Induction of cyclooxygenase-a (COX-2) in ischemic myocardium is thought to
increase the production of proinflammatory prostanoids and contribute signi
ficantly to the ischemic inflammation. Left ventricular myocardial infarcti
on (MI) was created by ligating the left coronary artery in Lewis rats. Hem
odynamic measurements at 4 weeks showed better cardiac function in the grou
p treated with a selective COX-2 inhibitor (DFU; 5 mg/kg/day) for 2 weeks a
fter induction of MI compared to the vehicle treated group. These results s
uggest that induction of COX-2 contributes to myocardial dysfunction, and t
hat selective inhibition of COX-2 could constitute an important therapeutic
target for the treatment of MI. (C) 2000 Academic Press.