Strain differences in toxicity of vitamin K antagonist warfarin in rats
Author(s) -
Jelena Djokić,
Mariinkov,
Aleksandra Popov Aleksandrov,
Ivana Mirkov,
Vesna Subota,
Luka Mihajlović,
Marija Stojadinović,
Dragana Stanić-Vučinić,
Dragan Kataranovski,
Milena Kataranovski
Publication year - 2013
Publication title -
journal of the serbian chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.227
H-Index - 45
eISSN - 1820-7421
pISSN - 0352-5139
DOI - 10.2298/jsc121114010d
Subject(s) - warfarin , vitamin k antagonist , coumarin , pharmacology , vitamin , hemostasis , strain (injury) , toxicity , antagonist , coagulation , peripheral blood mononuclear cell , medicine , chemistry , biochemistry , in vitro , receptor , atrial fibrillation , organic chemistry
Warfarin (4-hydroxy coumarin) is Vitamin K (VK) antagonist that inhibits Vitamin K-dependent (VKD) processes, such as blood coagulation. It exerts influence on some non-VKD-related activities as well. In this study, the effect of subacute (30-day) oral warfarin (2 mg L-1 and 1 mg L-1) intake on hematological parameters was examined in two rat strains, Albino Oxford (AO) and Dark Agouti (DA), that differ in their sensitivity to certain chemicals. Greater susceptibility to anticoagulant effect of 2 mg L-1 of warfarin was observed in AO rats and was associated with an increase in relevant hematological parameters in this strain. Although both strains responded to 2 mg L-1 of warfarin with quantitative changes in peripheral blood leukocytes differential bone marrow and lung responses were observed. Strain-related differences in proinflammatory activity of peripheral blood granulocytes and in mononuclear cell IFN-γ production were observed. Recognition of differences in quantitative and qualitative effects of oral warfarin on processes other than hemostasis might be of relevance for those humans who are on warfarin therapy. [Projekat Ministarstva nauke Republike Srbije, br. 173039
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