Cardioprotective potential of Punica granatum extract in isoproterenol-induced myocardial infarction in Wistar rats
- 1*,
- 1,
- 2,
- 3
- 1Department of Pharmacology, M. G. V’s Pharmacy College, Panchavati, Nashik, Maharashtra, India.
- 2Clinipath, Computerised Laboratory, 1-Shriram Niketan, Opp. Kulkarni Garden, Sharanpur Road, Nashik, Maharashtra, India.
- 3Pinnacle Biomedical Research Institute, Bhopal-462 003, India.
Published in Journal of Pharmacology and Pharmacotherapeutics
Correspondence: Mahalaxmi Mohan
Department of Pharmacology, M. G. V’s Pharmacy College, Panchavati, Nashik, Maharashtra, India.
Email: mm_nasik@yahoo.co.in
Copyright: © 2010 The Author(s). This is an open access article.
Abstract
Objective: To determine the protective role of Punica granatum L. (Punicaceae) seed juice extract and its butanolic fraction on heart rate, electrocardiographic patterns, vascular reactivity to catecholamines, cardiac marker enzymes, antioxidant enzymes together with morphologic and histopathological changes in isoproterenol-induced myocardial infarction in male Wistar rats. Materials and Methods: The effects of Punica granatum seed juice extract (100 mg/kg, p.o. and 300 mg/kg, p.o.) and butanolic fraction of Punica granatum seed juice extract (100 mg/kg., p.o.) on cardiac parameters were studied. Isoproterenol hydrochloride was used to induce myocardial infarction in Wistar rats. At the end of the experiment, heart rate, ECG, pressure rate index and cardiac marker enzyme levels were assessed. Results: Rats treated with isoproterenol (85 mg/kg, administered subcutaneously twice at an interval of 24 h) showed a significant increase in heart rate, ST elevation in ECG, pressure rate index and a significant increase in the levels of cardiac marker enzymes- lactate dehydrogenase, and creatine kinase in serum. Isoproterenol significantly reduced superoxide dismutase and catalase activity and increased vascular reactivity to various catecholamines. Pretreatment with PJ (100 mg/kg, p.o. and 300 mg/kg, p.o.) and B-PJ (100 mg/kg., p.o.) for a period of 21 days significantly inhibited the effects of ISO on heart rate, PRI, ECG patterns, levels of LDH, CK, SOD, CAT, and vascular reactivity changes. Treatment with PJ (100 mg/kg and 300 mg/kg) and B-PJ (100 mg/kg., p.o.) alone did not alter any of the parameters as compared to vehicle-treated Wistar rats. Punica granatum-treated animals showed a lesser degree of cellular infiltration in histopathological studies. Conclusion: Punica granatum ameliorates cardiotoxic effects of isoproterenol and may be of value in the treatment of MI.
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