Ruiz M C, Acosta A, Abad M J, Michelangeli F
Laboratorio de Fisiologia Gastrointestinal, Instituto Venezolano de Investigaciones Cientificas, Caracas.
Am J Physiol. 1993 Nov;265(5 Pt 1):G934-41. doi: 10.1152/ajpgi.1993.265.5.G934.
Pepsinogen and HCl secretion in the amphibian stomach are performed by a single cell type, the oxyntopeptic cell. These functions were studied in gastric mucosae of toads (Bufo marinus) mounted in Ussing-type chambers. HCl and peptic activity of luminal fluid were measured by titration and proteolysis of albumin, respectively. Distribution of pepsinogen in the gastric mucosa was heterogeneous, activity being highest in the proximal part of the stomach. Zymogen granules in the oxyntopeptic cell were more abundant in the deeper cells of the glands and in the fundus. On stimulation, the granules were released into the lumen of the glands by exocytosis. Histamine, forskolin, or carbachol alone each induced an increase in HCl and pepsinogen secretion. Carbachol after maximal histamine or forskolin stimulation produced an extra increase in both secretions that was greater for pepsinogen response. Similarly, joint addition of carbachol and histamine was more potent than histamine alone for both parameters; however, the effect was greater on pepsinogen release. Pretreatment with cimetidine blocked HCl and pepsinogen responses to carbachol but did not affect responses to forskolin. Addition of omeprazole to forskolin-stimulated mucosae uncoupled the two secretions, inducing a total inhibition of HCl secretion with a slight reduction in pepsinogen secretion. Thus pepsinogen release, similar to HCl secretion, is sensitive to cAMP and Ca(2+)-dependent secretagogues. However, the action of Ca2+ would require the previous elevation of cAMP induced by the different secretagogues. In such a case, the increase in intracellular Ca2+ would result in a nonparallel activation of the two secretions.
在两栖动物的胃中,胃蛋白酶原和盐酸的分泌由单一细胞类型即泌酸胃酶细胞来完成。这些功能在置于尤斯灌流小室中的蟾蜍(海蟾蜍)胃黏膜中进行了研究。分别通过白蛋白的滴定和蛋白水解来测定腔内液体的盐酸和胃蛋白酶活性。胃蛋白酶原在胃黏膜中的分布是不均匀的,活性在胃的近端部分最高。泌酸胃酶细胞中的酶原颗粒在腺体较深层的细胞和胃底中更为丰富。受到刺激时,颗粒通过胞吐作用释放到腺腔内。单独使用组胺、福斯高林或卡巴胆碱均可诱导盐酸和胃蛋白酶原分泌增加。在组胺或福斯高林最大刺激后加入卡巴胆碱,会使两种分泌额外增加,其中胃蛋白酶原反应增加得更多。同样,卡巴胆碱和组胺联合使用对这两个参数的作用比单独使用组胺更强;然而,对胃蛋白酶原释放的影响更大。用西咪替丁预处理可阻断盐酸和胃蛋白酶原对卡巴胆碱的反应,但不影响对福斯高林的反应。在福斯高林刺激的黏膜中加入奥美拉唑可使两种分泌解偶联,导致盐酸分泌完全抑制,胃蛋白酶原分泌略有减少。因此,胃蛋白酶原的释放与盐酸分泌一样,对环磷酸腺苷(cAMP)和钙(Ca2+)依赖性促分泌剂敏感。然而,Ca2+的作用需要由不同促分泌剂诱导的cAMP先升高。在这种情况下,细胞内Ca2+的增加将导致两种分泌的非平行激活。