Cross S A
Histochem J. 1977 Sep;9(5):619-44. doi: 10.1007/BF01002905.
Histamine stimulates acid secretion by the parietal cell and this secretion is inhibited by the histamine H2-receptor antagonists. Whole body autoradiography showed that radioactivity from 14C-histamine was localized in the artery walls of the stomach and in the muscularis mucosae, but that the level in the fundic mucosa was the same as the blood. When the H2-receptor antagonists burimamide, metiamide and cimetidine were labelled with 35S, 14C or 3H and dosed to rats, whole body autoradiography showed that the stomach was predominantly labelled in the glandular mucosa from 5 to 120 min after administration. Microautoradiography in the rat and dog after intravenous injection of [3H]metiamide or [3H]cimetidine demonstrated an uptake of tritium in the parietal cell cytoplasm that was 3- to 4-times greater than that found in adjacent peptic cells or areas of muscularis mucosa. The preferential labelling persisted at a low level up to 6h after injection in the rat. The localization of radioactivity from the H2-antagonists in the parietal cell cytoplasm correlates well with their pharmacological activity in preventing acid secretion from this cell.
组胺刺激壁细胞分泌胃酸,而这种分泌可被组胺H2受体拮抗剂抑制。全身放射自显影显示,14C-组胺的放射性定位于胃的动脉壁和黏膜肌层,但胃底黏膜中的水平与血液中的相同。当用35S、14C或3H标记H2受体拮抗剂布立马胺、甲硫米特和西咪替丁并给大鼠给药时,全身放射自显影显示,给药后5至120分钟,胃主要在腺性黏膜中被标记。给大鼠和狗静脉注射[3H]甲硫米特或[3H]西咪替丁后的显微放射自显影显示,壁细胞胞质中氚的摄取量比相邻的胃蛋白酶细胞或黏膜肌层区域高3至4倍。在大鼠中,注射后长达6小时,这种优先标记一直维持在低水平。H2拮抗剂的放射性在壁细胞胞质中的定位与其阻止该细胞分泌胃酸的药理活性密切相关。