Histopathological study of erythropoietin protective effect on carbon monoxide-induced cardiotoxicity in rat
نویسندگان
1 Department of Pharmacodynamics and Toxicology, School of Pharmacy, Mashhad University
2 Department of Toxicology and Pharmacology, Faculty of Pharmacy, Kerman University
3 Medical Toxicology Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
4 Department of Pharmacodynamics and Toxicology, School of Pharmacy, Mashhad University
5 Pharmaceutical Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
6 Pharmaciutical Research Center, Institute of Neuropharmacology, Kerman University
7 Department of Pharmacology and Toxicology, Faculty of Pharmacy, University of Ahl Al Bayt, Karbala, Iraq
8 Pharmaceutical Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
doi
10.22038/ijbms.2017.9471چکیده
Objective(s): Cardiotoxicity is one of the major consequences in carbon monoxide poisoning. Following our previous work, in this study we aimed to define the myocardium changes induced by carbon monoxide (CO) intoxication and evaluate erythropoietin (EPO) effect on CO cardiotoxicity in rat. Materials and Methods: Severe carbon monoxide toxicity induced by 3000 ppm CO in Wistar rat. EPO was administrated (5000 IU/Kg, intraperitoneal injection) at the end of CO exposure and then the animals were re-oxygenated with the ambient air. Subsequently heart was removed and assessed by histopathology and electron microscopy examinations. Results: 3000 ppm CO induced significant myocardium injury; multiple foci of necrosis and lymphocyte infiltration compare with the control (P˂0.05). Electron microscopy examination showed myofibril lysis and mitochondrial swelling in myocardium due to 3000 ppm CO poisoning. However EPO administration after CO exposure resulted in significant reduction in cardiomyocytes injury (P˂0.05). Conclusion: Our results represented protective effect of EPO on cardiac injury induced by CO intoxication in rat.