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Effect of Roux-en-Y gastric bypass on the distribution and hormone expression of small-intestinal enteroendocrine cells in obese patients with type 2 diabetes

Authors :
Jens Pedersen
Camilla D. Wahlgren
Ebbe Langholz
Erik Wandall
Viggo B. Kristiansen
Peter Vilmann
Steen Seier Poulsen
Jacob Jelsing
Louise S. Dalbøge
Steffen U. Friis
Filip K. Knop
Brynjulf Mortensen
Jens J. Holst
Sarah Juel Paulsen
Tina Vilsbøll
Nicolai Rhee
Source :
Diabetologia. 58:2254-2258
Publication Year :
2015
Publisher :
Springer Science and Business Media LLC, 2015.

Abstract

We studied the impact of Roux-en-Y gastric bypass (RYGB) on the density and hormonal gene expression of small-intestinal enteroendocrine cells in obese patients with type 2 diabetes.Twelve patients with diabetes and 11 age- and BMI-matched controls underwent RYGB followed by enteroscopy ~10 months later. Mucosal biopsies taken during surgery and enteroscopy were immunohistochemically stained for glucagon-like peptide-1 (GLP-1), peptide YY (PYY), cholecystokinin (CCK), glucose-dependent insulinotropic polypeptide (GIP) and prohormone convertase 2 (PC2) and the expression of GCG (encoding preproglucagon), PYY, CCK, GIP, GHRL (encoding ghrelin), SCT (encoding secretin), NTS (encoding neurotensin) and NR1H4 (encoding farnesoid X receptor) was evaluated.The density of cells immunoreactive for GLP-1, CCK and GIP increased in patients after RYGB and the density of those immunoreactive for GLP-1, PYY, CCK and PC2 increased in controls. In both groups, GHRL, SCT and GIP mRNA was reduced after RYGB while PYY, CCK, NTS and NR1H4 gene expression was unaltered. GCG mRNA was upregulated in both groups.Numerous alterations in the distribution of enteroendocrine cells and their expression of hormonal genes are seen after RYGB and include increased density of GLP-1-, PYY-, CCK-, GIP- and PC2-positive cells, reduced gene expression of GHRL, SCT and GIP and increased expression of GCG.

Details

ISSN :
14320428 and 0012186X
Volume :
58
Database :
OpenAIRE
Journal :
Diabetologia
Accession number :
edsair.doi.dedup.....9d50247c0152f729c44fbc28d6920838
Full Text :
https://doi.org/10.1007/s00125-015-3696-3