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兰索拉唑和奥美拉唑对大鼠胃中的血浆胃泌素水平、肠嗜铬样细胞、胃泌素细胞和生长抑素细胞具有相似的作用。

Lansoprazole and omeprazole have similar effects on plasma gastrin levels, enterochromaffin-like cells, gastrin cells and somatostatin cells in the rat stomach.

作者信息

Lee H, Håkanson R, Karlsson A, Mattsson H, Sundler F

机构信息

Gastrointestinal Pharmacology, Preclinical Research and Development, Astra Hässle AB, Mölndal, Sweden.

出版信息

Digestion. 1992;51(3):125-32. doi: 10.1159/000200887.

Abstract

This study compares the effects of lansoprazole and omeprazole on the activation and proliferation of enterochromaffin-like (ECL) cells in the rat stomach. Lansoprazole was given orally once daily for 10 weeks in two doses, 135 and 200 mumol/kg. Omeprazole was given by the same regimen in a dose of 400 mumol/kg, which is equipotent in terms of acid inhibition to the higher lansoprazole dose. Lansoprazole (both doses) as well as omeprazole raised the plasma gastrin levels about 11-fold 2 h after dosing and 8-to 10-fold 24 h after dosing, reflecting complete (2 h) and 70-80% (24 h) reductions of gastric acid secretion. Administration of either drug for 10 weeks increased the weight of the stomach and the oxyntic mucosa. The oxyntic mucosal histidine decarboxylase activity, histamine concentration and ECL cell density were increased to the same extent in the rats given either of the two lansoprazole doses or omeprazole. The numbers of antral gastrin cells were doubled and the numbers of antral somatostatin cells half that in the controls. These results show that long-standing lansoprazole-evoked hypergastrinemia affects the ECL cell similarly to omeprazole, ranitidine and other acid secretion inhibitors.

摘要

本研究比较了兰索拉唑和奥美拉唑对大鼠胃中肠嗜铬样(ECL)细胞激活和增殖的影响。兰索拉唑以两种剂量(135和200μmol/kg)每日口服一次,共给药10周。奥美拉唑按相同给药方案,以400μmol/kg的剂量给药,该剂量在抑酸方面与较高剂量的兰索拉唑等效。给药2小时后,兰索拉唑(两种剂量)以及奥美拉唑均使血浆胃泌素水平升高约11倍,给药24小时后升高8至10倍,这反映出胃酸分泌在给药2小时后完全减少(100%),在给药24小时后减少70 - 80%。两种药物给药10周均增加了胃和泌酸黏膜的重量。给予两种兰索拉唑剂量之一或奥美拉唑的大鼠,其泌酸黏膜组氨酸脱羧酶活性、组胺浓度和ECL细胞密度均有相同程度的增加。胃窦胃泌素细胞数量增加一倍,胃窦生长抑素细胞数量为对照组的一半。这些结果表明,长期由兰索拉唑引起的高胃泌素血症对ECL细胞的影响与奥美拉唑、雷尼替丁及其他胃酸分泌抑制剂相似。

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