Joost H G, Beckmann J, Lenzen S, Hasselblatt A
Acta Endocrinol (Copenh). 1976 May;82(1):121-6. doi: 10.1530/acta.0.0820121.
Cyproheptadine (1, 10 and 100 muM) significantly reduced insulin release from isolated mouse islets in response to glucose. In contrast, 1 mM cyproheptadine induced a large release of insulin into the incubation medium probably due to islet cell damage, since the islets had lost a considerable amount of their protein content. 3',5'-cyclic-AMP-levels of the islets were not significantly affected by 10 muM cyproheptadine in the presence as well as in the absence of theophylline (10 mM). As the inhibitory effect of cyproheptadine on insulin release was correlated with reduced accumulation of calcium-45, the agent may inhibit insulin release by interfering with the calcium handling of the beta-cell.
赛庚啶(1、10和100微摩尔)可显著降低分离的小鼠胰岛对葡萄糖的胰岛素释放。相比之下,1毫摩尔赛庚啶可能由于胰岛细胞损伤而导致大量胰岛素释放到孵育培养基中,因为胰岛损失了相当数量的蛋白质。在有或没有茶碱(10毫摩尔)存在的情况下,10微摩尔赛庚啶对胰岛的3',5'-环磷酸腺苷水平没有显著影响。由于赛庚啶对胰岛素释放的抑制作用与钙-45积累减少相关,该药物可能通过干扰β细胞的钙处理来抑制胰岛素释放。