基础医学与临床 ›› 2012, Vol. 32 ›› Issue (10): 1224-1226.

• 研究短文 • 上一篇    下一篇

瘦素及I和III型胶原蛋白在肝纤维化大鼠肝组织中的变化

朱净,潘亮,许晶,陆静娴,黄华,陆翠华   

  1. 南通大学附属医院
  • 收稿日期:2012-02-16 修回日期:2012-03-30 出版日期:2012-10-05 发布日期:2012-09-28
  • 通讯作者: 陆翠华 E-mail:lch670608@sina.com
  • 基金资助:
    南通市社会发展计划基金

Protein and gene dynamic expressions of leptin, collagen I and collagen III in the tissues of hepatic fibrosis model

  • Received:2012-02-16 Revised:2012-03-30 Online:2012-10-05 Published:2012-09-28

摘要: 摘要: 目的 研究瘦素(Leptin)及I、 III型胶原蛋白及基因在肝纤维化模型组织中的动态表达水平。方法 四氯化碳(CCl4)皮下注射法制备肝纤维化模型,分别以Western blot及RT-PCR法检测Leptin及I、 III型胶原蛋白及基因在肝纤维化组织中的动态表达。结果 Leptin以及I、 III型胶原蛋白及基因在正常对照组肝脏中均有微量表达,CCl4注射2周后,三者的表达均开始增强,随着纤维化发展呈梯度增加。其mRNA表达水平在模型组明显高于正常组 (P<0.05);在肝纤维化过程中,Leptin与I型胶原(r=0.595,P=0.017)及Leptin与III型胶原(r=0.478,P=0.011) 的动态改变呈显著正相关。结论 Leptin的表达随着纤维化的程度加重而逐步增强,在肝纤维化过程中,Leptin可能参与了细胞外基质成分(ECM)的合成与降解。

关键词: 瘦素, 肝纤维化, I型胶原, III型胶原

Abstract: Abstract: Objective To investigate protein and gene dynamic expressions of leptin, collagen I and collagen III in the tissues of hepatic fibrosis model. Methods Liver fibrosis models of rats were made by hypodermic injection with 60% CCl4. The protein and gene expressions of leptin, collagen I and collagen III were assayed by Western blot and reverse transcription polymerase chain reaction(RT-PCR), respectively. Results The protein and gene expressions of leptin, collagen I and collagen III were slight in normal liver tissues. In the model groups, the expressions began to increase progressively at the end of the 2nd week after injection with CCl4. The mRNA expression levels of leptin, collagen I and collagen III in the model groups were higher than that in the control group (P<0.05), and there were closely positive correlation between leptin and collagen I(r=0.595, P=0.017), collagen III (r=0.478, P=0.011).Conclusion In the process of hepatic fibrosis induced by CCl4 injection in rats, expression of leptin and collagen I, III are increased with the development of hepatic fibrosis. Leptin probably participate the synthesis and degradation of extracellular matrix in hepatic fibrosis.

Key words: Hepatic fibrosis, Leptin, Collagen I, Collagen III