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大鼠胃酸分泌抑制、血浆胃泌素与胃底黏膜组氨酸脱羧酶活性之间的相关性

Correlation between inhibition of gastric acid secretion, plasma gastrin, and oxyntic mucosal histidine decarboxylase activity in the rat.

作者信息

Ryberg B, Mattsson H, Larsson H, Carlsson E

机构信息

Dept. of Biology, AB Hässle, Mölndal, Sweden.

出版信息

Scand J Gastroenterol. 1989 Apr;24(3):287-92. doi: 10.3109/00365528909093048.

Abstract

Female rats were treated for 1 week with ranitidine (125-1700 mumol/kg.day, given subcutaneously by means of osmotic minipumps), the proton pump inhibitor omeprazole (10-400 mumol/kg.day orally), or vehicle. Acid secretion, plasma gastrin levels, and oxyntic mucosal histidine decarboxylase (HDC) activity were determined. Both compounds dose-dependently inhibited maximally stimulated gastric acid secretion and caused a parallel increase in plasma gastrin levels. There was very good correlation between plasma gastrin levels and HDC activity for both compounds, although higher oxyntic mucosal HDC activity was found during ranitidine treatment. The higher HDC activity in the ranitidine-treated rats indicated the presence of a histamine H2-receptor on the ECL cells. It is concluded that, regardless of what kind of antisecretory agent is used, a dose-dependent inhibition of gastric acid secretion results in a parallel increase in plasma levels of gastrin, and as a consequence the HDC activity in the rat oxyntic mucosa is increased.

摘要

给雌性大鼠用雷尼替丁(125 - 1700微摩尔/千克·天,通过渗透微型泵皮下给药)、质子泵抑制剂奥美拉唑(10 - 400微摩尔/千克·天,口服)或赋形剂处理1周。测定胃酸分泌、血浆胃泌素水平和胃黏膜组胺脱羧酶(HDC)活性。两种化合物均剂量依赖性地抑制最大刺激胃酸分泌,并导致血浆胃泌素水平平行升高。两种化合物的血浆胃泌素水平与HDC活性之间存在非常良好的相关性,尽管在雷尼替丁治疗期间发现胃黏膜HDC活性较高。雷尼替丁治疗的大鼠中较高的HDC活性表明肠嗜铬样细胞(ECL细胞)上存在组胺H2受体。得出的结论是,无论使用何种抗分泌剂,胃酸分泌的剂量依赖性抑制都会导致血浆胃泌素水平平行升高,结果大鼠胃黏膜中的HDC活性增加。

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