Ondansetron attenuates CCK induced satiety and c-fos labeling in the dorsal medulla

Abstract Serotonin 5-HT 3 antagonists have been suggested for treatment of several disorders involving altered gastrointestinal (GI) function. CCK also has well documented GI actions on both food intake and vago-vagal reflexes. To evaluate potential interactions, the effect of a 5-HT 3 antagonist, ondansetron, on exogenous CCK induced satiety and c-fos activation was determined. Ondansetron reduced both actions of CCK by approximately 50%. The reduction in c-fos was localized to a specific subregion of the dorsal medulla, suggesting that a distinct subpopulation of CCK receptive fibers are modulated by 5-HT 3 ligands. Treatments using 5-HT 3 antagonists also may affect endogenous CCK functions.