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Important Role of the GLP-1 Axis for Glucose Homeostasis after Bariatric Surgery.
- Source :
-
Cell reports [Cell Rep] 2019 Feb 05; Vol. 26 (6), pp. 1399-1408.e6. - Publication Year :
- 2019
-
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.<br /> (Copyright © 2019 The Authors. Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Adult
Animals
Enteroendocrine Cells metabolism
Female
Glucagon-Like Peptide 1 blood
Humans
Hypoglycemic Agents adverse effects
Hypoglycemic Agents therapeutic use
Insulin Secretion
Intestinal Mucosa metabolism
Male
Mice
Mice, Inbred C57BL
Middle Aged
Obesity drug therapy
Obesity surgery
Peptide Fragments adverse effects
Peptide Fragments therapeutic use
Peptide YY metabolism
Postoperative Period
Transcriptome
Bariatric Surgery
Glucagon-Like Peptide 1 metabolism
Glucose metabolism
Homeostasis
Obesity metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2211-1247
- Volume :
- 26
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Cell reports
- Publication Type :
- Academic Journal
- Accession number :
- 30726726
- Full Text :
- https://doi.org/10.1016/j.celrep.2019.01.047