Ojha Shreesh, Bharti Saurabh, Golechha Mahaveer, Sharma Ashok K, Rani Neha, Kumari Santosh, Arya Dharamvir Singh
Department of Pharmacology, All India Institute of Medical Sciences, New Delhi-1 10029, India.
Acta Pol Pharm. 2012 Mar-Apr;69(2):269-78.
Present study evaluated the cardioprotective effect of Andrographis paniculata (100, 200 or 400 mg/kg) against isoproterenol (85 mg/kg, b.w.)-induced cardiotoxicity referred as myocardial infarction in rats. Isoproterenol significantly (p < 0.05) decreased mean arterial pressure, heart rate, contractility and relaxation and increased left ventricular end diastolic pressure. Isoproterenol also significantly (p < 0.05) decreased antioxidants, superoxide dismutase, catalase, glutathione peroxidase, glutathione and increased leakage of cardiac injury markers; creatine phosphokinase-MB isoenzyme, lactate dehydrogenase concomitant to increased lipid peroxidation and histopathological perturbations. However, pretreatment with A. paniculata favorably restored hemodynamic parameters and left ventricular function and significantly (p < 0.05) prevented the depletion of endogenous antioxidants and myocyte marker enzymes as well as inhibited lipid peroxidation. Significant (p < 0.05) reversal of almost all the hemodynamic, biochemical and histopathological parameters by A. paniculata pretreatment in isoproterenol-induced cardiotoxicity depicted the cardioprotective effect of A. paniculata. Results showed that A. paniculata protected heart against cardiotoxic effects of isoproterenol by boosting endogenous antioxidant network, restoring ventricular function and maintaining structural integrity of heart.
本研究评估了穿心莲(100、200或400毫克/千克)对异丙肾上腺素(85毫克/千克,体重)诱导的大鼠心脏毒性(即心肌梗死)的心脏保护作用。异丙肾上腺素显著(p < 0.05)降低平均动脉压、心率、收缩性和舒张性,并增加左心室舒张末期压力。异丙肾上腺素还显著(p < 0.05)降低抗氧化剂、超氧化物歧化酶、过氧化氢酶、谷胱甘肽过氧化物酶、谷胱甘肽水平,并增加心脏损伤标志物的泄漏;肌酸磷酸激酶-MB同工酶、乳酸脱氢酶,同时伴随着脂质过氧化和组织病理学改变的增加。然而,穿心莲预处理能有利地恢复血流动力学参数和左心室功能,并显著(p < 0.05)防止内源性抗氧化剂和心肌细胞标志物酶的消耗,以及抑制脂质过氧化。穿心莲预处理对异丙肾上腺素诱导的心脏毒性中几乎所有血流动力学、生化和组织病理学参数的显著(p < 0.05)逆转表明了穿心莲的心脏保护作用。结果表明,穿心莲通过增强内源性抗氧化网络、恢复心室功能和维持心脏结构完整性来保护心脏免受异丙肾上腺素的心脏毒性作用。