4.5 Article

A Quantitative Analysis of Colonic Mucosal Oxylipins and Endocannabinoids in Treatment-Naive and Deep Remission Ulcerative Colitis Patients and the Potential Link With Cytokine Gene Expression

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INFLAMMATORY BOWEL DISEASES
卷 25, 期 3, 页码 490-497

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OXFORD UNIV PRESS INC
DOI: 10.1093/ibd/izy349

关键词

EPEA; DHEA; IBD; PUFA; eicosanoids

资金

  1. University of Tromso-The Arctic University of Norway
  2. Helse Nord RHF [SFP-1134-13]

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Background The bioactive metabolites of omega 3 and omega 6 polyunsaturated fatty acids (-3 and -6) are known as oxylipins and endocannabinoids (eCBs). These lipid metabolites are involved in prompting and resolving the inflammatory response that leads to the onset of inflammatory bowel disease (IBD). This study aims to quantify these bioactive lipids in the colonic mucosa and to evaluate the potential link to cytokine gene expression during inflammatory events in ulcerative colitis (UC). Methods Colon biopsies were taken from 15 treatment-naive UC patients, 5 deep remission UC patients, and 10 healthy controls. Thirty-five oxylipins and 11 eCBs were quantified by means of ultra-high-performance liquid chromatography coupled with tandem mass spectrometry. Levels of mRNA for 10 cytokines were measured by reverse transcription polymerase chain reaction. Results Levels of -6-related oxylipins were significantly elevated in treatment-naive patients with respect to controls, whereas the levels of -3 eCBs were lower. 15S-Hydroxy-eicosatrienoic acid (15S-HETrE) was significantly upregulated in UC deep remission patients compared with controls. All investigated cytokines had significantly higher mRNA levels in the inflamed mucosa of treatment-naive UC patients. Cytokine gene expression was positively correlated with several -6 arachidonic acid-related oxylipins, whereas negative correlation was found with lipoxin, prostacyclin, and the eCBs. Conclusions Increased levels of -6-related oxylipins and decreased levels of -3-related eCBs are associated with the debut of UC. This highlights the altered balance between pro- and anti-inflammatory lipid mediators in IBD and suggests potential targets for intervention.

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