Konturek S J, Brzozowski T, Radecki T, Piastucki I
Scand J Gastroenterol Suppl. 1982;72:255-9.
This study compared the effects of pirenzepine, a novel selective antimuscarinic agent, and PGE2 applied topically on the gastric mucosa or parenterally on gastric secretion and formation of ASA and ethanol-induced gastric ulcerations in rats. Pirenzepine given topically in nonantisecretory dose prevented the formation of gastric ulcerations induced by ASA + 0.15 M HCl and absolute ethanol. These cytoprotective effects were comparable to those observed after PGE2 administered intragastrically or subcutaneously. Pirenzepine did not affect ulcer formation by ASA combined with 0.30 M HCl, whereas PGE2 was fully effective under these conditions. The cytoprotective action of pirenzepine was not accompanied by any change in the mucosal generation of PGs, indicating that endogenous PGs do not contribute to the cytoprotective property of this agent.
本研究比较了新型选择性抗毒蕈碱剂哌仑西平和局部应用于胃黏膜或经胃肠外途径应用于大鼠胃分泌以及阿司匹林和乙醇诱导的胃溃疡形成的前列腺素E2(PGE2)的作用。以非抗分泌剂量局部给予哌仑西平可预防由阿司匹林+0.15M盐酸和无水乙醇诱导的胃溃疡形成。这些细胞保护作用与胃内或皮下给予PGE2后观察到的作用相当。哌仑西平不影响阿司匹林与0.30M盐酸联合诱导的溃疡形成,而在此条件下PGE2完全有效。哌仑西平的细胞保护作用并未伴随黏膜前列腺素生成的任何变化,这表明内源性前列腺素对该药物的细胞保护特性没有贡献。