Abstract-Effects of C-terminal octapeptide of cholecystokinin (CB-CCK) and prostaglandins E1, E2 and F2ai on noradrenaline-induced responses and 3H -noradrenaline release in the gallbladder and sphincter of Oddi of guinea pigs were examined. In the sphincter of Oddi, noradrenaline in low concentrations induced a relaxation which was blocked by either phen tolamine or propranolol, while noradrenaline in high concentrations induced a contraction which was blocked by phentolamine. These results suggest the existence of excitatory and inhibitory a-receptors and inhibitory 8 receptors in the sphincter of Oddi. In the gallbladder, the adrenergic receptors are a-excitatory and (3-inhibitory. CB-CCK (10-9 g/ml) poten tiated both contractile and relaxing responses to noradrenaline, in the gallbladder. The same concentration of prostaglandins potentiated only contractile response to noradrenaline. In the sphincter of Oddi, nor adrenaline-induced responses were not affected by CB-CCK and prosta glandins. Prostaglandins inhibited 3H-efflux evoked by electrical stimu lation, while CB-CCK had no effect on the 3H-efflux from both preparations. These results suggest that CB-CCK enhances the contractile and relaxing responses to noradrenaline, and that prostaglandins act in a similar way on the postsynaptic response and, in addition, inhibit presynaptically the release of noradrenaline in the gallbladder. In the sphincter of Oddi, only prostaglandins inhibit the presynaptic event.