Sewing K F, Hannemann H
Pharmacology. 1986;33(5):274-8. doi: 10.1159/000138226.
The inhibitory effects of the histamine H2-receptor antagonists, ranitidine and famotidine on histamine-stimulated gastric acid secretion have been studied in guinea pig isolated, enriched parietal cells using the 14C-aminopyrine accumulation technique. The 14C-aminopyrine accumulation curves in response to histamine were shifted towards the right in a parallel fashion by ranitidine, and in a nonparallel fashion by famotidine. The inhibitory effect of ranitidine, but not that of famotidine, was readily reversed by washing the parietal cells. It is concluded that the histamine H2-receptors in guinea pig parietal cells are blocked competitively and reversibly by ranitidine, but noncompetitively and partially reversibly by famotidine.
利用14C-氨基比林蓄积技术,在豚鼠分离的富壁细胞中研究了组胺H2受体拮抗剂雷尼替丁和法莫替丁对组胺刺激胃酸分泌的抑制作用。雷尼替丁使组胺刺激后的14C-氨基比林蓄积曲线呈平行右移,而法莫替丁则使其呈非平行右移。通过冲洗壁细胞,雷尼替丁的抑制作用可迅速逆转,而法莫替丁的抑制作用则不然。结论是,豚鼠壁细胞中的组胺H2受体被雷尼替丁竞争性和可逆性阻断,但被法莫替丁非竞争性和部分可逆性阻断。