Prostaglandin E receptor subtypes involved in stimulation of gastroduodenal bicarbonate secretion in rats and mice

• Published in: Journal of physiology and pharmacology : an official journal of the Polish Physiological Society Vol. 50; no. 2; pp. 155 - 167
• Main Authors: Takeuchi, K, Ukawa, H, Furukawa, O, Kawauchi, S, Araki, H, Sugimoto, Y, Ishikawa, A, Ushikubi, F, Narumiya, S
• Format: Journal Article
• Language: English
• Published: Poland 01.06.1999
• Subjects: Animals; Anti-Ulcer Agents - pharmacology; Bicarbonates - metabolism; Dinoprostone - pharmacology; Duodenum - drug effects; Duodenum - secretion; Gastric Mucosa - drug effects; Gastric Mucosa - secretion; Intestinal Mucosa - drug effects; Intestinal Mucosa - metabolism; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Rats; Rats, Sprague-Dawley; Receptors, Prostaglandin E - drug effects; Receptors, Prostaglandin E - physiology; Receptors, Prostaglandin E, EP3 Subtype
• ISSN: 0867-5910

We investigated prostaglandin E (EP) receptor subtypes responsible for the HCO3- stimulatory action of prostaglandin E2 (PGE2) in the gastroduodental mucosa, by examining the effects of various prostanoids with subtype specific EP receptor agonists in rats and those of PGE2 in knockout mice lacking EP1 or EP3 receptors. In rats, gastric HCO3- secretion was stimulated by i.v. administration of PGE2, 17-phenyl PGE2 the selective EP1 agonist as well as sulprostone the EP1 and EP3 agonist, but was not affected by other EP agonists such as butaprost the selective EP2 agonist, ONO-NT-012 the selective EP3 agonist or 11-deoxy PGE1 the EP3 and EP4 agonist. In contrast, the HCO3- secretion in rat duodenums was stimulated by PGE2, sulprostone, ONO-NT-012 as well as 11-deoxy PGE1 but not affected by either 17-phenyl PGE2 or butaprost. The HCO stimulatory effect of sulprostone in the stomach was significantly inhibited by ONO-AE-829, the selective EP1 antagonist. On the other hand, PGE2 applied topically to the mucosa for 10 min caused a dose-dependent increase of HCO3- secretion in both the stomach and duodenum of wild-type mice. The HCO3- stimulatory action of PGE2 in the stomach was also observed dose-dependently in knockout mice lacking EP3-receptors but was absent in EP1-receptor knockout mice, while the stimulatory effect in the duodenum was observed in EP1-receptor knockout mice, similar to wild-type animals, but not in knockout mice lacking EP3-receptors. These results indicate that PGE2 stimulates HCO3- secretion via different EP receptor subtypes in the stomach and duodenum; the former is mediated by EP1-receptors, while the latter mediated by EP3-receptors.