Stridsberg M, Sandler S, Wilander E
Department of Clinical Chemistry, Uppsala University, Sweden.
Regul Pept. 1993 Jun 11;45(3):363-70. doi: 10.1016/0167-0115(93)90362-c.
The aim of this work was to simultaneously study the secretion of islet amyloid polypeptide (IAPP) and insulin from isolated rat pancreatic islets in vitro. For examination of stimulated beta-cells, nutrient secretagogues (16.7 mM glucose, 10 mM leucine + 2 mM glutamine), phosphodiesterase inhibition (5 mM theophylline), a sulphonylurea (0.5 microgram/ml glipizide), a non-nutrient amino acid (10 mM arginine), cholinergic stimulation (0.1 mM carbamylcholine) and insulinotropic peptides (0.1 microM vasoactive intestinal polypeptide and 0.1 microM glucagon), were used. For beta-cell suppression glucose phosphorylation inhibition (10 mM mannoheptulose), depletion of extracellular calcium, activation of the ATP-regulated K(+)-channel (0.5 mM diazoxide), adrenoreceptor stimulation (3 microM adrenaline), paracrine modulation (0.1 microM somatostatin), short-term treatment with a selective beta-cytotoxin (1.1 and 2.2 mM streptozotocin) and long-term treatment with a cytokine (25 U/ml interleukin-1 beta), were studied. The compounds with known effects on insulin secretion exerted their expected actions and this was paralleled by similar relative changes, with a possible exception for glucagon, in the IAPP secretion. The ratio of IAPP/insulin released did not change significantly under any of the tested experimental conditions, except for a slight increase following carbamylcholine stimulation. On a molar basis approx. 1% of IAPP was released when compared with insulin. These results are consistent with the hypothesis that the regulation of IAPP secretion from beta-cells of isolated rat pancreatic islets is essentially regulated by the same mechanisms as insulin secretion.
这项工作的目的是在体外同时研究分离的大鼠胰岛中胰岛淀粉样多肽(IAPP)和胰岛素的分泌。为了检测受刺激的β细胞,使用了营养促分泌剂(16.7 mM葡萄糖、10 mM亮氨酸 + 2 mM谷氨酰胺)、磷酸二酯酶抑制剂(5 mM茶碱)、磺酰脲类药物(0.5微克/毫升格列吡嗪)、非营养性氨基酸(10 mM精氨酸)、胆碱能刺激剂(0.1 mM氨甲酰胆碱)和促胰岛素肽(0.1 microM血管活性肠肽和0.1 microM胰高血糖素)。为了抑制β细胞,研究了葡萄糖磷酸化抑制(10 mM甘露庚酮糖)、细胞外钙耗竭、ATP调节的钾通道激活(0.5 mM二氮嗪)、肾上腺素能刺激(3 microM肾上腺素)、旁分泌调节(0.1 microM生长抑素)、选择性β细胞毒素的短期处理(1.1和2.2 mM链脲佐菌素)以及细胞因子的长期处理(25 U/ml白细胞介素-1β)。对胰岛素分泌有已知作用的化合物发挥了预期作用,并且在IAPP分泌中也出现了类似的相对变化,胰高血糖素可能除外。在任何测试的实验条件下,IAPP/胰岛素释放的比率均未发生显著变化,氨甲酰胆碱刺激后略有增加除外。以摩尔为基础,与胰岛素相比,约1%的IAPP被释放。这些结果与以下假设一致,即分离的大鼠胰岛β细胞中IAPP分泌的调节基本上受与胰岛素分泌相同的机制调控。