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首页|期刊导航|中国药理学通报|氧化苦参碱对高脂诱导胰岛素抵抗ApoE -/-小鼠肝脏脂代谢相关基因的影响

氧化苦参碱对高脂诱导胰岛素抵抗ApoE -/-小鼠肝脏脂代谢相关基因的影响

王杏 王超 宋光耀 费雯婕 刘小娜 张哲 马欢

中国药理学通报Issue(12):1688-1692,5.
中国药理学通报Issue(12):1688-1692,5.DOI:10.3969/j.issn.1001-1978.2015.12.012

氧化苦参碱对高脂诱导胰岛素抵抗ApoE -/-小鼠肝脏脂代谢相关基因的影响

Effect of oxymatrine on lipid metabolism regulated genes in liver of fat-induced insulin resistance in ApoE -/-mice

王杏 1王超 1宋光耀 2费雯婕 2刘小娜 2张哲 1马欢1

作者信息

  • 1. 河北省人民医院 1.老年医学重点实验室
  • 2. 内分泌科,河北 石家庄 050051
  • 折叠

摘要

Abstract

Aim To investigate the effect of oxymatrine on lipid metabolism regulated genes in liver in fat-in-duced insulin resistance in ApoE -/- mice.Methods Seventeen C57BL/6J male mice were selected in normal control group.Sixty-eight ApoE -/- mice with high fat diet for 1 6 weeks,were randomly divided into model group,oxymatrine low,middle and high dose groups.Then they were gavaged for 8 weeks.Body weight and general biochemical indicators were deter-mined in mice.The mRNA and protein expression lev-els of LPL,FAT/CD36,CPT1 ,UCP2,SREBP-1 c,FAS and ACC were examined by real-time PCR and West-ern blot in the liver.Results Compared with model group,oxymatrine reduced body weight(BW),fasting <br> blood glucose (FBG),cholesterol (TC ),triglyceride (TG),free fatty acids(FFA),fasting plasma insulin (FINS)and insulin resistance index(HOMA-IR)(P <0.05),while improved glucose infusion rate (GIR). Oxymatrine down-regulated the mRNA and protein ex-pression of LPL,FAT/CD36,UCP2,SREBP-1 c,FAS and ACC(P <0.05),and up-regulated the mRNA and protein expression of CPT1 in varying degrees (P <0.05).Conclusion Oxymatrine can regulate the ex-pression of lipid metabolism regulated genes in liver and improve insulin resistance in ApoE -/- mice in-duced by high fat diet.

关键词

氧化苦参碱/高脂/ApoE -/-小鼠/胰岛素抵抗/脂代谢/肝脏

Key words

oxymatrine/high fat diet/ApoE -/- mice/insulin resistance/lipid metabolism/liver

分类

医药卫生

引用本文复制引用

王杏,王超,宋光耀,费雯婕,刘小娜,张哲,马欢..氧化苦参碱对高脂诱导胰岛素抵抗ApoE -/-小鼠肝脏脂代谢相关基因的影响[J].中国药理学通报,2015,(12):1688-1692,5.

基金项目

国家自然科学基金资助项目(No 81370900);河北省重大医学科研项目 ()

中国药理学通报

OA北大核心CSCDCSTPCD

1001-1978

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