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维生素K1 2,3-环氧化物还原酶的抑制与华法林导致的凝血因子活性降低之间的关系。

The relationship between inhibition of vitamin K1 2,3-epoxide reductase and reduction of clotting factor activity with warfarin.

作者信息

Choonara I A, Malia R G, Haynes B P, Hay C R, Cholerton S, Breckenridge A M, Preston F E, Park B K

机构信息

Department of Pharmacology and Therapeutics, University of Liverpool.

出版信息

Br J Clin Pharmacol. 1988 Jan;25(1):1-7. doi: 10.1111/j.1365-2125.1988.tb03274.x.

Abstract

1 The effect of low dose steady state warfarin (0.2 mg and 1 mg daily) on clotting factor activity and vitamin K1 metabolism was studied in seven healthy volunteers. 2 Steady state plasma warfarin concentrations were 41-99 ng ml-1 for the 0.2 mg dose and 157-292 ng ml-1 for the 1 mg dose. 3 There was a significant prolongation of the mean prothrombin time (0.9 s) after 1 mg warfarin daily, but no significant change in prothrombin time after 0.2 mg warfarin daily. There was no significant change in individual clotting factor activity (II, VII, IX or X) with either dose of warfarin. 4 Following the administration of a pharmacological dose of vitamin K1 (10 mg), all seven volunteers had detectable levels of vitamin K1 2,3-epoxide with both doses of warfarin (Cpmax 31-409 ng ml-1). 5 Both the Cpmax and the AUC for vitamin K1 2,3-epoxide were significantly greater on 1 mg of warfarin daily than 0.2 mg daily (P less than 0.01). 6 The apparent dissociation between inhibition of vitamin K1 2,3-epoxide reductase and reduction of clotting factor activity, produced by warfarin, may reflect the insensitivity of functional clotting factor assays to a small reduction in clotting factor concentration.

摘要
  1. 在7名健康志愿者中研究了低剂量稳态华法林(每日0.2毫克和1毫克)对凝血因子活性和维生素K1代谢的影响。2. 0.2毫克剂量的稳态血浆华法林浓度为41 - 99纳克/毫升,1毫克剂量的为157 - 292纳克/毫升。3. 每日服用1毫克华法林后,平均凝血酶原时间显著延长(0.9秒),但每日服用0.2毫克华法林后凝血酶原时间无显著变化。两种剂量的华法林对单个凝血因子活性(II、VII、IX或X)均无显著影响。4. 给予药理剂量的维生素K1(10毫克)后,所有7名志愿者在两种剂量的华法林作用下均检测到维生素K1 2,3 - 环氧化物水平(Cpmax为31 - 409纳克/毫升)。5. 每日服用1毫克华法林时维生素K1 2,3 - 环氧化物的Cpmax和AUC均显著高于每日服用0.2毫克时(P小于0.01)。6. 华法林产生的维生素K1 2,3 - 环氧化物还原酶抑制与凝血因子活性降低之间的明显分离,可能反映了功能性凝血因子检测对凝血因子浓度小幅降低的不敏感性。

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