Pederson R A, Schubert H E, