Protective role of Ascidia sydneiensis Stimpson, 1855 on cardiac enzyme biochemistry and histopathology in isoproterenol - induced myocardial ischemia

C. Packiam, R. Margret, V. Meenakshi
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Abstract

Myocardial ischemia refers to the condition in which a portion of a heart is starved of oxygen and nutrients as a result of sudden block i the coronary arteries. It may be caused by chemotherapy, complications from anorexia nervosa , adverse effects of heavy metals intake and an incorrectly administered drug.The aim of the study is to investigate the protective role of Ascidia sydneiensis in isoproterenol - induced myocardial ischemia in rats. The extract was administered at a dose of 50, 100 and 150 mg/kg bw i.g.c for 28 days. The animals of ISO control and Ascidia sydneiensis pretreated groups were given isoproterenol (150 mg/kg bw) at an interval of 24 hours on 29 th and 30 th day of the experiment. Biochemical parameters like LDH, AST, ALT in serum and lipid peroxidation marker enzyme - MDA in both serum and tissue; enzymatic and non-enzymatic myocardial antioxidant enzymes - SOD, CAT, GPx in heart tissue and GSH in both serum and tissue were analysed following standard procedures. Histopathological architecture of cardiac muscle was also studied. A significant increase in the level of LDH, AST, ALT in the serum and lipid peroxidation marker enzyme - MDA in serum and heart tissue and decrease in the enzymatic and non-enzymatic antioxidant enzymes - SOD, CAT, GPx in heart tissue and GSH in both serum and tissue were noted in ISO treated groups. In the pretreated groups all the above parameters were normal. Restoration of enzyme level observed in the co-treated groups indicate that the extract has protective role in ISO - induced myocardial ischemia. Histopathological studies also confirmed the protective nature of the extract on heart tissue. Based on present findings, it is concluded that Ascidia sydneiensis may be a potential and therapeutic agent against the oxidative stress associated ischemic heart disease owing to antioxidant and antiperoxidative activity.
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悉尼海鞘1855对异丙肾上腺素诱导心肌缺血心肌酶生化和组织病理学的保护作用
心肌缺血是指心脏的一部分由于冠状动脉突然阻塞而缺氧和缺乏营养的情况。它可能是由化疗、神经性厌食症并发症、重金属摄入的不良影响和用药不当引起的。本研究旨在探讨悉尼海鞘对异丙肾上腺素所致大鼠心肌缺血的保护作用。以50、100和150 mg/kg bw .g.c的剂量给药28天。ISO对照组和悉尼海鞘预处理组在试验第29天和第30天每隔24小时给予异丙肾上腺素150 mg/kg bw。血清中LDH、AST、ALT等生化指标,血清和组织中脂质过氧化标记酶- MDA等生化指标;按照标准程序分析心肌酶和非酶抗氧化酶——心脏组织中SOD、CAT、GPx和血清和组织中GSH。并对心肌组织病理结构进行了研究。异黄酮处理组大鼠血清中LDH、AST、ALT水平显著升高,血清和心脏组织中脂质过氧化标记酶- MDA水平显著升高,心脏组织中酶和非酶抗氧化酶- SOD、CAT、GPx和血清和组织中GSH水平显著降低。预处理组以上各项指标均正常。共处理组酶水平的恢复表明提取物对异源性心肌缺血有保护作用。组织病理学研究也证实了提取物对心脏组织的保护作用。综上所述,悉尼海鞘具有抗氧化和抗过氧化活性,可能是抗氧化应激相关缺血性心脏病的潜在治疗药物。
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