作用归因于其心脏毒性作用,而P则导致中枢神经系统毒性(呼吸抑制和惊厥)以及心脏毒性。

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