Antioxidant activity of Pepticare, a herbomineral formulation, in experimentally induced renal and cardiac damage.

Journal of herbal pharmacotherapy Pub Date : 2006-01-01
Pallavi Anand Bafna, R Balaraman
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Abstract

Pepticare, a herbomineral formulation, was administered orally to rats at the dose levels of 125, 250, 500 and 1000 mg/kg to investigate its effect on isoproterenol-induced myocardial infarction and cisplatin-induced renal damage. The drug reduced the levels of serum creatine kinase (CK), glutamic oxaloacetate transaminase (GOT), lactate dehydrogenase (LDH) and uric acid in isoproterenol-induced cardiac damage. In cisplatin-induced renal damage, Pepticare reduced the serum levels of creatinine, urea, blood urea nitrogen (BUN) and uric acid. It was further found that administration of Pepticare increased the levels of superoxide dismutase (SOD), catalase (CAT), reduced glutathione (GSH), membrane bound enzymes like Ca2+ ATPase, Mg2+ ATPase and Na+ K+ ATPase and decreased lipid peroxidation (MDA) in heart and kidney, respectively. Thus it can be concluded that Pepticare possesses antioxidant activity and protects the heart and kidney from damage caused by isoproterenol and cisplatin, respectively.

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Pepticare,一种草药制剂,在实验诱导的肾脏和心脏损伤中的抗氧化活性。
采用125、250、500、1000 mg/kg给药大鼠,观察其对异丙肾上腺素致心肌梗死和顺铂致肾损害的影响。该药可降低异丙肾上腺素致心脏损伤患者血清肌酸激酶(CK)、谷草酰乙酸转氨酶(GOT)、乳酸脱氢酶(LDH)和尿酸水平。在顺铂引起的肾损害中,Pepticare降低了血清肌酐、尿素、血尿素氮(BUN)和尿酸水平。进一步发现,Pepticare增加了心脏和肾脏中超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、还原性谷胱甘肽(GSH)、Ca2+ atp酶、Mg2+ atp酶和Na+ K+ atp酶等膜结合酶的水平,降低了脂质过氧化(MDA)。由此可见,Pepticare具有抗氧化活性,可保护心脏和肾脏免受异丙肾上腺素和顺铂的损伤。
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