Protective effects of the SOD-mimetic SC-52608 against ischemia/reperfusion damage in the rabbit isolated heart
| Autor: | U. Ryan, C. S. Schasteen, R. H. Weiss, D. P. Riley, Kenneth S. Kilgore, Benedict R. Lucchesi, C. R. Johnson, Gregory S. Friedrichs |
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| Rok vydání: | 1994 |
| Předmět: |
Intracellular Fluid
Male medicine.medical_specialty Myocardial ischemia Ischemia Myocardial Ischemia Blood Pressure Myocardial Reperfusion Injury Pharmacology Myosins Antioxidants Superoxide dismutase Superoxides Internal medicine Coronary Circulation medicine Organometallic Compounds Animals Molecular Biology Creatine Kinase biology business.industry Experimental model Superoxide Dismutase Myocardium Antibodies Monoclonal Cardiovascular Agents Isolated heart Free Radical Scavengers medicine.disease Isoenzymes Perfusion Microscopy Electron Cardiology biology.protein Potassium Intracellular potassium Creatine kinase Rabbits Cardiology and Cardiovascular Medicine business Reperfusion injury |
| Zdroj: | Journal of molecular and cellular cardiology. 26(8) |
| ISSN: | 0022-2828 |
| Popis: | An experimental model of myocardial ischemia/reperfusion injury was used to assess the cardioprotective effects of SC-52608, a low molecular weight superoxide dismutase mimetic. Langendorff perfused rabbit isolated hearts were subjected to 30 min of global ischemia followed by 45 min of reperfusion. Hearts perfused in the presence of 20 microM SC-52608 exhibited a decrease in the release of creatine kinase and intracellular potassium compared to hearts receiving vehicle (control). A progressive increase in left ventricular end-diastolic pressure developed upon reperfusion in all hearts, but was significantly greater in control hearts when compared to hearts treated with SC-52608 (P0.05). In addition, results obtained with a radiolabeled monoclonal antibody to the intracellular protein myosin, indicate an increased degree of irreversible damage in vehicle-treated hearts. Myocardial protection was not significant in an additional group of hearts treated with 10 microM SC-52608. The hemodynamic, biochemical, morphological, as well as the antimyosin binding data, demonstrate that pretreatment with SC-52608 protects the myocardium from damage associated with global ischemia and reperfusion. The mechanism by which SC-52608 mediates the observed protective effect is most likely related to its ability to scavenge superoxide. |
| Databáze: | OpenAIRE |
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