Effect of Truncated Glucagon-Like peptide-1 [proglucagon-(78-107) Amide] on Endocrine Secretion From Pig Pancreas, Antrum, and Nonantral Stomach

Endocrinology. 1988 Oct;123(4):2009-13. doi: 10.1210/endo-123-4-2009.

Abstract

We studied the effect of truncated glucagon-like peptide-1 [naturally occurring GLP-1; proglucagon-(78-107) amide], a potent insulinotropic peptide from the pig ileum, on endocrine and exocrine secretion of potential gastrointestinal target organs using isolated perfused preparations of the porcine pancreas, antrum, and nonantral part of the stomach. Truncated GLP-1 significantly increased somatostatin secretion from the pancreas at 10(-10) mol/liter and more than doubled the secretion at 10(-9) mol/liter, but had no effect on either somatostatin or gastrin secretion from the antrum or on somatostatin secretion from the nonantral stomach in concentrations up to 10(-8) mol/liter. Insulin secretion from the pancreas (with 7 mmol/liter glucose in the perfusate) increased 2-fold with truncated GLP-1 at 10(-10) mol/liter and almost 5-fold at 10(-9) mol/liter. Pancreatic glucagon secretion was inhibited by 50% at 10(-10) mol/liter and by 70-80% at 10(-9) mol/liter. Full-length GLP-1 [proglucagon-(72-107)] and GLP-2 [proglucagon-(126-159)] had no effect on hormone secretion from any of the perfused organs. It is concluded that truncated GLP-1 may participate in an entero-insular control of pancreatic endocrine secretion.

MeSH terms

  • Animals
  • Gastric Mucosa / metabolism*
  • Glucagon / metabolism
  • Glucagon / physiology*
  • Glucagon-Like Peptide 1
  • Ileum / physiology
  • In Vitro Techniques
  • Insulin / metabolism
  • Insulin Secretion
  • Islets of Langerhans / metabolism*
  • Organ Specificity
  • Peptide Fragments / physiology*
  • Protein Precursors / physiology*
  • Pyloric Antrum
  • Somatostatin / metabolism
  • Swine

Substances

  • Insulin
  • Peptide Fragments
  • Protein Precursors
  • Somatostatin
  • Glucagon-Like Peptide 1
  • Glucagon