Sakamoto Y, Ide Y, Minami N, Tajima N, Yamada H
Nihon Naibunpi Gakkai Zasshi. 1977 Jul 20;53(7):833-43. doi: 10.1507/endocrine1927.53.7_833.
This study was performed in order to evaluate the effects of somatostatin on insulin releasing mechanisms and on glucose uptake in peripheral tissues using isolated pancreatic islets, isolated rat diaphragms and epididymal fat pads. Insulin release by various concentrations of glucose were examined, and it was found that 100 ng/ml of somatostatin significantly inhibited insulin release at the glucose concentration of 200 mg/dl. Somatostatin also significantly inhibted insulin release by the administration of 5microgram/ml of glucagon with 200 mg/dl of glucose concentration and 20 mM of orginine with 200mg/dl of glucose concentrations. But at the glucose concentration of 50mg/dl, no significant inhibition of somatostatin on insulin release was observed even when various concentrations of glucagon or arginine were added. The influence of somatostatin on peripheral tissues was examined in vitro, and no significant change on glucose uptake compared with the control group was shown in either tissues. The results indicated that somatostatin directly inhibited insulin release from rat pancreatic islets but had no effect on glucose uptake in peripheral tissues. The inhibitory effect of somatostatin on insulin release may act through the common mechanism of both glucose and other substances in leading to insulin release.
本研究旨在利用分离的胰岛、分离的大鼠膈肌和附睾脂肪垫,评估生长抑素对胰岛素释放机制及外周组织葡萄糖摄取的影响。检测了不同浓度葡萄糖刺激下的胰岛素释放情况,结果发现,在葡萄糖浓度为200mg/dl时,100ng/ml的生长抑素可显著抑制胰岛素释放。生长抑素还可显著抑制在葡萄糖浓度为200mg/dl时给予5μg/ml胰高血糖素以及在葡萄糖浓度为200mg/dl时给予20mM精氨酸所诱导的胰岛素释放。但在葡萄糖浓度为50mg/dl时,即便添加不同浓度的胰高血糖素或精氨酸,也未观察到生长抑素对胰岛素释放有显著抑制作用。体外检测了生长抑素对外周组织的影响,结果显示,与对照组相比,两种组织的葡萄糖摄取均未出现显著变化。结果表明,生长抑素可直接抑制大鼠胰岛释放胰岛素,但对外周组织的葡萄糖摄取无影响。生长抑素对胰岛素释放的抑制作用可能是通过葡萄糖及其他导致胰岛素释放的物质的共同机制发挥作用的。