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肝细胞生长因子对小鼠实验性肠炎P-选择素表达的影响

殷瓅 陆允敏 金湧 陈维雄 朱金水 陈尼维

河北医学2013,Vol.19Issue(4):503-507,5.
河北医学2013,Vol.19Issue(4):503-507,5.DOI:10.3969/j.issn.1006-6233.2013.04.009

肝细胞生长因子对小鼠实验性肠炎P-选择素表达的影响

Influence of Hepatocyte Growth Factor on P-selectin in Experimental Colitis of Mice

殷瓅 1陆允敏 1金湧 1陈维雄 1朱金水 1陈尼维1

作者信息

  • 1. 上海交通大学附属第六人民医院消化内科,上海,200233
  • 折叠

摘要

Abstract

Objective: To investigate the influence of hepatocyte growth factor on P-selectin in experimental colitis of mice, and the potential mechanism of HGF. Method: Sixty mice were randomized into 6 groups:normal group,model group,normal saline treated group( NS ),HGF treated group( HGF ),SASP treated group and HGF and SASP treated group. Except the mice in normal group, all mice were induced by ox-azolone enema. NS was intraperitoneally injected in the mice of NS group( 0. lmL · body-1 · d-1 )after enema . HGF was intraperitoneally injected in the mice of HGF group( 100ug · body'1 · d-1 )after enema. SASP was given by gavage in the mice of SASP group( 200mg · kg-1 · d-1 ) after enema. The mice of HGF and SASP group were treated with both HGF and SASP. All mice were sacrificed at 13th day. Gene expression of P-selectin were detected by fluorescence quantitative PCR( FQ-PCR ). Result: The expression of P-selectin mRNA in model group and NS group were higher than those in normal group( P<0. 01 ). HGF group,SASP group and HGF&SASP group were lower than those in model group and NS group( P<0. 01 ). HGF group and HGF&SASP group were no statistical significance with normal group( P >0. 05 ). SASP group was lower than in normal group( P<0. 05 ), There was no statistical significance between HGF group, SASP group and HGF&SASP group( P >0. 05 ). Conclusion: The results indicate that expression of P-selectin is increased in oxazolone-induced colitis and can be inhibited by HGF.

关键词

肝细胞生长因子/噁唑酮/P-选择素/结肠炎

Key words

Hepatocyte growth factor/ Oxazolone/ P-selectin/ Colitis

引用本文复制引用

殷瓅 ,陆允敏,金湧,陈维雄,朱金水,陈尼维..肝细胞生长因子对小鼠实验性肠炎P-选择素表达的影响[J].河北医学,2013,19(4):503-507,5.

河北医学

OACSTPCD

1006-6233

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