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双香豆素与甲苯磺丁脲在人体中的相互作用的药代动力学分析。

Pharmacokinetic analysis of the interaction between dicoumarol and tolbutamide in man.

作者信息

Jähnchen E, Meinertz T, Gilfrich H J, Groth U

出版信息

Eur J Clin Pharmacol. 1976 Sep 30;10(5):349-56. doi: 10.1007/BF00565625.

Abstract

The effect of repeated administration of tolbutamide on the elimination and anticoagulant action of a single oral dose of dicoumarol 600 mg was studied in four healthy male subjects using a crossover design. In all subjects the plasma concentration of dicoumarol in the postabsorptive phase was lower during concomitant tolbutamide treatment. However, the subjects differed with respect to the elimination kinetics of dicoumarol and the effect of tolbutamide on some of the measured pharmacokinetic paramaters. In two subjects dicoumarol was eliminated by apparent first-order kinetics. Tolbutamide led to a pronounced increase in the elimination rate and a shift in the plasma concentration-response relationship towards a lower concentration of dicoumarol. The total hypoprothrombinaemic effect per dose of dicoumarol was not affected. The decline in the dicoumarol concentration in plasma in the other two subjects was concentration-dependent. Apparent first-order kinetics were observed only at plasma concentrations below 10 mg/L. Tolbutamide treatment did not markedly affect the slope of the terminal portion of the plasma concentration vs. time curve, but diminished the area under the total curve. The plasma concentration-response relationship of dicoumarol was not affected by tolbutamide, but there was a small decrease in the area under the anticoagulant effect vs. time curve. The plateau level of tolbutamide in plasma increased considerable in all subjects after administration of one dose of dicoumarol. Thus, simultaneous administration of tolbutamide and dicoumarol to man often causes no changes in the anticoagulant activity of dicoumarol, but this is due not to lack of interaction of the drugs but to the complexity of their interactions, involving processes that may counteract each other.

摘要

采用交叉设计,在4名健康男性受试者中研究了重复给予甲苯磺丁脲对单次口服600mg双香豆素的消除及抗凝作用的影响。在所有受试者中,同时给予甲苯磺丁脲治疗时,吸收后相双香豆素的血浆浓度较低。然而,受试者在双香豆素的消除动力学以及甲苯磺丁脲对某些测得的药代动力学参数的影响方面存在差异。在两名受试者中,双香豆素按表观一级动力学消除。甲苯磺丁脲导致消除速率显著增加,血浆浓度-反应关系向较低双香豆素浓度偏移。每剂双香豆素的总低凝血酶原血症作用未受影响。另外两名受试者血浆中双香豆素浓度的下降呈浓度依赖性。仅在血浆浓度低于10mg/L时观察到表观一级动力学。甲苯磺丁脲治疗未显著影响血浆浓度-时间曲线终末部分的斜率,但减小了总曲线下面积。双香豆素的血浆浓度-反应关系不受甲苯磺丁脲影响,但抗凝作用-时间曲线下面积略有减小。给予一剂双香豆素后,所有受试者血浆中甲苯磺丁脲的平台水平均显著升高。因此,甲苯磺丁脲和双香豆素同时给予人体时,双香豆素的抗凝活性通常无变化,但这并非由于药物缺乏相互作用,而是由于它们相互作用的复杂性,涉及可能相互抵消的过程。

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