期刊文献+

双歧杆菌对溃疡性结肠炎大鼠肠黏膜上皮细胞Toll样受体2、4及NF-κB基因表达的影响 被引量:6

Effect of Bifidobacterium on expressions of TLR2,TLR4 and NF-κB genes in the intestinal mucosa of rats with ulcerative colitis
原文传递
导出
摘要 目的观察双歧杆菌(Bf)活制剂对大鼠溃疡性结肠炎(UC)肠黏膜上皮细胞(IECs)TLR2、TLR4、NF-κB基因表达的影响。方法 60只SPF级SD大鼠随机分3组:空白对照组、模型组、Bf组。模型组和Bf组大鼠建立TNBS诱导的UC模型。造模成功后,Bf组予双歧杆菌活菌制剂灌服,空白对照组及模型组不予任何处理。3周后处死全部大鼠,观察一般情况的变化,分离、提取IECs中的总RNA,RT-PCR法检测TLR2、TLR4的表达,免疫组化法检测TLR4、NF-κB表达。结果①Bf组症状、组织损害均较模型组明显减轻。②模型组TLR2、TLR4、NF-κB表达显著高于Bf组与空白对照组(P<0.01)。结论 UC组大鼠结肠上皮细胞TLR2、TLR4及NF-κB基因高表达,Bf组表达明显降低,推测Bf可通过抑制大鼠肠黏膜细胞TLR2、TLR4、NF-κB的表达而缓解肠道的炎症反应。 Objective To investigate the effect of Bifidobacterium(Bf)on expressions of toll-like receptor 2(TLR2),TLR4 and nuclear factor κB(NF-κB) genes in the intestinal mucosa of rats with ulcerative colitis(UC).Methods The rats were randomly divided into three groups: the blank control group,the model control group and the Bf group.UC was induced by 2,4,6-trinitrobenzene sulphonic acid(2,4,6-TNBS)and 100% alcohol(1∶ 1,V/V)in the model group and the Bf group.The rats in the Bf group were given Bf by oral gavage after the model was set up.Three weeks later,the rats were killed and total RNA from intestinal epithelial cells(IECs) was extracted for the detection of TLR2,TLR4 and NF-κB.Results ①Both symptoms and lesions of colonic mucosa in the Bf group were slighter than those in the model group.②Expressions of TLR2,TLR4 and NF-κB in the model group were significantly higher than that in the Bf group and blank control group(P〈0.01).Conclusion High expressions of TLR2,TLR4 and NF-κB genes can be seen in colonic mucosa of rats with UC.Bf can relieve inflammation in the intestinal mucous membrane by inhibiting expressions of TLR2,TLR4 and NF-κB.
出处 《山东大学学报(医学版)》 CAS 北大核心 2011年第5期10-14,共5页 Journal of Shandong University:Health Sciences
基金 山东省自然科学基金资助项目(ZR2009CL006)
关键词 溃疡性结肠炎 双歧杆菌 TOLL样受体2 TOLL样受体4 核因子-KB Ulcerative colitis; Bifidobacterium; Toll-like receptor 2; Toll-like receptor 4; Nuclear factor κB;
  • 相关文献

