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Am J Physiol Heart Circ Physiol 282: H1953-H1960, 2002; doi:10.1152/ajpheart.01045.2001
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Vol. 282, Issue 6, H1953-H1960, June 2002

Role of delta -opioid receptor agonists on infarct size reduction in swine

Daniel C. Sigg1,2, James A. Coles Jr.1,3, Peter R. Oeltgen4, and Paul A. Iaizzo1,2,3

Departments of 1 Anesthesiology and 2 Physiology and the 3 Biomedical Engineering Institute, University of Minnesota, Minneapolis, Minnesota 55455; and 4 Department of Pathology, University of Kentucky, Lexington, Kentucky 40511

Opioids are involved in cardiac ischemic preconditioning. Important species differences in cellular signaling mechanisms, antiarrhythmic, and antistunning effects have been described. The role of the delta -opioid receptor activation in swine remains unknown. Forty minutes before a 45-min occlusion and 180-min reperfusion of the left anterior descending coronary artery, open-chest, pentobarbital-anesthetized swine received either 1) saline (controls); 2) [D-Ala2,D-Leu5]enkephalin (DADLE); 3) [D-Pen2,5]enkephalin (DPDPE); 4) deltorphin-D, a novel delta 2-opioid agonist; or 5) ischemic preconditioning (IP). Assessed were 1) infarct size to area at risk (IS, triphenyltetrazolium staining), 2) regional and global myocardial function (sonomicrometry, ventricular pressure catheters), and 3) arrhythmias (electrocardiogram analyses). It was found that DPDPE and deltorphin-D pretreatment reduced IS from 64.7 ± 5 to 36.5 ± 6% and 27.4 ± 11% (P < 0.01), respectively, whereas DADLE had no effect (66.8 ± 3%). Both IP and DADLE had a proarrhythmic effect (P < 0.01). However, no differences in global or regional myocardial function or arrhythmia scores were observed between groups. This suggests that delta -receptor-specific opioids provide cardioprotection in swine.

cardioprotection; myocardial ischemia; regional myocardial function; arrhythmia; kappa -opioid receptor


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