Cheret A M, Scarpignato C, Lewin M J, Bertaccini G
Pharmacology. 1984;28(5):268-74. doi: 10.1159/000137973.
The effect of cimetidine and two new histamine H2-receptor antagonists, oxmetidine and SKF 93479, on histamine-stimulated adenylate cyclase activity was studied in guinea pig gastric mucosal cells. Histamine stimulated the enzyme activity in concentration-dependent fashion. The concentration-response curve of histamine was progressively shifted to the right in the presence of increasing concentrations of each antagonist. The Schild plot gave a straight line for all three compounds, with a slope not significantly different from unity and this suggested a competitive antagonism. The calculated pA2 values were 8.45 +/- 0.20, 7.73 +/- 0.21 and 6.81 +/- 0.15 for SKF 93479, oxmetidine and cimetidine, respectively. These results are in accordance with the pharmacological potencies of the antagonists reported on isolated heart preparation and on gastric secretion in vivo. Therefore, the inhibition of histamine-sensitive adenylate cyclase of gastric cells may represent an additional tool for the in vitro evaluation of the H2-receptor antagonists.
在豚鼠胃黏膜细胞中研究了西咪替丁以及两种新型组胺H2受体拮抗剂奥美替丁和SKF 93479对组胺刺激的腺苷酸环化酶活性的影响。组胺以浓度依赖的方式刺激该酶活性。在每种拮抗剂浓度增加的情况下,组胺的浓度-反应曲线逐渐向右移动。Schild图对所有三种化合物均给出一条直线,斜率与1无显著差异,这表明存在竞争性拮抗作用。SKF 93479、奥美替丁和西咪替丁的计算pA2值分别为8.45±0.20、7.73±0.21和6.81±0.15。这些结果与在离体心脏制剂和体内胃分泌方面报道的拮抗剂的药理效力一致。因此,抑制胃细胞中组胺敏感的腺苷酸环化酶可能代表了一种用于体外评估H2受体拮抗剂的额外手段。