Gurll N J, Zinner M J, Callahan W
Gastroenterology. 1977 Aug;73(2):255-9.
Prevention of acute gastric erosions with histamine H2-receptor blocking agents suggests that these drugs may improve the ability of the gastric mucosa to maintain electrical, ionic, and protein concentration gradients. In 5 awake mongrel dogs, transmural potential difference, ion fluxes, and protein loss were measured across Heidenhain pouches topically exposed to isotonic solutions containing either 80 mM HCl or 80 mM HCl plus 20 mM sodium taurocholate (BS). The dogs received an intravenous infusion of either saline (as a control) or the H2 antagonist metiamide, 10 mumoles per kg-hr. Metiamide increased the H+ clearance rate found after acid test solution exposure but had no significant effect on potential difference or ion fluxes. H2 antagonism decreased the protein loss but not the increase in cation permeability due to BS. Net H+ loss actually increased, which, along with a decrease in Cl- gain, suggests inhibition of acid secretion by metiamide in BS-exposed gastric mucosa. These effects of metiamide point to histamine as a likely mediator of the gastric mucosal damage due to BS.
用组胺H2受体阻断剂预防急性胃糜烂表明,这些药物可能会提高胃黏膜维持电、离子和蛋白质浓度梯度的能力。在5只清醒的杂种犬中,测量了跨海德汉袋的跨壁电位差、离子通量和蛋白质损失,该袋局部暴露于含有80 mM HCl或80 mM HCl加20 mM牛磺胆酸钠(BS)的等渗溶液中。这些犬接受静脉输注生理盐水(作为对照)或H2拮抗剂甲硫米特,剂量为每千克每小时10微摩尔。甲硫米特增加了暴露于酸测试溶液后发现的H+清除率,但对电位差或离子通量没有显著影响。H2拮抗作用减少了蛋白质损失,但没有减少由于BS导致的阳离子通透性增加。净H+损失实际上增加了,这与Cl-摄取减少一起,表明甲硫米特对暴露于BS的胃黏膜的酸分泌有抑制作用。甲硫米特的这些作用表明组胺可能是BS导致胃黏膜损伤的介质。