Attenuation of Ischemia/Reperfusion Injury in Rats by the Anti-inflammatory Action of Resveratrol
| Autor: | Samarjit Das, Aldo Bertelli, Dipak K. Das, Nilanjana Maulik, M. Falchi |
|---|---|
| Rok vydání: | 2011 |
| Předmět: |
Male
Myocardial Infarction Ischemia Nitric Oxide Synthase Type II Apoptosis Blood Pressure Myocardial Reperfusion Injury Pharmacology Resveratrol Nitric Oxide Nitric oxide Rats Sprague-Dawley chemistry.chemical_compound Malondialdehyde Stilbenes Drug Discovery In Situ Nick-End Labeling medicine Animals RNA Messenger Cell adhesion Chemistry Anti-Inflammatory Agents Non-Steroidal food and beverages medicine.disease Rats Mechanism of action Biochemistry Enzyme Induction Heart Function Tests medicine.symptom Cell Adhesion Molecules Reperfusion injury Intracellular Leukocyte chemotaxis |
| Zdroj: | Arzneimittelforschung. 56:700-706 |
| ISSN: | 1616-7066 0004-4172 |
| DOI: | 10.1055/s-0031-1296776 |
| Popis: | Resveratrol (trans-3,4',5-trihydroxystilbene, CAS 501-36-0), a natural antioxidant and polyphenol found in grapes and wine, has been found to pharmacologically precondition the heart in nitric oxide (NO)-dependent manner. In the vascular system, NO functions as an endogenous inhibitor of leukocyte chemotaxis, adherence, and activation. The present study was designed to determine if resveratrol, through NO, can block the proadhesive molecules generated in the ischemic reperfused myocardium. Isolated hearts were prepared from properly anesthetized rats, and mounted on a Langendorff apparatus. The hearts were randomly assigned to one of the three groups: (i) control, (ii) resveratrol, and (iii) resveratrol + NG-nitro-L-arginine ethyl ester (L-NAME). The hearts were perfused in the absence (n = 6) or presence of 10 micromol/L resveratrol (n=6) or resveratrol + L-NAME (n = 6) for 15 min. All the hearts were then subjected to 30 min ischemia followed by 2 h of reperfusion. Ventricular function was monitored, infarct size and apoptotic cell death measured, and the proadhesive molecules and malonaldehyde formation determined in the perfusate. Resveratrol significantly improved postischemic ventricular function and reduced myocardial infarct size compared to the non-treated control group. The amount of proadhesive molecules including soluble intracellular adhesion molecule-1 (sICAM-1), endothelial leukocyte adhesion molecule-1 (sE-Selectin) and vascular cell adhesion molecule-1 (sVCAM-1) were each significantly decreased during reperfusion in the resveratrol group. L-NAME, a NO blocker, completely abolished such beneficial effects of resveratrol. The results support an anti-inflammatory action of resveratrol through a NO-dependent mechanism. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|