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首页|期刊导航|世界中医药|木犀草素改善高脂诱导的 ApoE-/-小鼠非酒精性脂肪肝及动脉粥样硬化作用研究

木犀草素改善高脂诱导的 ApoE-/-小鼠非酒精性脂肪肝及动脉粥样硬化作用研究

罗云 卢珊 周平 孙桂波 孙晓波

世界中医药Issue(8):1144-1147,1151,5.
世界中医药Issue(8):1144-1147,1151,5.DOI:10.3969/j.issn.1673-7202.2015.08.004

木犀草素改善高脂诱导的 ApoE-/-小鼠非酒精性脂肪肝及动脉粥样硬化作用研究

Effects of Luteolin on High Fat Diet-induced ApoE-/-mice With Non-alcoholic Steatohepatitis and Atherosclerosis

罗云 1卢珊 1周平 2孙桂波 1孙晓波1

作者信息

  • 1. 中国医学科学院北京协和医学院药用植物研究所药理毒理中心,北京,100193
  • 2. 哈尔滨商业大学生命科学与环境科学研究中心,哈尔滨,150076
  • 折叠

摘要

Abstract

Objective:This study was to explore the possible effects of luteolin on ApoE-/-mice with non-alcoholic steatohepatitis induced by high fat diet as well as the efficacy on atherosclerosis.Methods:The model was induced by high fat diet,and luteolin were administered by gastric perfusion at 70 and 1 40 mg/kg qd for 1 2 weeks.The serum level of superoxide dismutase(SOD), malondialdehyde(MDA),glutathion peroxidase(GSH-Px)were measured.The contents of alanine transaminase(ALT),aspartate aminotransferase(AST)were measured in liver tissue of grout.The pathological changes of liver tissue were examined by HE stai-ning and the lipid accumulation in the liver and aortic root was tested by oil red O staining.The apoptotic hepatocytes were detec-ted by TUNEL assay and the expression levels of Bcl-2 and caspase-3 were observed by immunohistochemisty.Results:The results showed that Luteolin(70,1 40 mg/kg)improved the liver function significantly through reducing the level of ALT,AST,and in-creasing the content of SOD,GSH-Px and Bcl-2 while reducing the content of MDA,lipid accumulation,hepatic steatosis, TUNEL-positive cells and the expression of caspase-3.Conclusion:The results suggest that Luteolin may inhibit the liver injury and atherosclerosis induced by high fat diet by decreasing the oxidative stress.

关键词

木犀草素/非酒精性脂肪肝/动脉粥样硬化/氧化损伤/ApoE-/-小鼠

Key words

Luteolin/Non-alcoholic steatohepatitis/Atherosclerosis/Oxidative injury/ApoE-/-mice

分类

医药卫生

引用本文复制引用

罗云,卢珊,周平,孙桂波,孙晓波..木犀草素改善高脂诱导的 ApoE-/-小鼠非酒精性脂肪肝及动脉粥样硬化作用研究[J].世界中医药,2015,(8):1144-1147,1151,5.

基金项目

国家自然科学基金项目(编号81374010);国家科技重大专项课题,重大新药创制基金 ()

世界中医药

OACHSSCDCSTPCD

1673-7202

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