Gastric loads potentiate inhibition of food intake produced by a cholecystokinin analogue

G. J. Schwartz, L. A. Netterville, P. R. McHugh, T. H. Moran

Research output: Contribution to journalArticlepeer-review

56 Scopus citations


We have proposed that cholecystokinin's (CCK) inhibition of gastric emptying contributes to its ability to inhibit food intake. To directly test this hypothesis in rats, the effect of the presence of a 5-ml gastric saline load on the ability of a long-acting cholecystokinin analogue U-67827E (0.1-10.0 nmol/kg) to inhibit intake of a 0.5 kcal/ml glucose solution was measured. The CCK analogue alone inhibited intake at a threshold dose of 2.5 nmol/kg. Although lower doses of the CCK analogue alone had no effect on subsequent glucose intake, when combined with the gastric load such doses did significantly inhibit intake. Thus the presence of a gastric load reduced the threshold dose of the CCK analogue required to inhibit intake. Furthermore, at suprathreshold doses, the peptide-load combination suppressed intake more than the peptide alone. In addition, administration of 0.5 and 5.0 nmol/kg doses of the CCK analogue inhibited gastric emptying at 10, 20, and 30 min in a dose-dependent fashion. The CCK analogue's inhibition of food intake and gastric emptying were reversed by pretreatment with 100 μg/kg L364,718, indicating that the analogue was having its effects by interacting with specific type A CCK receptors. Together these data support the notion that CCK satiety derives from an integration of the visceral afferent signals generated by CCK's promotion of gastric distension and those produced directly by CCK.

Original languageEnglish (US)
Pages (from-to)R1141-R1146
JournalAmerican Journal of Physiology - Regulatory Integrative and Comparative Physiology
Issue number5 30-5
StatePublished - 1991
Externally publishedYes


  • Feeding
  • Gastric distension
  • Rats
  • Satiety
  • Stomach

ASJC Scopus subject areas

  • Physiology
  • Physiology (medical)


Dive into the research topics of 'Gastric loads potentiate inhibition of food intake produced by a cholecystokinin analogue'. Together they form a unique fingerprint.

Cite this