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Opioid system and cardiac resistance to ischemic and reperfusion injuries
Authors:Lishmanov Iu B  Maslov L N  Tam S V  Bogomaz S A
Institution:Research Institute of Cardiology, Siberian Branch of the Russian Acad. Med. Sci., Tomsk.
Abstract:In vivo pre-treatment with the opioid receptor antagonist D,L-naloxone completely eliminated the reperfusion-induced creatine kinase (CK) leakage from the rat isolated perfused haert. The inactive isomer L-naloxone decreased the CK release by half. The (-antagonist ICI 174,864 and k-antagonist nor-binanltorphimine exerted a weaker protective effect. The (-antagonist DAMGO, the (2-agonist DSLET, the k1-agonist spiradolin, or the sigma-agonist (+)-SKF 10047, improved myocardial cell viability after ischemia/reperfusion.
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