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梅花钻对乙醇引起小鼠肝损伤的保护作用
引用本文:韦健全,罗莹,薛强,潘勇,郑子敏.梅花钻对乙醇引起小鼠肝损伤的保护作用[J].中国实验方剂学杂志,2011,17(13):167-169.
作者姓名:韦健全  罗莹  薛强  潘勇  郑子敏
作者单位:右江民族医学院药理学教研室,广西百色,533000
基金项目:广西壮族自治区教育厅立项课题(桂教科研【2006】26号,右医科字【2007】2号)
摘    要:目的:研究梅花钻对乙醇引起肝损伤的保护作用。方法:将昆明种小鼠分为正常对照组、乙醇模型组、梅花钻(33.40,16.70,8.35 g·kg-1)剂量组,观察各组小鼠血清的丙氨酸转氨酶(ALT)、天冬氨酸转氨酶(AST)、谷胱甘肽S-转移酶(GST)、超氧化物歧化酶(SOD)活性和肝匀浆中的丙二醛(MDA)、甘油三酯(TG)的含量,评价梅花钻对肝损伤的保护作用。结果:梅花钻高、中剂量组与乙醇模型组比较,ALT,AST,GST,MDA,TG降低(P<0.05或P<0.01),SOD明显升高(P<0.01)。结论:梅花钻对小鼠乙醇引起的肝损伤有保护作用。

关 键 词:梅花钻  乙醇  肝损伤  谷胱甘肽S-转移酶  丙二醛
收稿时间:2010/12/30 0:00:00

Protective Effect of Kadsura heteroclite on Ethanol-induced Hepatotoxicity in Mice
WEI Jian-quan,LUO Ying,XUE Qiang,PAN Yong and ZHENG Zi-min.Protective Effect of Kadsura heteroclite on Ethanol-induced Hepatotoxicity in Mice[J].China Journal of Experimental Traditional Medical Formulae,2011,17(13):167-169.
Authors:WEI Jian-quan  LUO Ying  XUE Qiang  PAN Yong and ZHENG Zi-min
Institution:Department of Pharmacology, Youjiang Medical College for Nationalities, Baise 533000, China;Department of Pharmacology, Youjiang Medical College for Nationalities, Baise 533000, China;Department of Pharmacology, Youjiang Medical College for Nationalities, Baise 533000, China;Department of Pharmacology, Youjiang Medical College for Nationalities, Baise 533000, China;Department of Pharmacology, Youjiang Medical College for Nationalities, Baise 533000, China
Abstract:Objective: To study the protective effect of Kadsura heteroclita(Roxb)Craib(KHC)on ethanol-induced hepatotoxicity in mice. Method: Mice were randomly divided into 5 groups to set up the model of hepatotoxicity by ethanol in mice:the normal,the ethanol model and 3 groups of KHC(33.40,16.70,8.35 g ·kg-1).The activities of alanine transaminase(ALT),aspartate transaminase(AST),glutathione s-transferase(GST),superoxide dismutase(SOD)in serum and the contents of malondialdehyde(MDA),triglyceride(TG)in liver were measured. Result: KHC(33.40,16.70 g ·kg-1,qd×7)could reverse the activities of serum ALT,AST,GST,SOD and could decrease the contents of MDA,TG in liver. Conclusion: KHC showed effective protection on ethanol-induced hepatotoxicity.
Keywords:Kadsura heteroclita  ethanol  hepatotoxicity  glutathione s-transferase  malondialdehyde
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