Impaired gastric secretion and lack of trophic responses to hypergastrinemia in M 3 muscarinic receptor knockout mice

Abstract

Background & Aims : The physiologic significance of the M 3 muscarinic receptor is unclear due to an absence of specific ligand. In the present study, M 3 receptor knockout (KO) mice were used to elucidate the role of M 3 receptors in gastric acid secretion and gastric mucosal integrity. Methods : M 3 KO versus wild-type mice aged 1 month to 2 years were included. Gastric acid secretion was assessed by both direct intragastric pH measurement and pylorus ligation. Serum gastrin and gastric mucosal histamine levels were determined by radioimmunoassay and enzyme-linked immunosorbent assay, respectively. Morphologic analysis was performed by both immunohistochemistry and transmission electron microscopy. Results : Fasted M 3 KO mice exhibited higher intragastric pH, lower acid output after pylorus ligation, a lower proportion of active parietal cells, and higher serum gastrin levels than fasted wild-type mice. Acid secretion in response to carbachol, histamine, gastrin 17, and 2-deoxy- d-glucose was impaired in the mutant mice. Although carbachol was still able to cause ∼30% acid output in M 3 KO mice, the acid secretion was inhibited by pirenzepine or famotidine. Despite remarkable hypergastrinemia in M 3 KO mice, there were no trophic responses in the oxyntic mucosa with respect to the mucosal thickness, proliferation rate, and numbers of parietal and enterochromaffin-like cells. Cholecystokinin type 2 receptor antagonist YM022 was without the effect in M 3 KO mice. Conclusions : The present study shows that M 3 receptors are essential for basal acid secretion, a fully acid secretory response to histamine and gastrin, and the trophic responses of oxyntic mucosa to gastrin.