Suppr超能文献

组胺释放剂对离体牛蛙胃黏膜胃酸分泌的影响。

Influence of histamine releasing agents on gastric acid secretion of isolated bullfrog gastric mucosa.

作者信息

Goto Y, Watanabe H Y, Watanabe K

出版信息

Jpn J Pharmacol. 1976 Dec;26(6):661-8. doi: 10.1254/jjp.26.661.

Abstract

The influence of histamine releasing agents on gastric acid secretion was studied in isolated bullfrog gastric mucosa preparations. Maximum acid secretory responses in our preparations were obtained by stimulation with tetragastrin (5 X 10(-7) g/ml), histamine (1 X 10(-5) g/ml) and bethanechol (1 X 10(-6) g/ml). Compound 48/80 (1 X 10(-4) g/ml) showed a transient stimulatory action which was followed by a gradual depression of basal acid secretion. The stimulatory phase of compound 48/80 was completely antagonized by burimamide (1 X 10(-5) g/ml), a histamine H2-receptor antagonist. In gastric mucosa preincubated with compound 48/80, the secretagogue action of tetragastrin or bethanechol was not exerted, although this preparation continued to respond to histamine. The effects of Triton X-100, decylamine and polymixin B were quite similar to those of compound 48/80. After pretreatment with compound 48/80, the gastric mucosa preparation became refractory to the stimulatory action of compound 48/80 or Triton X-100. It is thus suggested that endogenous histamine may play an important role in the secretagogue action of tetragastrin and bethanechol.

摘要

在分离的牛蛙胃黏膜制剂中研究了组胺释放剂对胃酸分泌的影响。在我们的制剂中,用四肽胃泌素(5×10⁻⁷克/毫升)、组胺(1×10⁻⁵克/毫升)和氨甲酰甲胆碱(1×10⁻⁶克/毫升)刺激可获得最大酸分泌反应。化合物48/80(1×10⁻⁴克/毫升)表现出短暂的刺激作用,随后基础酸分泌逐渐降低。组胺H₂受体拮抗剂布立马胺(1×10⁻⁵克/毫升)完全拮抗了化合物48/80的刺激阶段。在用化合物48/80预孵育的胃黏膜中,四肽胃泌素或氨甲酰甲胆碱的促分泌作用未发挥,尽管该制剂仍对组胺有反应。Triton X - 100、癸胺和多粘菌素B的作用与化合物48/80的作用非常相似。用化合物48/80预处理后,胃黏膜制剂对化合物48/80或Triton X - 100的刺激作用变得不敏感。因此提示内源性组胺可能在四肽胃泌素和氨甲酰甲胆碱的促分泌作用中起重要作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验