Nontargeted Urinary Metabolite Profiling of a Mouse Model of Crohn’s Disease

2009 ◽  
Vol 8 (4) ◽  
pp. 2045-2057 ◽  
Author(s):  
Hui-Ming Lin ◽  
Shelley J. Edmunds ◽  
Nuala A. Helsby ◽  
Lynnette R. Ferguson ◽  
Daryl D. Rowan
2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Elodie Gimier ◽  
Mélissa Chervy ◽  
Allison Agus ◽  
Adeline Sivignon ◽  
Elisabeth Billard ◽  
...  

2016 ◽  
Vol 1 (3) ◽  
pp. eaaf8864-eaaf8864 ◽  
Author(s):  
Bernard C. Lo ◽  
Matthew J. Gold ◽  
Michael R. Hughes ◽  
Frann Antignano ◽  
Yanet Valdez ◽  
...  

2018 ◽  
Vol 119 (8) ◽  
pp. 6743-6755 ◽  
Author(s):  
Suncica Buljevic ◽  
Dijana Detel ◽  
Ester P. Pugel ◽  
Jadranka Varljen

Author(s):  
Hajime Tanaka ◽  
Sivagami Gunasekaran ◽  
Dina Mourad Saleh ◽  
William Theodore Alexander ◽  
David Bedell Alexander ◽  
...  

Both ulcerative colitis and colonic Crohn's disease patients have a significantly increased risk of developing colorectal cancer. bLF is reported to inhibit the development of colon cancer in rats and mice, and in a placebo controlled trial, ingestion of bLF inhibited the growth of intestinal polyps. In addition, in a case study a Crohn's disease patient was reported to have remained in remission for over 7 years while ingesting 1 gram of bLF daily. Thus, bLF has an inhibitory effect on colon carcinogenesis, and it may also promote remission of Crohn's disease. The purpose of the present study was to begin to investigate the effect of bLF on a mouse model of IBD-related colorectal cancer. Azoxymethane (AOM) was used to initiate intestinal cancer and dextran sulfate sodium (DSS) was used to induce IBD-like inflammation in the intestine of C57BL/6 mice. Mice were divided into 4 groups: untreated, bLF alone, AOM+DSS, and AOM+DSS+bLF. At the end of the study, mice given AOM+DSS+LF had a better fecal score, less wounding in the colon, and less weight loss than mice in the AOM+DSS group. However, there were no statistically significant differences between the two groups in tumor burden.


2013 ◽  
Vol 2013 ◽  
pp. 1-8 ◽  
Author(s):  
C. Yuan ◽  
W.-X. Chen ◽  
J.-S. Zhu ◽  
N.-W. Chen ◽  
Y.-M. Lu ◽  
...  

Prohibitin, which can inhibit oxidative stress and mitochondrial dysfunction, has been shown to have significant anti-inflammatory activities. Here, we investigate the effects of altering prohibitin levels in affected tissues in the interleukin-10 knockout (IL-10KO) mouse model with intestinal fibrosis. The aim of this study is to investigate the effects of IL-10 on prohibitin and the role of prohibitin in intestinal fibrosis of murine colitis. After the mice were treated with IL-10, prohibitin expression and localization were evaluated in IL-10KO and wild-type (WT, 129/SvEv) mice. The colon tissue was then investigated and the potential pathogenic molecular mechanisms were further studied. Fluorescence-based quantitative polymerase chain reaction (FQ-PCR) and immunohistochemistry assays revealed a significant upregulation of prohibitin with IL-10 treatment. Furthermore, IL-10 decreases inflammatory cytokines and TGF-β1 in the IL-10KO model of Crohn’s disease and demonstrates a promising trend in decreasing tissue fibrosis. In conclusion, we hypothesize that IL-10 treatment is associated with increased prohibitin and would decrease inflammation and fibrosis in an animal model of Crohn’s disease. Interestingly, prohibitin may be a potential target for intestinal fibrosis associated with inflammatory bowel disease (IBD).


2001 ◽  
Vol 120 (5) ◽  
pp. A36-A36 ◽  
Author(s):  
K KOZAIWA ◽  
K SUGAWARA ◽  
C MOSKALUK ◽  
S MATSUMOTO ◽  
F COMINELLI

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