Neurotensin and oxyntomodulin-(30-37) potentiate PYY regulation of gastric acid and somatostatin secretions

Am J Physiol. 1993 Jul;265(1 Pt 1):G113-7. doi: 10.1152/ajpgi.1993.265.1.G113.

Abstract

The present study was designed to investigate, in cats provided with both a gastric fistula and a denervated fundic Heidenhain pouch, the effect of peptide YY (PYY) on pentagastrin-stimulated gastric acid and somatostatin secretions and to determine whether neurotensin (NT) and the COOH-terminal octapeptide of oxyntomodulin [Oxm-(30-37)] would modify these secretions. Intravenous infusion of PYY (0.1 nmol.kg-1.h-1), NT (15 nmol.kg-1.h-1), or Oxm-(30-37) (60 nmol.kg-1.h-1) did not affect basal acid secretion. However, they significantly inhibited pentagastrin-stimulated gastric acid output up to 50% (P < 0.01) in the main stomach. Furthermore, they significantly increased gastric somatostatin release by +750, +1,700, and +600% over basal level (P < 0.01) for (in nmol.kg-1.h-1) 0.1 PYY, 15 NT, and 60 Oxm-(30-37), respectively. On the other hand, the effects of 0.1 nmol.kg-1.h-1 PYY were potentiated by subthreshold doses of NT (5 nmol.kg-1.h-1) or Oxm-(30-37) (15 nmol.kg-1.h-1). These findings suggest that there could be a cooperation between the three peptides in the intestinal regulation of gastric secretions.

MeSH terms

  • Animals
  • Cats
  • Drug Synergism
  • Gastric Acid / metabolism*
  • Gastric Mucosa / metabolism
  • Gastrointestinal Hormones / physiology
  • Glucagon-Like Peptides / pharmacology*
  • Neurotensin / pharmacology*
  • Oxyntomodulin
  • Pentagastrin / pharmacology
  • Peptide Fragments / pharmacology*
  • Peptide YY
  • Peptides / physiology*
  • Somatostatin / metabolism*

Substances

  • Gastrointestinal Hormones
  • Oxyntomodulin
  • Peptide Fragments
  • Peptides
  • Peptide YY
  • Neurotensin
  • Somatostatin
  • Glucagon-Like Peptides
  • Pentagastrin