Inhibition of indoleamine 2,3-dioxygenase augments inflammation in the trinitrobenzene sulfonic acid (TNBS) colitis model in mice

2003 ◽  
Vol 124 (4) ◽  
pp. A486
Author(s):  
Gregory J. Gurtner ◽  
Rodney Newberry ◽  
Suzanne Shloemann ◽  
Keely McDonald ◽  
William F. Stenson
2003 ◽  
Vol 125 (6) ◽  
pp. 1762-1773 ◽  
Author(s):  
Gregory J Gurtner ◽  
Rodney D Newberry ◽  
Suzanne R Schloemann ◽  
Keely G McDonald ◽  
William F Stenson

1999 ◽  
Vol 189 (8) ◽  
pp. 1169-1180 ◽  
Author(s):  
Taeko Dohi ◽  
Kohtaro Fujihashi ◽  
Paul D. Rennert ◽  
Koichi Iwatani ◽  
Hiroshi Kiyono ◽  
...  

To investigate the potential involvement of T helper (Th)2-type responses in murine models of intestinal inflammation, we used trinitrobenzene sulfonic acid (TNBS)–hapten to induce inflammatory bowel disease in situations where Th1-type responses with interferon (IFN)-γ synthesis are either diminished or do not occur. Intracolonic administration of TNBS to either normal (IFN-γ+/+) or Th1-deficient IFN-γ knockout (IFN-γ−/−) BALB/c mice resulted in significant colitis. In IFN-γ−/− mice, crypt inflammation was more severe than in IFN-γ+/+ mice and was accompanied by hypertrophy of colonic patches with a lymphoepithelium containing M cells and distinct B and T cell zones resembling Peyer's patches. Hapten-specific, colonic patch T cells from both mouse groups exhibited a Th2 phenotype with interleukin (IL)-4 and IL-5 production. TNBS colitis in normal mice treated with anti–IL-4 antibodies or in IL-4−/− mice was less severe than in either IFN-γ+/+ or IFN-γ−/− mice. Our findings now show that the Th2-type responses in TNBS colitis are associated with colonic patch enlargement and inflammation of the mucosal layer and may represent a model for ulcerative colitis.


2020 ◽  
Vol 158 (6) ◽  
pp. S-1019-S-1020
Author(s):  
Artin Soroosh ◽  
Carl R. Rankin ◽  
Kai Fang ◽  
Zulfiqar A. Lokhandwala ◽  
Ivy Ka Man Law ◽  
...  

2008 ◽  
Vol 233 (10) ◽  
pp. 1301-1308 ◽  
Author(s):  
Hanumantha R. Ancha ◽  
Ravi R. Kurella ◽  
Christine C. McKimmey ◽  
Stanley Lightfoot ◽  
Richard F. HartY

Previous experiments in rats with chemically induced colitis have shown that the antioxidant N-acetylcysteine plus mesalamine (5-ASA) exerted a significantly greater therapeutic effect in promoting mucosal healing when compared to either agent alone. The aims of the present study were to compare the effects of three antioxidants plus mesalamine vs. 5-ASA alone in treatment of colitis induced by trinitrobenzene sulfonic acid (TNBS) in rats. Methods: Three days following induction of TNBS colitis, rats received 8 days of rectal therapy with 5-ASA, or 5-ASA plus vitamin C (ascorbic acid), 5-ASA plus phenyl butylnitrone (PBN) and 5-ASA plus vitamin E (α-tocopherol). Distal colonic tissues were examined for microscopic colitis and myeloperoxidase (MPO) activity. Results: Global assessments of microscopic colitis induced by TNBS indicated that 5-ASA alone significantly changed colonic injury by −31%. Combination therapy with ascorbic acid plus 5-ASA or α-tocopherol plus 5-ASA caused further significant change in TNBS colitis by −65 and −82%, respectively. Each of these values was significantly below scores observed with 5-ASA as monotherapy. Reduction in colitis with PBN plus 5-ASA was not different from 5-ASA alone. MPO activity was decreased significantly in response to monotherapy with 5-ASA and each of the antioxidants plus 5-ASA when compared to TNBS. α-Tocopherol plus 5-ASA, however, was the only treatment strategy that reduced significantly MPO activity below that recorded for 5-ASA alone. In conclusion, our results indicate that antioxidants other than N-acetylcysteine significantly enhance the therapeutic effectiveness of 5-ASA in the treatment of TNBS colitis. α-Tocopherol plus 5-ASA exerted profound anti-inflammatory and reparative effects upon colitis induced by TNBS.


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