基础医学与临床 ›› 2009, Vol. 29 ›› Issue (1): 64-68.

• 研究论文 • 上一篇    下一篇

二甲双胍抑制OLETF大鼠肝组织TNF-α表达

董爱梅 郭晓蕙 王薇   

  1. 北京大学第一医院内分泌科 北京大学第一医院内分泌科 北京大学第一医院内分泌科
  • 收稿日期:2007-08-30 修回日期:2008-06-17 出版日期:2009-01-25 发布日期:2009-01-25
  • 通讯作者: 董爱梅

The inhibitory effect of Metformin on TNF-α Expression in hepatic tissue of OLETF Rats

Ai-mei DONG, Xiao-hui GUO, Wei WANG   

  1. Department of Endocrinology, the First Hospital, Peking University Department of Endocrinology, the First Hospital, Peking University Department of Endocrinology, the First Hospital, Peking University
  • Received:2007-08-30 Revised:2008-06-17 Online:2009-01-25 Published:2009-01-25
  • Contact: Ai-mei DONG,

摘要: 目的 观察自发胰岛素抵抗的OLETF大鼠糖脂代谢异常的同时肝组织肿瘤坏死因子-α(TNF-α)表达水平的变化以及二甲双胍治疗对TNF-α表达水平的影响。方法 以野生型的LETO大鼠作为对照(LETO组),OLETF大鼠分为OLETF组和OLETF/M组(二甲双胍 100mg/kg·日)。治疗22周,测定肝组织三酰甘油含量,用Western blot方法测定肝组织TNF-α蛋白表达水平,用定量PCR方法测定TNF-αmRNA的表达水平。结果 与LETO组大鼠相比OLETF组大鼠空腹血糖、胰岛素以及三酰甘油、游离脂肪酸的水平显著升高,肝组织三酰甘油含量增加。同时,OLETF组大鼠肝组织TNF-α蛋白表达水平为LETO组大鼠的1.57倍(P<0.05), TNF-αmRNA表达水平是LETO组的1.67倍(P<0.05)。经二甲双胍治疗,OLETF/M组大鼠的空腹血糖、胰岛素、游离脂肪酸及肝组织三酰甘油含量明显下降。OLETF/M组大鼠TNF-α的表达水平也显著受抑,其中蛋白表达水平较OLETF组下调59%(P<0.05)、mRNA水平下调45%(P<0.05)。结论 抑制肝脏TNF-α表达是二甲双胍发挥改善胰岛素敏感性及肝脏脂肪变作用的重要纽带。

关键词: 二甲双胍, TNF-α, 胰岛素抵抗, 脂肪肝

Abstract: Objective To investigate the TNF-α expression in hepatic tissue of Otsuka Long-Evans Tokushima Fatty (OLETF) rats (an insulin resistance model) with abnormalities of glucose-lipid metabolism and effect of metformin on TNF-α expression. Methods OLETF rats were assigned to two groups randomly (OLETF and OLETF/M).The OLETF/M group was treated with metformin (100 mg/(kg·d)), the OLETF group and age-matched LETO (nondiabetic Long-Evans Tokushima Otsuka rats) group was fed with placebo. After 22 weeks of treatment, we analyzed rats hepatic triglyceride levels and measured expression of TNF-αby western-blot (protein) and quantitative RT-PCR(mRNA). Results After 22 weeks of treatment, the levels of fasting glucose, insulin, triglyceride, free fatty acids (FFA) and hepatic triglyceride were increased significantly in OLETF group compared with LETO group. Western-blot method showed upregulated expression of TNF-α protein in OLETF group (1.57-fold vs LETO group, P <0.05). On the mRNA level, expression of TNF-α were also elevated significantly in OLETF group (1.67-fold vs LETO group, P <0.05). Metformin reduced levels of fasting glucose, insulin, FFA and hepatic triglyceride significantly in OLETF/M group. After treatment of metformin, the expressions of TNF-α protein and mRNA in hepatic tissue downregulated (protein: 59%, P<0.05 and mRNA: 45%, P<0.05)in OLETF/M group. Conclusion The therapeutic effects of metformin on insulin resistance and fatty liver disease were associated with the significant suppression of TNF-α expression in hepatic tissue.

Key words: metformin, TNF-α, insulin resistance, fatty liver disease