期刊文献+

TNBS模型大鼠结肠组织中NF-κB、PPAR-γ的表达特点 被引量:3

The Expression Characteristics of NF-κB and PPAR-γ in Colon Tissue of TNBS Rats
下载PDF
导出
摘要 目的观察三硝基苯磺酸(TNBS)造模后第3日、7日、10日、14日大鼠结肠组织中核转录因子-κB(NF-κB)、过氧化物酶体增殖物激活受体-γ(PPAR-γ)表达的变化特点。方法造模组采用TNBS/乙醇溶液灌肠法制作UC大鼠模型,将大鼠分为空白组、造模后3 d组、造模后7 d组、造模后10 d组、造模后14 d组。后4组分别于造模后第3日、7日、10日、14日处死,采用免疫组化法及实时荧光定量PCR法测定各组大鼠结肠组织中NF-κB、PPAR-γ及m RNA表达。结果造模后3 d大鼠结肠NF-κB表达显著上调,10 d、14 d后表达较前逐渐回落;造模后3 d大鼠结肠PPAR-γ表达明显下调,至14 d时其表达逐渐恢复。结论 TNBS大鼠结肠炎是炎症性肠病的良好模型,造模后结肠NF-κB表达上调,PPAR-γ表达受抑制,在造模后14 d后模型自愈较为明显,治疗的疗程选择7~10 d为宜。 Objective:To observe the expression characteristics of NF-κB and PPAR-γ in colon tissue of TNBS rats after successful modeling on 3rdday,7thday,10 thday and 14 thday.Methods:The models were made with TNBS/ethanol solution enema method.The rats were divided into the blank group,3 d group,7 d group,10 d group and 14 d group.The latter four groups were killed according to time.The expression of NF-κB,PPAR-γand m RNA was detected by immunohistochemistry and real-time fluorescence quantitative PCR method.Results:3 days after modeling,NF-κB expression of rat colon was significantly up-regulated,but after 10 days and 14 days,the expression gradually declined.3 days after modeling,PPAR-γ expression of rat colon significantly reduced.Till 14 thday,the expression gradually restored.Conclusion:TNBS colitis in rats is a good model of IBD.After modeling,NF-κB of colon up-regulated and PPAR-γ expression was inhibited.14 d after modeling,self-healing of model is more obvious,and the course of treatment lasting 7 to 10 days is appropriate.
机构地区 江苏省中医院
出处 《中国中医急症》 2016年第8期1461-1464,1487,共5页 Journal of Emergency in Traditional Chinese Medicine
基金 国家自然科学基金委员会青年科学基金项目(81302919) 江苏省中医药局科技项目立项计划(LZ13048) 江苏省中医院高峰学术人才培养工程(k2014yrc13) 江苏省中医院院级课题(Y14076)
  • 相关文献

参考文献15

  • 1XIA J,YUAN J,XIN L,et al.Transcriptome analysis on the inflammatory cell infiltration of nonalcoholic steatohepatitis in bama minipigs induced by a long-term high-fat,high-sucrose diet[J].PLo S One,2014,9(11):1-22.
  • 2Arab HH,AL-Shorbagy MY,Abdallah DM,et al.Telmisartan attenuates colon inflammation,oxidative perturbations and apoptosis in a rat model of experimental inflammatory bowel disease[J].PLo S One,2014,9(5):1-16.
  • 3Morris GP,Beck PL,Herridge MS,et al.Hapten-induced model of chronic inflammation and ulceration in the rat colon[J].Gastroenterology,1989,96(3):795-803.
  • 4盛艳梅,颜晓燕.溃疡性结肠炎动物模型在药效研究中的应用[J].四川生理科学杂志,2006,28(2):65-66. 被引量:5
  • 5郑礼,高振强,王淑仙.大鼠溃疡性结肠炎模型的实验研究[J].中国药理学通报,1998,14(4):370-372. 被引量:99
  • 6Stenson WF.Enhanced synthesis of leukotriene B4 by colonic mucosa ininflammatory bowel disease[J].Gastroenterology,1984,86(3):453-460.
  • 7Krimskym,Yedgars,Aptekarl,et al.Anelioration of TNBs-induced colon inflammation on rats by phospholi-pase A2chhibitor[J].Am J Physiol Gas-trochtest Liver Physiol,2003,285(9):586-592.
  • 8Dargeniog,Farracemg,Cosenzav,et al.Expression of apoptosis-related protein sin rat with induced colitis[J].Int J Colorectal Dis,2004,19(7):451-460.
  • 9朱峰,钱家鸣.实验性炎症性肠病的动物模型[J].胃肠病学,1996,1(2):107-110. 被引量:3
  • 10王皓,欧阳钦,胡仁伟.三硝基苯磺酸结肠炎动物模型的建立[J].胃肠病学,2001,6(1):7-10. 被引量:177

二级参考文献42

共引文献256

同被引文献31

引证文献3

二级引证文献33

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部