Vertical sleeve gastrectomy is effective in two genetic mouse models of glucagon-like Peptide 1 receptor deficiency

Diabetes. 2013 Jul;62(7):2380-5. doi: 10.2337/db12-1498. Epub 2013 Feb 22.

Abstract

Glucagon-like peptide 1 (GLP-1) is a peptide hormone that is released from the gut in response to nutrient ingestion and that has a range of metabolic effects, including enhancing insulin secretion and decreasing food intake. Postprandial GLP-1 secretion is greatly enhanced in rats and humans after some bariatric procedures, including vertical sleeve gastrectomy (VSG), and has been widely hypothesized to contribute to reduced intake, weight loss, and the improvements in glucose homeostasis after VSG. We tested this hypothesis using two separate models of GLP-1 receptor deficiency. We found that VSG-operated GLP-1 receptor-deficient mice responded similarly to wild-type controls in terms of body weight and body fat loss, improved glucose tolerance, food intake reduction, and altered food selection. These data demonstrate that GLP-1 receptor activity is not necessary for the metabolic improvements induced by VSG surgery.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Body Composition / drug effects
  • Body Composition / physiology*
  • Body Weight / drug effects
  • Body Weight / physiology
  • Eating / drug effects
  • Eating / physiology
  • Exenatide
  • Gastrectomy / methods*
  • Glucagon-Like Peptide 1 / metabolism
  • Glucagon-Like Peptide-1 Receptor
  • Insulin Resistance / physiology
  • Mice
  • Mice, Knockout
  • Obesity / genetics
  • Obesity / metabolism
  • Obesity / surgery*
  • Peptides / pharmacology
  • Postprandial Period
  • Receptors, Glucagon / genetics*
  • Receptors, Glucagon / metabolism
  • Venoms / pharmacology

Substances

  • GLP1R protein, human
  • Glp1r protein, mouse
  • Glp1r protein, rat
  • Glucagon-Like Peptide-1 Receptor
  • Peptides
  • Receptors, Glucagon
  • Venoms
  • Glucagon-Like Peptide 1
  • Exenatide