Peptide YY, glucagon-like peptide-1, and neurotensin responses to luminal factors in the isolated vascularly perfused rat ileum

Endocrinology. 1998 Sep;139(9):3780-6. doi: 10.1210/endo.139.9.6202.

Abstract

Exposure of the ileum to nutrients markedly inhibits several upper gastrointestinal functions. Hormonal peptides of the ileal wall, i.e. peptide YY (PYY), glucagon-like peptide-1 (GLP-1), and neurotensin (NT), are thought to play a role in this negative feedback mechanism. The present study was conducted to comparatively assess the secretion of PYY, GLP-1, and NT upon luminal infusion of a variety of individual luminal factors in the isolated vascularly perfused rat ileum preparation. PYY, GLP-1, and NT were measured in the portal effluent with specific RIAs. Glucose (250 mM) induced a pronounced release of the three peptides, whereas a physiological concentration of 5 mM did not induce peptide secretion. Peptone (5%, wt/vol) evoked a sustained release of PYY, GLP-1, and NT. Only NT secretion was increased upon luminal administration of 100 mM sodium oleate. Short chain fatty acids (20 mM) evoked an early and transient release of the three peptides. In contrast, taurocholate (20 mM) induced a sustained release of PYY, GLP-1, and NT, but the threshold concentration for peptide release was lower for NT than for PYY or GLP-1. Cellulose or pectin (0.5%, wt/vol) did not modify peptide secretion. In conclusion, glucose and peptone are potent stimulants of PYY, GLP-1, and NT release. Only NT is released upon oleic acid stimulation. Finally, taurocholate is a potent stimulant of the release of the three peptides. Overall, PYY, GLP-1, and NT may participate cooperatively in the ileal brake. As relatively high concentrations of the various stimulants were required to elicit peptide release, it seems likely that this mechanism operates in cases of maldigestion or malabsorption.

MeSH terms

  • Animal Nutritional Physiological Phenomena
  • Animals
  • Fatty Acids / pharmacology*
  • Glucagon / metabolism*
  • Glucagon-Like Peptide 1
  • Ileum / blood supply
  • Ileum / drug effects
  • Ileum / metabolism*
  • In Vitro Techniques
  • Male
  • Neurotensin / metabolism*
  • Peptide Fragments / metabolism*
  • Peptide YY / metabolism*
  • Perfusion
  • Protein Precursors / metabolism*
  • Rats
  • Rats, Wistar
  • Taurocholic Acid / pharmacology*

Substances

  • Fatty Acids
  • Peptide Fragments
  • Protein Precursors
  • Peptide YY
  • Neurotensin
  • Taurocholic Acid
  • Glucagon-Like Peptide 1
  • Glucagon