Tairov M M, Bersimbaev R I, Argutinskaia S V, Salganik R I
Biokhimiia. 1983 Jun;48(6):1035-41.
It was shown that cimetidine, the inhibitor of H2-receptors of histamine, does not affect the activation of adenylate cyclase by prostaglandin E2 (PGE2) in rat gastric mucosa homogenate. At the same time cimetidine completely inhibits the stimulating effect of histamine on the adenylate cyclase activity. Using isolated rat gastric cells separated into fractions rich (to 90%) and poor (up to 25%) of parietal cells, it was demonstrated that the prostaglandin-stimulated adenylate cyclase is localized in the non-parietal (presumably mucoid) cells, while the histamine-sensitive one is localized in parietal acid-producing cells. The mechanisms of histamine and PGE2 action are discussed and a scheme of participation of these substances in regulation of gastric secretion is proposed.
结果表明,组胺H2受体抑制剂西咪替丁不影响前列腺素E2(PGE2)对大鼠胃黏膜匀浆中腺苷酸环化酶的激活作用。同时,西咪替丁完全抑制组胺对腺苷酸环化酶活性的刺激作用。利用分离出的大鼠胃细胞,将其分为富含(达90%)和缺乏(达25%)壁细胞的部分,结果表明,前列腺素刺激的腺苷酸环化酶定位于非壁细胞(可能是黏液细胞),而组胺敏感的腺苷酸环化酶定位于分泌酸的壁细胞。文中讨论了组胺和PGE2的作用机制,并提出了这些物质参与胃分泌调节的示意图。