Circulation, Vol 81, 369-380, Copyright © 1990 by American Heart Association
NE Farber and GJ Gross
We have previously reported that inhibition of thromboxane synthesis
results in an improvement in postischemic function in stunned myocardium of
dogs. The purpose of the present study was to investigate further the
mechanism by which thromboxane synthesis inhibition improves recovery of
function in stunned myocardium (15 minutes of coronary occlusion and 3
hours of reperfusion) in barbital anesthetized dogs. The recovery of
regional myocardial wall function (percent segment shortening, % SS)
following treatment with two doses (0.5 and 10 mg/kg) of a thromboxane
receptor blocker, BM 13.505, given prior to coronary occlusion, was not
different from that of a control group (3- hour % SS of pretreatment
control, PTC, 12 +/- 11) throughout reperfusion (3-hour % SS of PTC with BM
13.505: 0.5 mg/kg 14 +/- 10; 10 mg/kg, 27 +/- 9). In contrast, the specific
thromboxane synthetase inhibitor, dazmegrel (3.0 mg/kg), significantly
improved % SS throughout reperfusion (3-hour % SS of PTC, 66 +/- 8). In
addition, while dazmegrel produced a marked decrease in thromboxane,
6-keto-PGF1 alpha was significantly increased in coronary venous blood
throughout the occlusion and reperfusion period. The cyclooxygenase
inhibitor, indomethacin, had no beneficial effect on functional recovery
(3-hour % SS of PTC, 5 +/- 6), attenuated the dazmegrel induced shunting to
prostacyclin, and completely prevented the beneficial effects of dazmegrel
on functional recovery (3-hour % SS of PTC, 17 +/- 12). Thus, a redirection
to endogenous cardioprotective prostanoids, such as prostacyclin, appears
to be responsible for the beneficial effect of thromboxane synthesis
inhibition on postischemic recovery in stunned myocardium whereas
thromboxane does not appear to be an important mediator of the stunning
phenomenon.
ARTICLES
Prostaglandin redirection by thromboxane synthetase inhibition. Attenuation of myocardial stunning in canine heart
Department of Pharmacology and Toxicology, Medical College of Wisconsin, Milwaukee 53226.
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