Beales Ian L P, Calam John
Gastrointestinal Research Unit, Department of Physiology and Cell Biology, School of Medicine, Health Policy and Practice, University of East Anglia, Norwich NR4 7TJ, United Kingdom.
BMC Physiol. 2003 Oct 22;3:13. doi: 10.1186/1472-6793-3-13.
Amylin (islet amyloid polypeptide) is a hormone with suggested roles in the regulation of glucose homeostasis, gastric motor and secretory function and gastroprotection. In the gastric mucosa amylin is found co-localised with somatostatin in D-cells. The factors regulating gastric amylin release are unknown. In this study we have investigated the regulation of amylin release from gastric mucosal cells in primary culture. Rabbit fundic mucosal cells enriched for D-cells by counterflow elutriation were cultured for 40 hours. Amylin and somatostatin release over 2 hours in response to agonists were assessed.
Amylin release was significantly enhanced by activation of protein kinase C with phorbol-12-myristate-13-acetate, adenylate cyclase with forskolin and elevation of intracellular calcium with A23187. Cholecystokinin (CCK), epinephrine and glucagon-like peptide-1 (GLP-1) each stimulated amylin release in a dose-dependent manner. Maximal CCK-stimulated release was greater than either epinephrine or GLP-1, even when the effects of the latter two were enhanced by isobutylmethylxanthine. Stimulated amylin release was significantly inhibited by carbachol (by 51-59%) and octreotide (by 33-42%). Somatostatin release paralleled that of amylin.
The cultured D-cell model provides a means of studying amylin release. Amylin secretion is stimulated by receptor-dependent and -independent activation of Ca2+/protein kinase C and adenylate cyclase pathways. Inhibition involves activation of muscarinic receptors and auto-regulation by somatostatin.
胰淀素(胰岛淀粉样多肽)是一种激素,在调节葡萄糖稳态、胃运动和分泌功能以及胃保护方面具有一定作用。在胃黏膜中,胰淀素与生长抑素共同定位于D细胞。调节胃胰淀素释放的因素尚不清楚。在本研究中,我们调查了原代培养的胃黏膜细胞中胰淀素释放的调节情况。通过逆流淘析富集D细胞的兔胃底黏膜细胞培养40小时。评估了激动剂作用2小时内胰淀素和生长抑素的释放情况。
佛波醇-12-肉豆蔻酸酯-13-乙酸酯激活蛋白激酶C、福斯可林激活腺苷酸环化酶以及A23187升高细胞内钙均能显著增强胰淀素释放。胆囊收缩素(CCK)、肾上腺素和胰高血糖素样肽-1(GLP-1)均以剂量依赖方式刺激胰淀素释放。即使异丁基甲基黄嘌呤增强了后两者的作用,CCK刺激的最大释放量仍大于肾上腺素或GLP-1。卡巴胆碱(抑制51 - 59%)和奥曲肽(抑制33 - 42%)可显著抑制刺激后的胰淀素释放。生长抑素的释放与胰淀素平行。
培养的D细胞模型为研究胰淀素释放提供了一种方法。胰淀素分泌受Ca2+/蛋白激酶C和腺苷酸环化酶途径的受体依赖性和非依赖性激活刺激。抑制作用涉及毒蕈碱受体的激活和生长抑素的自身调节。