GLP-1 enhances β-cell response to protein ingestion and bariatric surgery amplifies it

Obesity (Silver Spring). 2025 Jan;33(1):104-115. doi: 10.1002/oby.24182. Epub 2024 Dec 5.

Abstract

Objective: The glycemic-independent actions of glucagon-like peptide-1 (GLP-1) in the prandial state in humans are unknown. We examined the contribution of GLP-1 to β-cell secretory response (primary endpoint) and glucose metabolism during protein ingestion under basal glycemia, as well as whether these responses are affected by rerouted gut after gastric bypass (GB) or sleeve gastrectomy (SG).

Methods: Insulin secretion rate (ISR) and glucose fluxes during a 50-g oral protein load were compared among 10 nondiabetic individuals with GB, 9 with SG, and 7 non-operated controls (CN), with and without intravenous infusion of exendin(9-39) (Ex-9), a GLP-1 receptor (GLP-1R) antagonist.

Results: Blocking GLP-1R increased glucose before and after protein ingestion and decreased β-cell sensitivity to glucose in the first 30 min of protein ingestion in all three groups (p < 0.05). Reduction in the premeal ISR by Ex-9 infusion was only observed in CN, whereas diminished prandial ISR3h by GLP-1R blockade was only observed in GB and SG (p < 0.05 for interaction). GLP-1R blockade enhanced post-protein insulin action in GB and SG, but not in CN, and exaggerated endogenous glucose production only GB (p < 0.05 for interaction).

Conclusions: These findings are consistent with both pancreatic and extra-pancreatic roles for GLP-1 during protein ingestion in humans that are exaggerated by bariatric surgery.

MeSH terms

  • Adult
  • Bariatric Surgery
  • Blood Glucose* / metabolism
  • Dietary Proteins / administration & dosage
  • Dietary Proteins / pharmacology
  • Female
  • Gastrectomy / methods
  • Gastric Bypass*
  • Glucagon-Like Peptide 1* / metabolism
  • Glucagon-Like Peptide-1 Receptor* / agonists
  • Glucagon-Like Peptide-1 Receptor* / metabolism
  • Humans
  • Insulin Secretion* / drug effects
  • Insulin* / blood
  • Insulin* / metabolism
  • Insulin-Secreting Cells* / drug effects
  • Insulin-Secreting Cells* / metabolism
  • Male
  • Middle Aged
  • Peptide Fragments / pharmacology
  • Receptors, Glucagon / metabolism

Substances

  • Glucagon-Like Peptide 1
  • Insulin
  • Blood Glucose
  • exendin (9-39)
  • Glucagon-Like Peptide-1 Receptor
  • Dietary Proteins
  • Peptide Fragments
  • GLP1R protein, human
  • Receptors, Glucagon