Simons M A, Moody F G, Torma M J
Gastroenterology. 1976 Oct;71(4):603-7.
The effects of topical application of carbenoxolone at neutral and acidic pH were compared in exteriorized, chambered segments of canine gastric corpus. When dissolved in saline at pH 7.5 to 8.0, 0.25% carbenoxolone caused a rapid drop in gastric potential difference of 56 +/- 2 mv and greatly increased permeability to H+ ions. Blood flow, as measured by radioactive microspheres, was not changed by carbenoxolone treatment, but subsequent exposure to isotonic HC1 caused an abrupt rise in flow. Application of 0.25% carbenoxolone suspension in isotonic HC1 caused no change in potential difference, permeability, or blood flow. Neither carbenoxolone preparation had a significant effect on aspirin-induced H+ back-diffusion or injury.
在犬胃体的外置腔段中,比较了在中性和酸性pH值下局部应用甘珀酸的效果。当在pH值为7.5至8.0的盐水中溶解时,0.25%的甘珀酸导致胃电位差迅速下降56±2毫伏,并大大增加了对H+离子的通透性。用放射性微球测量的血流量,在甘珀酸处理后没有改变,但随后暴露于等渗盐酸会导致血流量突然增加。在等渗盐酸中应用0.25%的甘珀酸悬浮液对电位差、通透性或血流量没有影响。两种甘珀酸制剂对阿司匹林诱导的H+反向扩散或损伤均无显著影响。