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Effects of Selective Cyclooxygenase-2 Inhibition on Vascular Responses and Thrombosis in Canine Coronary Arteries
Author(s) -
James K. Hennan,
Huang Jin,
Terrance D. Barrett,
Edward M. Driscoll,
David Willens,
Andrew M. Park,
Leslie J. Crofford,
Benedict R. Lucchesi
Publication year - 2001
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/hc3301.092790
Subject(s) - medicine , prostacyclin , celecoxib , cyclooxygenase , arachidonic acid , vasodilation , aspirin , thrombosis , endothelium , pharmacology , endocrinology , biochemistry , enzyme , chemistry
Prostanoid synthesis via the action of cyclooxygenase-2 (COX-2) is a component of the inflammatory response. Prostacyclin, a product of COX-2 in vascular endothelium, has important physiological roles, such as increasing blood flow to injured tissues, reducing leukocyte adherence, and inhibiting platelet aggregation. We examined the possibility that selective COX-2 inhibition could suppress the protective effects of prostacyclin, resulting in an alteration of the hemostatic balance and vascular tone.

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