Literature DB >> 6149281

Indirect inhibition of vitamin K epoxide reduction by salicylate.

E Hildebrandt, J W Suttie.   

Abstract

Salicylate antagonizes the vitamin K-dependent biosynthesis of clotting factors in the rat and produces an elevation of the ratio of vitamin K epoxide to vitamin K in the liver. Vitamin K epoxide is reduced to vitamin K by a vitamin K epoxide reductase, and 1 mM salicylate was required to cause a 50% inhibition of the dithiothreitol-dependent in-vitro reduction of vitamin K epoxide by this enzyme. This enzyme was, however, inhibited 50% by as little as 70-80 microM salicylate when reducing equivalents for the reaction were furnished by endogenous cytosolic reductants. This effect on the cytosolic reductant supply was shown to be unrelated to a previously demonstrated inhibition of DT-diaphorase by salicylate. The concentrations of salicylate at which significant inhibitory effects are exerted in-vitro (50-100 microM) are below the 200 microM levels observed in the livers of rats given an anticoagulating dose of salicylate.

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Year:  1984        PMID: 6149281     DOI: 10.1111/j.2042-7158.1984.tb04903.x

Source DB:  PubMed          Journal:  J Pharm Pharmacol        ISSN: 0022-3573            Impact factor:   3.765


  1 in total

1.  Microsomal lipoamide reductase provides vitamin K epoxide reductase with reducing equivalents.

Authors:  H H Thijssen; Y P Janssen; L T Vervoort
Journal:  Biochem J       Date:  1994-01-15       Impact factor: 3.857

  1 in total

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