摘要
目的通过TREM-1基因在重症急性胰腺炎大鼠胰腺、肺组织中的基因表达,探讨TREM。1基因在重症急性胰腺炎发病机制中的作用,进而为治疗重症急性胰腺炎提供新的分子靶点。方法健康雄性Wistar大鼠30只,完全随机分为两组,每组15只。A组:正常组;B组:重症急性胰腺炎组;用5%牛黄胆酸钠逆行胰胆管注射制作重症急性胰腺炎模型。结果TREM-1相对表达量比较:Real—time PCR进行相对定量检测大鼠胰腺、肺组织中TREM-1的相对表达量,B组胰腺、肺两个组织中TREM-1 mRNA相对含量的在6h、12h、24h相应时间点相比明显高于A组,差异有显著性统计学意义(P〈0.05),且随时间变化逐渐升高;且与胰腺病理变化呈正相关。结论重症急性胰腺炎时,TREM-1的相对表达量在大鼠胰腺、肺组织中的明显表达,更能加重胰腺损伤及全身炎症反应综合征。
Objective Through detecting the expression of triggering receptor expressed on myeloid cells-1 (TREM- 1 ) in pancreas and lung of rats with severe acute pancreatitis, to approach the role of TREM- 1 in severe actute pancreatitis pathogenesis, and provid a new molecular target for SAP. Methods Thirty healthy male Wistar rat were randomly divided into two groups: control group( group A) , n = 15 ;severe acute pancreatitis group (group B) , n = 15. The model of severe acute pancreatitis of rats was induced by retrograde injection of 5 % sodium taurocholate into the pancreatic duct. Results TREM- 1 in pancreatic tissues and lung tissues was significantly higher in group B than group A in three time points ( 6 h, 12 h, 24 h) and had significant changes ( P 〈 0.05 ), and had a positive correlation with pancreatic pathology. Conclusion TREM-1 was significantly expressed in severe acute pancreatitis, and aggravated pancreas damage and systemic inflammatory response syndrome.
出处
《国际外科学杂志》
2012年第10期662-665,F0003,共5页
International Journal of Surgery
基金
河北省卫生厅重点课题冀卫科教[2009]30号(No.20090562)
关键词
髓样细胞触发性受体-1
重症急性胰腺炎
肿瘤坏死因子-Α
Triggering receptor expressed on myeloid cells
Severe acute pancreatitis
Tumor necrosis factoralpha