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出 处:《中药药理与临床》2013年第3期46-48,共3页Pharmacology and Clinics of Chinese Materia Medica
摘 要:目的:研究苦参素对大鼠急性酒精性肝损伤的保护作用及作用机制。方法:构建大鼠急性酒精性肝损伤模型,测定造模第3日、第5日血清谷丙转氨酶(ALT)和谷草转氨酶(AST);测定第5日肝组织超氧化物歧化酶(SOD)、丙二醛(MDA)、还原型谷胱甘肽(GSH)和谷胱甘肽过氧化物酶(GSH-Px)的水平;测定肝细胞凋亡程度及肝脏沉默信息调节因子1(Sirt1)的mRNA及蛋白表达。结果:大鼠急性酒精性肝损伤后第3日和第5日血清ALT、AST水平升高;肝组织SOD、GSH、GSH-Px降低,MDA升高;细胞凋亡显著;Sirt1的mRNA和蛋白表达降低。苦参素40 mg/kg组和苦参素80 mg/kg组能不同程度减轻肝损伤,其机制可能与苦参素提高了Sirt1的mRNA和蛋白表达相关。结论:苦参素在大鼠急性酒精性肝损伤中发挥保护作用,其机制可能与提高肝脏Sirt1的mRNA和蛋白表达相关。Objective:To investigate the protective effect of matrine on acute alcoholic liver injury in rats and its mechanism.Methods: Establish the model of acute alcoholic liver injury in rats.The salanine aminotransferase(ALT),aspartate aminotransferase(AST) in the serum,the hepatic superoxide dismutase(SOD),malondialdehyde(MDA),glutathione(GSH),glutathione peroxidase(GSH-Px),the hepatic apoptosis,and silent information regulator factor 1(Sirt1) mRNA and protein expression in the liver were measured.Results: we detected the serum ALT and AST were elevated in rats of acute alcoholic liver injury,together with hepatic SOD,GSH and GSH-PX decreased;MDA and apoptotic positive index increased.Moreover,hepatic Sirt1 mRNA and protein expressions were suppressed.Such damages were alleviated in matrine pretreatment group(40 mg/kg,80 mg/kg),the potential mechanism may be related to Sirt1 mRNA and protein expressions were elevated by matrine pretreatment.Conclusion: Matrine has significant protective effects on acute alcoholic liver injury in rats.The mechanism of its protective effects may relate to its induced property of Sirt1 mRNA and protein.
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