Abstract
When administered in high dosages, salicylate acts as a vitamin K-antagonist: it induces a decrease of the plasma concentration of the Gla-containing coagulation factors and an accumulation of microsomal substrates for vitamin K-dependent carboxylase in the liver and in the lung. In vitro the drugs inhibit the DTT-dependent reductases which mediate the reduction of vitamin K epoxide and vitamin K quinone. NADH-dependent reductase and vitamin K-dependent carboxylase are not inhibited.
Publication types
-
Comparative Study
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Animals
-
Blood Coagulation Factors / blood
-
Carboxy-Lyases / metabolism
-
Dose-Response Relationship, Drug
-
Liver / drug effects
-
Liver / metabolism
-
Lung / drug effects
-
Lung / metabolism
-
Oxidoreductases / metabolism
-
Rats
-
Salicylates / pharmacology*
-
Vitamin K / antagonists & inhibitors*
-
Warfarin / pharmacology*
Substances
-
Blood Coagulation Factors
-
Salicylates
-
Vitamin K
-
Warfarin
-
Oxidoreductases
-
Carboxy-Lyases