Insulin and resveratrol act synergistically, preventing cardiac dysfunction in diabetes, but the advantage of resveratrol in diabetics with acute heart attack is antagonized by insulin

• Published in: Free radical biology & medicine 2010-12, Vol.49 (11), p.1710-1721
• Main Authors: Huang, Jiung-Pang, Huang, Shiang-Suo, Deng, Jen-Ying, Chang, Chih-Chun, Day, Yuan-Ji, Hung, Li-Man
• Format: Article
• Language: English
• Subjects: Acute Disease; Animals; Cardiovascular disease; Diabetes; Diabetes Mellitus, Experimental - complications; Diabetic Cardiomyopathies - mortality; Diabetic Cardiomyopathies - physiopathology; Diabetic Cardiomyopathies - prevention & control; Drug Antagonism; Drug Evaluation, Preclinical; Drug Synergism; Free radicals; Heart Failure - drug therapy; Heart Failure - pathology; Hemodynamics - drug effects; Hypoglycemic Agents - administration & dosage; Hypoglycemic Agents - pharmacology; I/R injury; iNOS; Insulin; Insulin - administration & dosage; Insulin - pharmacology; Male; Myocardial Reperfusion Injury - mortality; Myocardial Reperfusion Injury - physiopathology; Myocardial Reperfusion Injury - prevention & control; Nitrotyrosine; Rats; Rats, Sprague-Dawley; Resveratrol; Stilbenes - administration & dosage; Stilbenes - antagonists & inhibitors; Stilbenes - pharmacology; Streptozocin; Vasodilator Agents - administration & dosage; Vasodilator Agents - antagonists & inhibitors; Vasodilator Agents - pharmacology
• ISSN: 0891-5849; 1873-4596
• DOI: 10.1016/j.freeradbiomed.2010.08.032

Resveratrol (RSV), a natural phenolic compound, has been found to display cardiovascular protective and insulin-sensitizing properties. In this study, the effects of RSV and its combination with insulin on mortality, hemodynamics, insulin signaling, and nitrosative stress were compared in streptozotocin (STZ)-induced diabetic rats with or without acute myocardial ischemia/reperfusion (I/R) injury. Under normoxic conditions, cardiac systolic and diastolic functions and insulin-mediated Akt/GLUT4 (glucose transporter 4) activation were impaired in STZ-diabetic rats. The combination of RSV and insulin significantly prevented the above diabetes-associated abnormalities. Notwithstanding that, the diabetic state rendered the animals more susceptible to myocardial I/R injury, and the mortality rate and inducible nitric oxide synthase (iNOS)/nitrotyrosine protein expression and superoxide anion production were also further increased in I/R-injured diabetic hearts. In contrast, RSV treatment alone resulted in a lower mortality rate (from 62.5 to 18%) and better cardiac systolic function than its combination with insulin. RSV also inhibited iNOS/nitrotyrosine protein overexpression and superoxide anion overproduction in I/R-injured diabetic myocardium. Hyperglycemia, impairment of insulin signaling, overexpression of iNOS/nitrotyrosine, and superoxide anion overproduction were markedly rescued by the combination treatment, which did not show an improvement in mortality rate (30%) or cardiac performance over RSV treatment alone. These results indicate that insulin and RSV synergistically prevented cardiac dysfunction in diabetes and this may be in parallel with activation of the insulin-mediated Akt/GLUT4 signaling pathway. Although activation of the protective signal (Akt/GLUT4) and suppression of the adverse markers (iNOS, nitrotyrosine, and superoxide anion) were simultaneously observed in insulin and RSV combination treatment, insulin counteracted the advantage of RSV in diabetics with acute heart attack.