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Melanocortin 3,5 receptors immunohistochemical expression in colonic mucosa of inflammatory bowel disease patients: A matter of disease activity?
Melanocortin 3 and 5 receptors ( MC R and MC R) belong to the melanocortin family. However, data regarding their role in inflammatory bowel diseases (IBD) are currently unavailable. This study aims to ascertain their expression profiles in the colonic mucosa of Crohn's disease (CD) and ulcerati...
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Published in: | World journal of gastroenterology : WJG 2024-03, Vol.30 (9), p.1132-1142 |
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Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | Melanocortin 3 and 5 receptors (
MC
R and MC
R) belong to the melanocortin family. However, data regarding their role in inflammatory bowel diseases (IBD) are currently unavailable.
This study aims to ascertain their expression profiles in the colonic mucosa of Crohn's disease (CD) and ulcerative colitis (UC), aligning them with IBD disease endoscopic and histologic activity.
Colonic mucosal biopsies from CD/UC patients were sampled, and immunohistochemical analyses were conducted to evaluate the expression of MC
R and MC
R. Colonic sampling was performed on both traits with endoscopic scores (Mayo endoscopic score and CD endoscopic index of severity) consistent with inflamed mucosa and not consistent with disease activity (
normal appearing mucosa).
In both CD and UC inflamed mucosa, MC
R (CD: + 7.7 fold
normal mucosa,
< 0.01; UC: + 12 fold
normal mucosa,
< 0.01) and MC
R (CD: + 5.5 fold
normal mucosa,
< 0.01; UC: + 8.1 fold
normal mucosa,
< 0.01) were significantly more expressed compared to normal mucosa.
MC
R and MC
R are expressed in the colon of IBD patients. Furthermore, expression may differ according to disease endoscopic activity, with a higher degree of expression in the traits affected by disease activity in both CD and UC, suggesting a potential use of these receptors in IBD pharmacology. |
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ISSN: | 1007-9327 2219-2840 |
DOI: | 10.3748/wjg.v30.i9.1132 |