Schäfer R, Schatz H
Acta Endocrinol (Copenh). 1979 Jul;91(3):493-500. doi: 10.1530/acta.0.0910493.
(Pro-)Insulin biosynthesis ([3H]leucine incorporation) and insulin secretion were studied in collagenase-isolated rat islets incubated for 3 hours at 1 and 2 mg/ml glucose in the presence of gastric inhibitory polypeptide (GIP). GIP augmented [3H]leucine incorporation and release of insulin at both glucose concentrations. In a second series of experiments it was found that an amino acid mixture was without influence on the insulotrophic action of GIP. Combined stimulation of insulin release by GIP and glucagon did not result in higher insulin output than observed in the presence of each substance alone. Thus GIP, in constrast to many other gastrointestinal peptides, however similar to glucagon, enhances not only release but also biosynthesis of insulin. This insulinotrophic action can be observed already at a glucose concentration of 1 mg/ml. The results underline the outstanding role which GIP appears to play in the regulation of beta-cell function.
在胃抑制性多肽(GIP)存在的情况下,研究了胶原酶分离的大鼠胰岛在1毫克/毫升和2毫克/毫升葡萄糖浓度下孵育3小时的(前)胰岛素生物合成([3H]亮氨酸掺入)和胰岛素分泌。在这两种葡萄糖浓度下,GIP均增加了[3H]亮氨酸掺入和胰岛素释放。在第二系列实验中发现,氨基酸混合物对GIP的促胰岛素作用没有影响。GIP和胰高血糖素联合刺激胰岛素释放,其胰岛素输出量并不比单独存在每种物质时更高。因此,与许多其他胃肠肽不同,但与胰高血糖素相似,GIP不仅能增强胰岛素释放,还能增强胰岛素生物合成。这种促胰岛素作用在葡萄糖浓度为1毫克/毫升时就已能观察到。这些结果强调了GIP在β细胞功能调节中似乎发挥的突出作用。