参考文献3

二级参考文献55

  • 1Benoit Foligne,Sophie Nutten,Corinne Grangette,Véronique Dennin,Denise Goudercourt,Sabine Poiret,Joelle Dewulf,Dominique Brassart,Annick Mercenier,Bruno Pot.Correlation between in vitro and in vivo immunomodulatory properties of lactic acid bacteria[J].World Journal of Gastroenterology,2007,13(2):236-243. 被引量:22
  • 2Buhner S,Buning C,Genschel J,Kling K,Herrmann D,Dignass A,Kuechler I,Krueger S,Schmidt HH,Lochs H.Genetic basis for increased intestinal permeability in families with Crohn's disease:role of CARD15 3020insC mutation? Gut 2006; 55:342-347.
  • 3Gassier N,Rohr C,Schneider A,Kartenbeck J,Bach A,Obermuller N,Otto HF,Autschbach F.Inflammatory bowel disease is associated with changes of enterocytic junctions.Am J Physiol Gastrointest Liver Physiol 2001; 281:G216-G228.
  • 4Xavier RJ,Podolsky DK.Unravelling the pathogenesis of inflammatory bowel disease.Nature 2007; 448:427-434.
  • 5Kabashima K,Saji T,Murata T,Nagamachi M,Matsuoka T,Segi E,Tsuboi K,Sugimoto Y,Kobayashi T,Miyachi Y,Ichikawa A,Narumiya S.The prostaglandin receptor EP4 suppresses colitis,mucosal damage and CD4 cell activation in the gut.J Clin Invest 2002; 109:883-893.
  • 6Atreya I,Atreya R,Neurath MF.NF-kappaB in inflammatory bowel disease.J Intern Med 2008; 263:591-596.
  • 7Neish AS,Gewirtz AT,Zeng H,Young AN,Hobert ME,Karmali V,Rao AS,Madara JL.Prokaryotic regulation of epithelial responses by inhibition of IkappaB-alpha ubiquitination.Science 2000; 289:1560-1563.
  • 8Lee J,Gonzales-Navajas JM,Raz E.The "polarizingtolerizing" mechanism of intestinal epithelium:its relevance to colonic homeostasis.Semin Immunopathol 2008; 30:3-9.
  • 9Cario E,Gerken G,Podolsky DK.Toll-like receptor 2 enhances ZO-1-associated intestinal epithelial barrier integrity via protein kinase C.Gastroenterology 2004; 127:224-238.
  • 10Cooney R,Jewell D.The genetic basis of inflammatory bowel disease.Dig Dis 2009; 27:428-442.

共引文献74

同被引文献24

  • 1Sang, Li-Xuan,Chang, Bing,Zhang, Wen-Liang,Wu, Xiao-Mei,Li, Xiao-Hang,Jiang, Min.Remission induction and maintenance effect of probiotics on ulcerative colitis: A meta-analysis[J].World Journal of Gastroenterology,2010,16(15):1908-1915. 被引量:44
  • 2王长文,张岚,马洪波.双歧杆菌对肠黏膜粘附及免疫调节功能的研究进展[J].吉林医药学院学报,2010,31(1):42-45. 被引量:18
  • 3杨沽彬,郭兴华.乳酸菌生物学基础及应用[M].北京:中国轻工业出版社,1996.
  • 4Marteau P, Rdevrese M,Cellier CJ,et al. Protection from gastrointestinal disease with the use of probiotics [J]. Am J Clin Nutr,2001,73(2) :430-436.
  • 5Siqqers RH, Hzckam DJ. The role of innate immune-stimulated ep- ithelial apoptosis during gastrointestinal inflammatory diseases[J]. Cell Mol Life Sci,2011,68(22):3623-3634.
  • 6Siddique I,Khan I. Mechanism of regulation of Na-H exchanger in inflammatory bowel disease: role of TLR-4 signaling mechanism [J]. Diq Dis Sci,2011,56(6) : 1656-1662.
  • 7Chow DK, Leong RW, Tsoi KK, et al. Long-term follow-up of ulcerative colitis in the Chinese population[J]. Am J Gastroenterol, 2009,104 (3) t 647-654.
  • 8WU T F, CAR ATI C J, MAENAUGHTON W K,etal. Contractile activity of lymphatic vessels is altered inthe TNBS model of guinea pig ileitis[J]. Am J Physiol-Gastmintest Liver Physiol,2006 ,291:566 - 574.
  • 9PURRIE E,MACFARLANE S,THOMSON G,et al.Toll-like receptors-2 ,-3 and-4 expression patterns onhuman colon and their regulation by mucosal-associatedbacteria[J]. Immunology,2005,115:565 -574.
  • 10TOSHCHAKOV V Y’SZMACINSKI H,COUTUREL A,et al. Targeting TLR4 signaling by TLR4 Toll/IL-1 receptordomain-derived decoy peptides : identifica-tion of the TLR4 Toll/IL-1 receptor domain dimeriza-tion interface[J]. J Immunol,2011,186 :4819 - 4827.

引证文献6

二级引证文献80

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