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大鼠中阿米替林和去甲替林与华法林的药物相互作用。

Drug interactions of amitriptyline and nortriptyline with warfarin in the rat.

作者信息

Loomis C W, Racz W J

出版信息

Res Commun Chem Pathol Pharmacol. 1980 Oct;30(1):41-58.

PMID:7433768
Abstract

Treatment of rats with amitriptyline or nortriptyline for 6 days at 6, 15 and 30 mg/kg produced no increases in the activities of aniline hydroxylase and aminopyrine N-demethylase or the content of microsomal protein and cytochrome P-450. Significant decreases in aminopyrine N-demethylase activity and cytochrome P-450 content were observed at 30 mg/kg. This inhibition of activity appeared to be at the level of cytochrome P-450 and not a cytotoxic effect in liver cells. Concomitant administration of amitriptyline or nortriptyline (6, 15 and 30 mg/kg)with warfarin to rats produced a dose dependent increase in the prothrombin time. At high doses of the tricyclic antidepressants, these increases in prothrombin time correlated with increases observed in the plasma half-life of warfarin. In vitro studies suggested that amitriptyline and nortriptyline inhibited the metabolism of warfarin. A double-reciprocal plot (Lineweaver-Burk method) showed this inhibition to be competitive. Nortriptyline produced greater inhibition of warfarin metabolism than amitriptyline and correspondingly greater enhancement of the anticoagulant effect.

摘要

以6、15和30mg/kg的剂量给大鼠服用阿米替林或去甲替林6天,未导致苯胺羟化酶和氨基比林N-脱甲基酶的活性、微粒体蛋白含量及细胞色素P-450增加。在30mg/kg剂量时,观察到氨基比林N-脱甲基酶活性和细胞色素P-450含量显著降低。这种活性抑制似乎发生在细胞色素P-450水平,而非肝细胞的细胞毒性作用。给大鼠同时服用阿米替林或去甲替林(6、15和30mg/kg)与华法林,会使凝血酶原时间呈剂量依赖性增加。在三环类抗抑郁药的高剂量下,这些凝血酶原时间的增加与华法林血浆半衰期的增加相关。体外研究表明,阿米替林和去甲替林抑制华法林的代谢。双倒数作图(Lineweaver-Burk法)显示这种抑制为竞争性抑制。去甲替林对华法林代谢的抑制作用比阿米替林更强,相应地对抗凝作用的增强也更大。

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