Skip to main content
Log in

Impact of probiotics on toll-like receptor 4 expression in an experimental model of ulcerative colitis

  • Published:
Journal of Huazhong University of Science and Technology [Medical Sciences] Aims and scope Submit manuscript

Summary

Toll-like receptors (TLRs) are key components of the innate immune system which trigger antimicrobial host defense responses. This study aimed to investigate the impact of probiotics (Lactobacillus, Bifiidobacterium) on the expression of TLR4 and tumor necrosis factor-alpha (TNF-α) in the colon mucosa of rat experimental ulcerative colitis model induced by trinitrobenzene sulfonic acid (TNBS)/ethanol and immune complexes. The gross and histological changes of the colonic mucosa were observed and assessed by the means-standard deviation and independent samples t-test. The protein expression levels of TLR4 and TNF-α were detected by using immunohistochemistry and Western blotting, respectively. It was revealed that there was visible infiltration of inflammatory cells, formation of crypt abscess, and the reduction of goblet cells in the colon tissue of experimental models. As compared with the control group, the levels of TLR4 and TNF-α protein were significantly increased in the model group (P<0.01 for both). No significant difference was found in the expression of TLR4 and TNF-α between the two-week probiotics treatment group and the model group (P>0.05), whereas significant reductions were shown in rats which were treated with probiotics for four weeks as compared with the model group (P<0.01). There was no significant difference between two probiotics-treated groups. Our results implied that probiotics were likely to play a key role in protecting ulcerative colitis by reducing the inflammatory factor TNF-α expression through inhibiting the TLR4 expression in the colon tissue of experimental models.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Sartor RB. Microbial influences in inflammatory bowel diseases. Gastroenterology 2008,134(2):577–594

    Article  PubMed  CAS  Google Scholar 

  2. Xavier RJ, Podolsky DK. Unravel1ing the pathogenesis of inflammatory bowel disease. Nature, 2007,448(7152): 427–434

    Article  PubMed  CAS  Google Scholar 

  3. Xu SY, Bian RL, Chen X. Experimental methodology of pharmacology. Beijing: People’s Medical Publishing House, 1991:11

    Google Scholar 

  4. Cooper HS, Murthy SN, Shah RS, et al. Clinic pathologic study of dextran sulfate sodium experim ental murine colitis. Lab Invest, 1993,69(2):238–249

    PubMed  CAS  Google Scholar 

  5. Kaser A, Zeissig S, Blumberg RS. Inflammatory bowel disease. Annu Rev Immunol, 2010,28(2):562–573

    Google Scholar 

  6. Sartor RB. Mechanisms of disease: pathogenesis of crohn’s disease and ulcerative colitis. Nat Clin Pract Gatroenterol Hepatol, 2006,3(7):390–406

    Article  CAS  Google Scholar 

  7. Blam ME, Stein RB, Lichtenstein GR. Integrating antitumor necrosis factor therapy in inflammatory bowel disease: current and future perspectives. Am J Gastroenterol, 2001,96(7):1977–1997

    PubMed  CAS  Google Scholar 

  8. Kato K, Mizuno S, Umesaki Y, et al. Randomized placebo-controlled trial assessing the effect of bifidobacteria.-fermented milk on active ulcerative colitis. Aliment Pharmacol Ther, 2004,20(10):1133–1141

    Article  PubMed  CAS  Google Scholar 

  9. Rioux K, Fedorak R. Probiotics in the treatment of inflammatory bowel disease. J Clin Gastroenterol, 2006,40(3):260–263

    Article  PubMed  Google Scholar 

  10. Kuhbacher T, Ott SJ, Helwig U, et al. Bacterial and fungal microbiota in relation to probiotic therapy (VSL#3) in pouchitis. Gut, 2006,55(6):833–841

    Article  PubMed  CAS  Google Scholar 

  11. Rachmilewitz D, Karmeli F, Shteingart S, et al. Immunostimulatory oligonuc1eotides inhibit colonic proinflammatory cytokine production in ulcerative colitis. Inflamm Bowel Dis, 2006,12(5):339–345

    Article  PubMed  Google Scholar 

  12. Siddique I, Khan I. Mechanism of regulation of Na-H exchanger in inflammatory bowel disease: Role of TLR4 signaling mechanism. Dig Dis Sci, 2011,56(6):1656–1662

    Article  PubMed  CAS  Google Scholar 

  13. Rutella S, Locatelli F. Intestinal dendritic cells in the pathogenesis of inflammatory bowel disease. World J Gastroenterol, 2011,17(33):3761–3775

    Article  PubMed  CAS  Google Scholar 

  14. Manolakis AC, Kapsoritakis AN, Kapsoritaki A, et al. Readressing the role of Toll-like receptor-4 alleles in inflammatory bowel disease: colitis, smoking, and seroreactivity. Dig Dis Sci, 2013,58(2):371–380

    PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding authors

Correspondence to Jun Liu  (刘 俊) or Hong-yu Ren  (任宏宇).

Additional information

The authors contributed equally to this work.

This project was supported the grants from the Natural Science Foundation of Hubei province (No. 2012FFB02325) and the National Natural Science Foundation of China (No. 81000159).

Rights and permissions

Reprints and permissions

About this article

Cite this article

Yang, X., Fu, Y., Liu, J. et al. Impact of probiotics on toll-like receptor 4 expression in an experimental model of ulcerative colitis. J. Huazhong Univ. Sci. Technol. [Med. Sci.] 33, 661–665 (2013). https://doi.org/10.1007/s11596-013-1177-9

Download citation

  • Received:

  • Revised:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11596-013-1177-9

Key words

Navigation