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组胺及某些H2拮抗剂对胃“体外”分泌的作用

Action of histamine and of some H2-antagonists on gastric secretion 'in vitro'.

作者信息

Coruzzi G, Adami M, Bertaccini G

出版信息

Agents Actions. 1984 Apr;14(3-4):516-21. doi: 10.1007/BF01973862.

Abstract

The effect of histamine and of some H2-antagonists on isolated gastric mucosal preparation from immature (14-18 days) rats, was investigated. Basal secretion varied, in our experimental conditions, between 1.06 and 3.54 mumol cm-2 h-1, reaching higher values (approximately 4.6 mumol cm-2 h-1) only in a small percentage of animals (10%). Histamine exerted a concentration-dependent stimulation of acid secretion in concentrations varying between 2 X 10(-6) and 1.6 X 10(-4) M. The response to histamine was competitively antagonized by ranitidine (pA2 value = 6.78) and by 4(5)-(4- isopropylaminomethyleniminophenyl ) imidazole (compound marked DA 4577) (pA2 value = 7.37). Oxmetidine acted as a competitive antagonist only for concentrations as low as 10(-8) M; higher concentrations (10(-7) and 10(-6) M) determined a non-competitive inhibition. Ranitidine and compound marked DA 4577 did not affect basal secretion up to concentrations of 3 X 10(-4) M. On the contrary oxmetidine exerted a concentration-dependent inhibition starting from 10(-5) M. Since in our experimental conditions the role of calcium ions in the regulation of basal secretion could not be established, the mechanism of action of oxmetidine was not completely clarified, even if an interference in the utilization of calcium ions may be suggested. In any case it is deemed of interest that this H2-antagonist was the only compound capable of inducing a reversible complete inhibition of basal acid secretion (only KSCN, in very high concentrations, had a similar behaviour).

摘要

研究了组胺及一些H2拮抗剂对未成熟(14 - 18天)大鼠离体胃黏膜制剂的作用。在我们的实验条件下,基础分泌量在1.06至3.54 μmol·cm-2·h-1之间变化,仅在一小部分动物(10%)中达到较高值(约4.6 μmol·cm-2·h-1)。组胺在2×10(-6)至1.6×10(-4) M的浓度范围内对胃酸分泌产生浓度依赖性刺激。雷尼替丁(pA2值 = 6.78)和4(5)-(4 - 异丙基氨基亚甲基亚氨基苯基)咪唑(标记为DA 4577的化合物)(pA2值 = 7.37)对组胺的反应具有竞争性拮抗作用。奥美替丁仅在低至10(-8) M的浓度下作为竞争性拮抗剂起作用;较高浓度(10(-7)和10(-6) M)则产生非竞争性抑制。雷尼替丁和标记为DA 4577的化合物在浓度高达3×10(-4) M时不影响基础分泌。相反,奥美替丁从10(-5) M开始产生浓度依赖性抑制。由于在我们的实验条件下无法确定钙离子在基础分泌调节中的作用,奥美替丁的作用机制尚未完全阐明,尽管可能提示其对钙离子利用有干扰。无论如何,值得关注的是,这种H2拮抗剂是唯一能够诱导基础胃酸分泌可逆性完全抑制的化合物(只有高浓度的硫氰酸钾有类似行为)。

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