Key result
Sesamol attenuates isoproterenol-induced myocardial injury and oxidative stress in rats, most effectively at 50 mg/kg.
This study was designed to investigate the cardioprotective effect of sesamol on isoproterenol (ISO)-induced myocardial infarction in adult male albino Wistar rats. The heart damage induced by ISO was indicated by elevated levels of the marker enzymes such as alanine aminotransferase (ALT), aspartate aminotransferase (AST), lactate dehydrogenase (LDH), creatine kinase (CK), creatine kinase-MB (CK-MB) and the levels of troponin T and I in the plasma. In addition, lipid peroxidative markers such as thiobarbituric acid reactive substances (TBARS), conjugated dienes (CD) and lipid hydroperoxides (LHP) significantly increased in the plasma and heart. Activities of superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), glutathione-S-transferase (GST) and glutathione reductase (GR) significantly decreased in the heart and (non-enzymic antioxidants) vitamin C, vitamin E and reduced glutathione (GSH)) levels significantly decreased in the plasma and heart in ISO-rats. Histopathological observations correlated with the biochemical parameters. Administration of sesamol at different doses 50, 100 and 200 mg/kg body weight intraperitoneally for 7 days prevented the above changes and improved towards normality; the 50 mg dose was more effective than the other two doses.
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Vennila et al. (2010) studied Isoproterenol-induced myocardial infarction. Sesamol vs. Untreated isoproterenol-induced myocardial infarction control rats was evaluated on Cardiac marker enzymes (ALT, AST, LDH, CK, CK-MB), troponin T and I, lipid peroxidation markers (TBARS, CD, LHP), antioxidant levels (SOD, CAT, GPx, GST, GR, vitamin C, vitamin E, GSH), and histopathology. Sesamol (50, 100, and 200 mg/kg for 7 days, with 50 mg/kg most effective) prevented isoproterenol-induced cardiac marker elevations, lipid peroxidation, and antioxidant depletion in rats.
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