Literature DB >> 480184

Effects of clofibrate and warfarin alone and in combination on the disposition of vitamin K1.

T D Bjornsson, P J Meffin, S E Swezey, T F Blaschke.   

Abstract

Clofibrate may interact with warfarin by potentiating its effects on vitamin K disposition. To examine this possibility, specifically labeled [3H]vitamin K was given intravenously to four healthy volunteers under conditions of no drug administration, administration of warfarin or clofibrate alone, or co-administration of both drugs. Clofibrate alone did not affect the disposition of tritiated vitamin K. Warfarin alone produced an accumulation in plasma of substantial amounts of vitamin K epoxide, a metabolite of vitamin K which is reconverted to vitamin K by a specific reductase. Although reconversion is apparently blocked to a large extent by warfarin, the plasma disappearance of tritiated vitamin K in the presence of warfarin is almost superimpossible to that observed in the absence of drugs. Clofibrate coadministration did not result in greater accumulation of vitamin K epoxide in plasma. These results indicate that clofibrate does not enhance the inhibition of the reductase enzyme. Analysis of the tritiated vitamin K plasma disappearance data indicates that the pool size of vitamin K in the body is small, and is turned over almost 10 times daily. The vitamin K epoxide data suggest that, in the absence of drugs, a relatively small proportion of the epoxide is reconverted to the vitamin.

Entities:  

Mesh:

Substances:

Year:  1979        PMID: 480184

Source DB:  PubMed          Journal:  J Pharmacol Exp Ther        ISSN: 0022-3565            Impact factor:   4.030


  10 in total

Review 1.  Plasma protein binding displacement interactions--why are they still regarded as clinically important?

Authors:  P E Rolan
Journal:  Br J Clin Pharmacol       Date:  1994-02       Impact factor: 4.335

2.  Plasma disposition of vitamin K1 in relation to anticoagulant poisoning.

Authors:  B K Park; A K Scott; A C Wilson; B P Haynes; A M Breckenridge
Journal:  Br J Clin Pharmacol       Date:  1984-11       Impact factor: 4.335

Review 3.  Post-translational carboxylation of preprothrombin.

Authors:  B C Johnson
Journal:  Mol Cell Biochem       Date:  1981-08-11       Impact factor: 3.396

Review 4.  Clinical pharmacokinetics and pharmacodynamics of warfarin. Understanding the dose-effect relationship.

Authors:  N H Holford
Journal:  Clin Pharmacokinet       Date:  1986 Nov-Dec       Impact factor: 6.447

5.  Cyclic interconversion of vitamin K1 and vitamin K1 2,3-epoxide in man.

Authors:  H Bechtold; D Trenk; T Meinertz; M Rowland; E Jähnchen
Journal:  Br J Clin Pharmacol       Date:  1983-12       Impact factor: 4.335

6.  Enzyme induction by phenobarbitone and vitamin K1 disposition in man.

Authors:  B K Park; A C Wilson; G Kaatz; E E Ohnhaus
Journal:  Br J Clin Pharmacol       Date:  1984-07       Impact factor: 4.335

7.  Vitamin K1 metabolism in relation to pharmacodynamic response in anticoagulated patients.

Authors:  I A Choonara; A K Scott; B P Haynes; S Cholerton; A M Breckenridge; B K Park
Journal:  Br J Clin Pharmacol       Date:  1985-12       Impact factor: 4.335

Review 8.  Clinically important drug interactions with anticoagulants. An update.

Authors:  S Harder; P Thürmann
Journal:  Clin Pharmacokinet       Date:  1996-06       Impact factor: 6.447

9.  Plasma Response to Deuterium-Labeled Vitamin K Intake Varies by TG Response, but Not Age or Vitamin K Status, in Older and Younger Adults.

Authors:  Jessie L Ellis; Xueyan Fu; Ala Al Rajabi; Michael A Grusak; Martin J Shearer; Elena N Naumova; Edward Saltzman; Kathryn Barger; Sarah L Booth
Journal:  J Nutr       Date:  2019-01-01       Impact factor: 4.798

10.  Possible coumarin-like mechanism of action for cephalosporins.

Authors:  H Bechtold; J Lorenz; L S Weilemann; T Meinertz; D Trenk; K Andrassy; E Jähnchen
Journal:  Klin Wochenschr       Date:  1984-09-17
  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.