Patel A V, Santani D D, Goyal R K
Department of Pharmacology, L. M. College of Pharmacy, Ahmedabad.
Indian J Physiol Pharmacol. 2000 Jul;44(3):350-4.
The present study was undertaken to investigate the mechanism of cytoprotective effects of magaldrate in aspirin plus pylorus-ligation model and ethanol-induced gastric ulcer model in rats. Magaldrate (60 mg/kg, p.o.) produced a significant reduction in the ulcer index and significant increase in mucus content in ethanol-induced gastric ulceration in rats. In aspirin plus pylorus-ligation model magaldrate produced significant decrease in ulcer index, total acidity and protein content (PR). It did not produce any significant change in volume of gastric secretion. However, it produced significant increase in total carbohydrate (TC) level but not in ratio between TC and proteins. It also produced a significant decrease in lipid peroxidation (as expressed by thiobarbituric acid reactive substance). Our data suggests the cytoprotective action of magaldrate on gastric mucosal cells which may be due to protection of gastric mucosa from lipid peroxidation.
本研究旨在探讨铝镁加在阿司匹林加幽门结扎模型和乙醇诱导的大鼠胃溃疡模型中的细胞保护作用机制。铝镁加(60mg/kg,口服)可显著降低乙醇诱导的大鼠胃溃疡模型的溃疡指数,并显著增加黏液含量。在阿司匹林加幽门结扎模型中,铝镁加可显著降低溃疡指数、总酸度和蛋白质含量(PR)。它对胃液分泌量没有产生任何显著变化。然而,它可显著提高总碳水化合物(TC)水平,但对TC与蛋白质的比值没有影响。它还可显著降低脂质过氧化(以硫代巴比妥酸反应性物质表示)。我们的数据表明铝镁加对胃黏膜细胞具有细胞保护作用,这可能是由于保护胃黏膜免受脂质过氧化的影响。