Furukawa O, Matsui H, Suzuki N
Department of Applied Pharmacology, Kyoto Pharmaceutical University, Japan.
Jpn J Pharmacol. 1997 Sep;75(1):21-5. doi: 10.1254/jjp.75.21.
We have established models of cell damage induced by acid and pepsin using rat gastric epithelial cells (RGM1). In the present study, the effects of aluminum hydroxide [Al(OH)3] and potassium sucrose octasulfate (KSOS), which are components of sucralfate, and sucralfate on cell damage and peptic activity of pepsin were examined. Pretreatment of cells with sucralfate (0.1-3 mg/ml) or Al(OH)3 (0.1-1 mg/ml) for 2 hr prevented both acid- (pH 4.0) and pepsin- (pH 4.5) induced cell damage. However, KSOS (0.1-1 mg/ml) did not show any effects on two different types of cell damage. The peptic activity of pepsin at pH 4.5 was about 10% of that at pH 2.0. Sucralfate and KSOS slightly inhibited peptic activity at pH 4.5. Al(OH)3 inhibited peptic activity by approximately 50%; however, no concentration-dependent pattern was observed. Pepstatin (0.003-0.1 mg/ml), a specific inhibitor of pepsin, inhibited the peptic activity in a concentration-dependent manner. Here, we confirmed that sucralfate and Al(OH)3 have cytoprotective effects against acid- and pepsin-induced cell damage. The mechanism behind the cytoprotective effects of sucralfate seems to relate to adhesion of the cell surface and neutralization of hydrogen ion by aluminum that prevents the penetration of hydrogen ions into the cells.
我们利用大鼠胃上皮细胞(RGM1)建立了酸和胃蛋白酶诱导的细胞损伤模型。在本研究中,检测了硫糖铝的成分氢氧化铝[Al(OH)₃]和蔗糖八硫酸钾(KSOS)以及硫糖铝对细胞损伤和胃蛋白酶消化活性的影响。用硫糖铝(0.1 - 3mg/ml)或氢氧化铝(0.1 - 1mg/ml)预处理细胞2小时可预防酸(pH 4.0)和胃蛋白酶(pH 4.5)诱导的细胞损伤。然而,KSOS(0.1 - 1mg/ml)对两种不同类型的细胞损伤均无影响。胃蛋白酶在pH 4.5时的消化活性约为pH 2.0时的10%。硫糖铝和KSOS在pH 4.5时轻微抑制消化活性。氢氧化铝抑制消化活性约50%;然而,未观察到浓度依赖性模式。胃蛋白酶的特异性抑制剂胃抑素(0.003 - 0.1mg/ml)以浓度依赖性方式抑制消化活性。在此,我们证实硫糖铝和氢氧化铝对酸和胃蛋白酶诱导的细胞损伤具有细胞保护作用。硫糖铝细胞保护作用的机制似乎与细胞表面的粘附以及铝对氢离子的中和有关,从而防止氢离子进入细胞。