Ishizuka J, Tatemoto K, Cohn D V, Thompson J C, Greeley G H
Department of Surgery, University of Texas Medical Branch, Galveston.
Regul Pept. 1991 Jun 11;34(1):25-32. doi: 10.1016/0167-0115(91)90221-2.
The effects of porcine pancreastatin on insulin release stimulated by insulinotropic agents, glucagon, cholecystokinin-octapeptide (CCK-8), gastric inhibitory polypeptide (GIP) and L-arginine, were compared to those of bovine chromogranin A (CGA) using the isolated perfused rat pancreas. Pancreastatin significantly potentiated glucagon-stimulated insulin release (first phase: 12.5 +/- 0.9 ng/8 min; second phase: 34.5 +/- 1.6 ng/25 min in controls; 16.5 +/- 1.1 ng/8 min and 44.0 +/- 2.2 ng/25 min in pancreastatin group), whereas CGA was ineffective. The first phase of L-arginine-stimulated insulin release was also potentiated by pancreastatin (6.9 +/- 0.5 ng/5 min in controls, 8.4 +/- 0.6 ng/5 min in pancreastatin group), but not by CGA. Pancreastatin did not affect CCK-8 or GIP-stimulated insulin release. Similarly, CGA did not affect insulin release stimulated by CCK-8 or GIP. These findings suggest that pancreastatin stimulates insulin release in the presence of glucagon. Because pancreastatin can have multiple effects on insulin release, which are dependent upon the local concentration of insulin effectors, pancreastatin may participate in the fine tuning of insulin release from B cells.
利用离体灌注大鼠胰腺,比较了猪胰抑制素对促胰岛素分泌剂、胰高血糖素、八肽胆囊收缩素(CCK - 8)、胃抑制多肽(GIP)和L - 精氨酸刺激的胰岛素释放的影响,以及牛嗜铬粒蛋白A(CGA)的影响。胰抑制素显著增强了胰高血糖素刺激的胰岛素释放(第一阶段:对照组为12.5±0.9 ng/8分钟;第二阶段:对照组为34.5±1.6 ng/25分钟;胰抑制素组为16.5±1.1 ng/8分钟和44.0±2.2 ng/25分钟),而CGA则无效。胰抑制素也增强了L - 精氨酸刺激的胰岛素释放的第一阶段(对照组为6.9±0.5 ng/5分钟,胰抑制素组为8.4±0.6 ng/5分钟),但CGA没有。胰抑制素不影响CCK - 8或GIP刺激的胰岛素释放。同样,CGA也不影响CCK - 8或GIP刺激的胰岛素释放。这些发现表明,胰抑制素在胰高血糖素存在的情况下刺激胰岛素释放。由于胰抑制素对胰岛素释放可能有多种作用,这取决于胰岛素效应物的局部浓度,胰抑制素可能参与了B细胞胰岛素释放的精细调节。