Important Role of the GLP-1 Axis for Glucose Homeostasis after Bariatric Surgery

Pierre Larraufie(Wellcome/MRC Institute of Metabolic Science), Geoffrey Roberts(Wellcome/MRC Institute of Metabolic Science), Anne K. McGavigan(Wellcome/MRC Institute of Metabolic Science), Richard G. Kay(Wellcome/MRC Institute of Metabolic Science), Joyce Li(University of Massachusetts Chan Medical School), Andrew B. Leiter(University of Massachusetts Chan Medical School), Audrey Melvin(Wellcome/MRC Institute of Metabolic Science), Emma K. Biggs(Wellcome/MRC Institute of Metabolic Science), Peter Ravn, Kathleen Davy, David C. Hornigold, Giles S.H. Yeo(Wellcome/MRC Institute of Metabolic Science), Richard Hardwick(Addenbrooke's Hospital), Frank Reimann(Wellcome/MRC Institute of Metabolic Science), Fiona M. Gribble(Wellcome/MRC Institute of Metabolic Science)
Cell Reports
February 1, 2019
Cited by 165Open Access
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Abstract

Bariatric surgery is widely used to treat obesity and improves type 2 diabetes beyond expectations from the degree of weight loss. Elevated post-prandial concentrations of glucagon-like peptide 1 (GLP-1), peptide YY (PYY), and insulin are widely reported, but the importance of GLP-1 in post-bariatric physiology remains debated. Here, we show that GLP-1 is a major driver of insulin secretion after bariatric surgery, as demonstrated by blocking GLP-1 receptors (GLP1Rs) post-gastrectomy in lean humans using Exendin-9 or in mice using an anti-GLP1R antibody. Transcriptomics and peptidomics analyses revealed that human and mouse enteroendocrine cells were unaltered post-surgery; instead, we found that elevated plasma GLP-1 and PYY correlated with increased nutrient delivery to the distal gut in mice. We conclude that increased GLP-1 secretion after bariatric surgery arises from rapid nutrient delivery to the distal gut and is a key driver of enhanced insulin secretion.


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