Segawa K, Nakazawa S, Naito Y, Imai K, Kachi T, Tsukamoto S, Kajikawa M, Aichi M, Kimoto E, Sano H, Tominaga J, Ichikawa T, Oida T, Yoshino T
Gastroenterol Jpn. 1979 Dec;14(6):539-44. doi: 10.1007/BF02773712.
The suppressive effect of histamine H2-receptor antagonist, cimetidine, on gastric secretion was investigated in Ghosh-Schild rat. The study above was done in basal state under infusing normal saline (1 ml/h) and stimulated state by histamine-di-chloride (3.5 mg/kg-h), tetragastrin (50 mcg/kg-h) or calcium chloride (4 mg/kg-h). Dose related increase of cimetidine (1.7, 3.5, 7.0 and 14.0 mg/kg-h) were observed and correlated with the degree of inhibition of acid secretion. Cimetidine had a potent inhibitory activity on either basal and stimulated acid output by the agents above. Basal acid secretion was completely abolished by 3.5 mg/kg-h of cimetidine to the level of anacidity. The degree of inhibition by the same dose of cimetidine was different among the agents used as stimulant on acid secretion and it followed in the order of calcium, gastrin and histamine subsequently. This study indicated that histamine H2-receptor participated the gastric secretion induced by either gastrin or calcium other than histamine itself. This fact indicated the important role of endogenous histamine in gastric secretion induced by calcium and gastrin.
在戈什-希尔德大鼠中研究了组胺H2受体拮抗剂西咪替丁对胃酸分泌的抑制作用。上述研究在基础状态下进行,持续输注生理盐水(1毫升/小时),并在组胺二盐酸盐(3.5毫克/千克·小时)、四肽胃泌素(50微克/千克·小时)或氯化钙(4毫克/千克·小时)刺激状态下进行。观察到西咪替丁剂量相关的增加(1.7、3.5、7.0和14.0毫克/千克·小时),且与胃酸分泌抑制程度相关。西咪替丁对上述药物引起的基础胃酸分泌和刺激胃酸分泌均有强效抑制活性。3.5毫克/千克·小时的西咪替丁可使基础胃酸分泌完全消除至无酸水平。相同剂量的西咪替丁对用作胃酸分泌刺激剂的不同药物的抑制程度不同,顺序依次为钙、胃泌素和组胺。该研究表明,组胺H2受体参与了胃泌素或钙诱导的胃酸分泌,而非组胺本身。这一事实表明内源性组胺在钙和胃泌素诱导的胃酸分泌中起重要作用。