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Journal of Biomedical Engineering ; (6): 1411-1414, 2008.
Article in Chinese | WPRIM | ID: wpr-318140

ABSTRACT

The aim of the present studies was to investigate the cardioprotection of late IP at 72 h and determine the involvement of iNOS, nNOS and COX-2 in this protection. Conscious rabbits were preconditioned with three cycles of 5-minute coronary occlusion/5-minute reperfusion. The myocardial infarct area in the rabbits preconditioned 72 h earlier was significantly smaller than that in control rabbits. The activity of lactate dehydrogenase (LDH) and the level of 6-Keto-PGF1alpha in the rabbits preconditioned 72 h earlier were lower than those in control rabbits. The left ventricular systolic pressure (LVSP) and maximal velocity of contraction and relaxation (+/- dP/dtmax) were improved in rabbits preconditioned 72 h earlier. The nNOS-selective inhibitors N-propyl-L-arginine and selective cyclooxygenase-2 (COX-2) inhibitor celecoxib completely blocked the protection of late IP at 72 h, whereas the iNOS selective inhibitor S-methybisothiourea had no effect. In conclusion, the cardioprotection observed in the final stage of late IP (72 hours) is mediated by nNOS or COX-2, but not by iNOS.


Subject(s)
Animals , Male , Rabbits , Cyclooxygenase 2 , Metabolism , Physiology , Ischemic Preconditioning, Myocardial , Myocardial Infarction , Pathology , Myocardial Reperfusion Injury , Metabolism , Nitric Oxide Synthase Type I , Metabolism , Physiology , Random Allocation , Time Factors
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