Rhodes C J, Campbell I L, Szopa T M, Biden T J, Reynolds P D, Fernando O N, Taylor K W
Clin Sci (Lond). 1985 May;68(5):567-72. doi: 10.1042/cs0680567.
Beta-Cell function in human islets derived from a number of kidney donors was investigated by using various types of islet preparations. With fresh islets, both insulin release and biosynthesis were increased by raising glucose concentrations, although the response was a variable one. In fresh islets, the effects of 5 mmol of glucose/l on release were potentiated by 10 mmol of D-3-hydroxybutyrate/l. Insulin release at 20 mmol of glucose/l was inhibited by adrenaline (0.1 mmol/l), and potentiated by theophylline (10 mmol/l) in the presence of 5 mmol of glucose/l, in islets cultured for 4 days. After culture for 8 days, islets still showed an increase in insulin release and biosynthesis in response to glucose. Pancreas slices derived from fresh human tissue also responded to increasing concentrations of glucose with a sigmoidal curve for insulin release.
通过使用多种类型的胰岛制剂,对来自多名肾脏供体的人类胰岛中的β细胞功能进行了研究。对于新鲜胰岛,提高葡萄糖浓度可增加胰岛素释放和生物合成,尽管反应存在差异。在新鲜胰岛中,10 mmol/L的D-3-羟基丁酸可增强5 mmol/L葡萄糖对释放的作用。在培养4天的胰岛中,0.1 mmol/L的肾上腺素抑制20 mmol/L葡萄糖时的胰岛素释放,而在存在5 mmol/L葡萄糖的情况下,10 mmol/L的茶碱可增强该释放。培养8天后,胰岛对葡萄糖仍表现出胰岛素释放和生物合成增加。源自新鲜人体组织的胰腺切片对葡萄糖浓度升高的反应也呈胰岛素释放的S形曲线。