Gastric loads and cholecystokinin synergistically stimulate rat gastric vagal afferents

G. J. Schwartz, P. R. McHugh, T. H. Moran

Research output: Contribution to journalArticlepeer-review

161 Scopus citations


Both gastric preloads and exogenous cholecystokinin (CCK) administration inhibit food intake, and combinations of preloads and CCK suppress feeding to a greater degree than either stimulus delivered alone. A role for the vagus nerve in mediating CCK's inhibition of food intake has been proposed, and gastric vagal afferent fibers respond to both gastric loads and local CCK infusions. To examine whether combined load and CCK stimuli may synergistically augment gastric neural afferent activity at the level of the peripheral vagus, we have examined the gastric vagal afferent responses (n = 8) to a range of gastric saline loads (1, 2, and 3 ml) and exogenous close celiac arterial CCK (10 and 100 pmol) when administered alone or in combination. Gastric loads ineffective in eliciting a significant increase in vagal afferent activity when administered alone became effective when combined with doses of CCK that were subthreshold for the production of a vagal afferent response. Gastric loads that alone were effective in producing a significant vagal afferent response yielded an even greater response when administered in combination with both subthreshold and suprathreshold doses of CCK. These data demonstrate that, in rats, signals produced by combined gastric load and exogenous CCK administration are integrated peripherally and interact synergistically. These results suggest that signals arising from the vagus may provide sufficient information for the synergistic inhibition of food intake produced by combinations of gastric loads and exogenous CCK.

Original languageEnglish (US)
Pages (from-to)R872-R876
JournalAmerican Journal of Physiology - Regulatory Integrative and Comparative Physiology
Issue number4 34-4
StatePublished - 1993
Externally publishedYes


  • feeding inhibition
  • mechanoreceptors

ASJC Scopus subject areas

  • Physiology
  • Physiology (medical)


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