Warfarin inhibition of vitamin K 2,3-epoxide reductase in rat liver microsomes

• Published in: Biochemistry (Easton) Vol. 22; no. 24; pp. 5655 - 5660
• Main Authors: Fasco, Michael J, Principe, Louise M, Walsh, William A, Friedman, Paul A
• Format: Journal Article
• Language: English
• Published: Washington, DC American Chemical Society 01-11-1983
• Subjects: Analytical, structural and metabolic biochemistry; Animals; Biological and medical sciences; Chemical Phenomena; Chemistry; Dithiothreitol - pharmacology; Enzymes and enzyme inhibitors; Fundamental and applied biological sciences. Psychology; Male; Microsomes, Liver - enzymology; Mixed Function Oxygenases - antagonists & inhibitors; Oxidoreductases; Rats; Rats, Inbred Strains; Vitamin K 1 - analogs & derivatives; Vitamin K 1 - metabolism; Vitamin K Epoxide Reductases; Warfarin - pharmacology; Vertebrata; Mammalia; Rat; Enzyme; Liver; Rodentia; Inhibition; Microsome; Metabolism; Coumarin; Vitamin K
• ISSN: 0006-2960; 1520-4995
• DOI: 10.1021/bi00293a031

Warfarin is a potent inhibitor of vitamin K 2,3-epoxide reduction to vitamin K in vitro and in vivo. Dithiothreitol, an in vitro reductant for the vitamin K 2,3-epoxide reductase, antagonizes inhibition of the reductase by warfarin via mechanisms that have not been determined [Zimmermann, A., & Matschiner, J. T. (1974) Biochem. Pharmacol. 23, 1033-1040]. Experiments with rat hepatic microsomes were undertaken to characterize the interactions that exist between vitamin K 2,3-epoxide, warfarin, and dithiothreitol. Increasing concentrations of dithiothreitol decreased inhibition of the reductase by warfarin. When dithiothreitol was present prior to exposure of the reductase to warfarin, there was less inhibition than when the same concentration of dithiothreitol was present after its exposure to warfarin. Moreover, maximum inhibition of the reductase by warfarin occurred at a much slower rate when dithiothreitol was present initially. Inhibition of the reductase by warfarin was greater when the substrate concentration was 100 microM vitamin K 2,3-epoxide than when it was 10 microM epoxide. On the basis of these data, we conclude that (i) dithiothreitol reduces either directly or indirectly a critical disulfide within the reductase that it reoxidized during reduction of the epoxide substrate, (ii) warfarin and vitamin K 2,3-epoxide are not competitive with respect to one another, and (iii) warfarin binding, which produces inhibition, occurs solely to the disulfide form of the reductase. Once it is bound, warfarin inhibits further reduction of the critical disulfide by dithiothreitol. Dithiothreitol therefore antagonizes warfarin by maintaining the reductase in the reduced state.