Rozario R J, Akhter N, Bhuiyan N I, Alom M M
Department of Pharmacology, Shaheed Monsur Ali Medical College, Uttara, Dhaka, Bangladesh.
Mymensingh Med J. 2011 Jul;20(3):472-7.
This study was done to investigate the antioxidant effect of valsartan, an AT1 receptor blocker, when administered in experimental model of myocardial infarction (MI). MI was induced in rats by administration of adrenaline at a dose of 2 mg/kg body weight subcutaneously two injections 24 hrs apart and was assessed by significant elevation of marker enzymes (CK-MB and AST). Valsartan (30 mg/kg body weight) was administered through intragastric tube daily for 2 weeks in both pre- and post- MI groups. Oxidative stress was assessed by the activities of malondialdehyde (MDA) level and reduced glutathione (GSH) level in erythrocytes. In both treated groups, valsartan caused significant recovery of the biochemical markers, GSH and MDA level. These findings suggest that pre- and post-treatment with valsartan had an anti-oxidant effect in patients who are at risk of acute myocardial infarction.
本研究旨在探讨血管紧张素Ⅱ 1型受体(AT1)阻滞剂缬沙坦在心肌梗死(MI)实验模型中给药时的抗氧化作用。通过皮下注射剂量为2mg/kg体重的肾上腺素诱导大鼠心肌梗死,每隔24小时注射一次,共注射两次,并通过标记酶(CK-MB和AST)的显著升高来评估。在心肌梗死前和心肌梗死后两组中,每天通过胃管给予缬沙坦(30mg/kg体重),持续2周。通过红细胞中丙二醛(MDA)水平和还原型谷胱甘肽(GSH)水平的活性评估氧化应激。在两个治疗组中,缬沙坦均使生化标志物、GSH和MDA水平显著恢复。这些发现表明,缬沙坦治疗前和治疗后对有急性心肌梗死风险的患者具有抗氧化作用。