基础医学与临床 ›› 2014, Vol. 34 ›› Issue (10): 1367-1371.

• 研究论文 • 上一篇    下一篇

LPS上调大鼠HIF-1?和GLUT表达及调控糖代谢

严洁萍,俞佳,吴越,吕良忠   

  1. 浙江省人民医院
  • 收稿日期:2014-03-10 修回日期:2014-05-26 出版日期:2014-10-05 发布日期:2014-09-25
  • 通讯作者: 严洁萍 E-mail:pinkieyan@126.com
  • 基金资助:
    克服胃肠吸收屏障的中药复方脂质载体给药系统研究

LPS Up-regulates HIF-1? and GLUT Expressions in Rats

  • Received:2014-03-10 Revised:2014-05-26 Online:2014-10-05 Published:2014-09-25

摘要: 目的 探讨脂多糖(LPS)致大鼠内毒素血症早期,葡萄糖转运体(GLUT)家族在脑、心和肝组织等表达水平及低氧诱导因子-1?(HIF-1?)调控的相关性。方法 雄性SD大鼠分为对照组(腹腔注射0.9%氯化钠注射液)和给药组(腹腔注射2 mg/kg LPS),每组6只。测定给药后0 ~ 24 h体温。ELISA法检测血清IL-1?水平。RT-PCR法测定GLUT家族mRNA表达。Western blot法检测GLUT1和HIF-1?蛋白表达。结果 在大鼠脑、心及肝等组织中,GLUT1和GLUT4均有表达;GLUT2在脑和肝组织中有表达;GLUT3仅在脑组织特异性表达。LPS作用24 h可引起大鼠体温升高,血清IL-1?水平上调(P<0.05)。LPS可上调脑组织GLUT1 mRNA水平和蛋白翻译水平(P<0.01);同时LPS可促脑组织HIF-1?蛋白稳定表达(P<0.001)。结论LPS促大鼠HIF-1?稳定表达,上调GLUT1表达及调控糖代谢。

关键词: 葡萄糖转运体, 低氧诱导因子-1, 脂多糖, SD大鼠

Abstract: Objective Characterization of glucose transporter (GLUT) family and potential role of HIF-1? in lipopolysacchride (LPS)-induced endotoxemic rats was investigated, and this information helps to understand GLUT family in endotoxemic rats. Methods SD rats were treated with a single dose injection (i.p.) of LPS (2 mg/kg), and rats in control group were given equal amount of NaCl (0.9%) (n=6). The body temperature was detected after LPS treatment for 0 ~ 24 h. IL-1? release was evaluated by ELISA assay. GLUT mRNA expression was determined by RT-PCT assay. HIF-1? and GLUT1 protein expression were examined. Results LPS increased rats’ body temperature and IL-1? release in serum(P<0.05). GLUT1 and GLUT4 expressed in brain, heart and liver. GLUT2 expressed in brain and liver. GLUT3 mainly expressed in brain. LPS increased GLUT1 mRNA and protein expression in the brain (P<0.01). HIF-1? kept stability in the brain of LPS-challenged rats (P<0.001). Conclusion LPS induced GLUT1 overexpression and HIF-1? stability in the brain of the endotoxemic rats. It indicated that HIF-1?-induced GLUT1 upregulation might be a potential way to regulate glucose metabolism in LPS-challenged rats.

Key words: glucose transporter, hypoxia-inducible factor-1, lipopolysacchride, SD rats

中图分类号: