Abstract

Although several studies have revealed the role of different lipid mediators in colitis, the comprehensive analysis of their production across different phases of colitis remained unclear. Here, we performed the following analysis in the dextran sodium sulfate (DSS)-induced colitis model using LC-MS/MS. Oral administration of 2% DSS in mice for 4 days resulted in severe intestinal inflammation by day 7, which gradually subsided by day 18. Based on the disease scoring index (assigned on the basis of fecal condition and weight loss), we defined the phases of colitis as induction (days 0-4), acute inflammation (days 4-7), recovery (days 7-9), and late recovery (days 9-18). Across all phases, 58 lipid mediators were detected in the inflamed colon tissue. In the induction phase, the production of n-6 fatty acid-derived prostaglandin E2 and thromboxane B2 increased by ∼2-fold. In the acute inflammation phase, the production of n-6 fatty acid-derived leukotrienes increased by >10-fold, while that of n-3 fatty acid-derived hydroxyeicosapentaenoic acids and dihydroxyeicosatetraenoic acids decreased. In the recovery phase, a precursor of protectin D1 (17-hydroxydocosahexaenoic acid) increased over 3-fold. These observations suggested dynamic changes in the production of lipid mediators across different phases of the disease and their potential regulation in healing colitis.

Highlights

  • Several studies have revealed the role of different lipid mediators in colitis, the comprehensive analysis of their production across different phases of colitis remained unclear

  • The number of lipid mediators was the lowest on day 7 and the highest on day 9. These results suggested that the major type of fatty acid used for the production of lipid mediators changed from n-6 to n-3 as the disease progressed

  • In the present study, using this disease model, we revealed the dynamic changes taking place in the production of 58 lipid mediators during the progression of colitis

Read more

Summary

Introduction

Several studies have revealed the role of different lipid mediators in colitis, the comprehensive analysis of their production across different phases of colitis remained unclear. A precursor of protectin D1 (17-hydroxydocosahexaenoic acid) increased over 3-fold These observations suggested dynamic changes in the production of lipid mediators across different phases of the disease and their potential regulation in healing colitis.—Hamabata, T., T. Production of lipid mediators across different disease stages of dextran sodium sulfate-induced colitis in mice. In order to investigate the pathophysiology of IBD, chemically induced murine IBD models, such as dextran sodium sulfate (DSS)-induced and trinitrobenzene sulfonic acid (TNBS)-induced colitis models, have been widely employed. DSS exerts direct toxicity toward gut epithelial cells of the basal crypts and affects the integrity of the mucosal barrier This results in acute colitis, which is characterized by bloody diarrhea, colonic ulceration, and granulocyte (neutrophil) infiltration into the colonic mucosa [5]. TNBS haptenizes colonic autologous or microbiota proteins rendering them immunogenic to the host immune system [5]

Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.