Schmidt C, Baumeister B, Kipnowski J, Miederer S E, Vetter H
Medical Policlinic, University of Bonn, Germany.
Hepatogastroenterology. 1998 Nov-Dec;45(24):2443-6.
BACKGROUND/AIMS: Prostaglandin E2 (PGE2) plays an important role in the inhibition of gastric acid production and exerts cytoprotective action. The in vitro and in vivo effect of magaldrate, an aluminum containing antacid, on PGE2 synthesis in the gastric mucosa was investigated.
In the first part of the study, magaldrate was added to a suspension of isolated gastric mucosal cells. In the second part, the antacid gel was applied to the gastric mucosa during gastroscopy and biopsies were taken from the same site 5 and 10 min later.
The antacid significantly stimulated PGE2 release from the suspension of isolated gastric cells in vitro. The biopsies obtained after the application of magaldrate showed an increased PGE2 production compared to specimens obtained before.
The data suggest that in addition to its neutralizing capacity as an antacid, magaldrate contributes to the cytoprotective activity of the mucosa by stimulating endogenous PGE2 synthesis.
背景/目的:前列腺素E2(PGE2)在抑制胃酸分泌中起重要作用,并具有细胞保护作用。研究了含铝抗酸剂氢氧化铝镁对胃黏膜中PGE2合成的体外和体内作用。
在研究的第一部分,将氢氧化铝镁添加到分离的胃黏膜细胞悬液中。在第二部分中,在胃镜检查期间将抗酸凝胶应用于胃黏膜,并在5分钟和10分钟后从同一部位取活检组织。
抗酸剂在体外显著刺激分离的胃细胞悬液中PGE2的释放。与应用氢氧化铝镁之前获得的标本相比,应用后获得的活检组织显示PGE2产生增加。
数据表明,除了作为抗酸剂的中和能力外,氢氧化铝镁还通过刺激内源性PGE2合成来促进黏膜的细胞保护活性。