Gerber J G, Payne N A
Division of Clinical Pharmacology and Toxicology, University of Colorado Health Sciences Center, Denver, USA.
J Pharmacol Exp Ther. 1996 Nov;279(2):718-23.
The effect of secretin on pentagastrin- and gastrin-stimulated gastric histamine release and acid secretion was examined in the anesthetized dog model, where all compounds were infused directly into the artery supplying the gastric corpus. Secretin at an infusion rate of 10 ng/kg/min resulted in approximately 90% inhibition of gastric secretion in response to pentagastrin (20 ng/kg/min), whereas at the physiological postprandial concentration of 40 pg/ml it inhibited gastric secretion by approximately 55%. Gastric acid stimulated by gastrin I at the physiological post-prandial concentration of 150 pg/ml was inhibited by secretin at 40 pg/ml by approximately 80%. Pentagastrin stimulated histamine release to a peak of 168 +/- 34 ng/min, which was inhibited to 14 +/- 8 ng/min with the high concentration of secretin and to 85 +/- 21 ng/min at 40 pg/ml secretin. Gastrin I (150 pg/ml) stimulated histamine release to a peak of 10.6 +/- 4.6 ng/min, which was inhibited to 2.1 +/- 0.5 ng/min by secretin (40 pg/ml). Because secretin has been reported to stimulate gastric somatostatin release, we examined the somatostatin secretory rate concomitant with histamine release. Both doses of secretin stimulated gastric somatostatin release, compared with pentagastrin alone. The present data demonstrate that secretin, even at physiological concentrations, can inhibit gastric acid secretion in response to gastrin/pentagastrin, and one of the mechanisms of inhibition involves modulation of gastric histamine release. This effect of secretin on histamine release may be either direct, at the histamine-containing endocrine cells, or indirect, through somatostatin release.
在麻醉犬模型中,研究了促胰液素对五肽胃泌素和胃泌素刺激的胃组胺释放及胃酸分泌的影响,所有化合物均直接注入供应胃体的动脉。以10 ng/kg/min的输注速率输注促胰液素,可使对五肽胃泌素(20 ng/kg/min)的胃酸分泌抑制约90%,而在生理餐后浓度40 pg/ml时,可使胃酸分泌抑制约55%。在生理餐后浓度150 pg/ml时,促胰液素(40 pg/ml)可使胃泌素I刺激的胃酸分泌抑制约80%。五肽胃泌素刺激组胺释放至峰值168±34 ng/min,高浓度促胰液素可使其抑制至14±8 ng/min,40 pg/ml促胰液素可使其抑制至85±21 ng/min。胃泌素I(150 pg/ml)刺激组胺释放至峰值10.6±4.6 ng/min,促胰液素(40 pg/ml)可使其抑制至2.1±0.5 ng/min。由于已有报道促胰液素可刺激胃生长抑素释放,因此我们检测了与组胺释放同时的生长抑素分泌率。与单独使用五肽胃泌素相比,两种剂量的促胰液素均刺激胃生长抑素释放。目前的数据表明,促胰液素即使在生理浓度下,也能抑制胃泌素/五肽胃泌素刺激的胃酸分泌,其抑制机制之一涉及对胃组胺释放的调节。促胰液素对组胺释放的这种作用可能是直接的,作用于含组胺的内分泌细胞,也可能是间接的,通过生长抑素释放来实现。