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苯基丁氮酮与华法林在犬体内的相互作用。

Phenylbutazone-warfarin interaction in the dog.

作者信息

Bachmann K A, Burkman A M

出版信息

J Pharm Pharmacol. 1975 Nov;27(11):832-6. doi: 10.1111/j.2042-7158.1975.tb10225.x.

Abstract

The administration of phenylbutazone together with warfarin to dogs resulted in an elevation of the free fraction of warfarin in the plasma from 2-6 to 8-0% thus providing direct support for the notion that phenylbutazone induced inhibition of warfarin binding to plasma proteins. This inhibition as evaluated by a kinetic method was accompanied by a two-fold decrease in the plasma half-life of warfarin from 18-4 h in control animals to 9-6 h in phenylbutazone-treated animals. Marked increases in warfarin-induced hypoprothrombinaemia were observed when at doses up to 8 mg kg-1 (orally) it was given with phenylbutazone (50 mg kg-1, orally). The unbound fraction of warfarin in canine plasma ranged from 1-7 to 4-3% indicating individual differences in the extent of the plasma binding of warfarin in the dog.

摘要

给狗同时施用保泰松和华法林,导致血浆中华法林的游离分数从2% - 6%升高到8% - 0%,从而直接支持了保泰松诱导抑制华法林与血浆蛋白结合这一观点。通过动力学方法评估,这种抑制伴随着华法林血浆半衰期从对照动物的18.4小时降至保泰松处理动物的9.6小时,降低了两倍。当华法林以高达8毫克/千克(口服)的剂量与保泰松(50毫克/千克,口服)一起给药时,观察到华法林诱导的低凝血酶原血症显著增加。犬血浆中华法林的未结合分数在1.7%至4.3%之间,表明狗对华法林血浆结合程度存在个体差异。

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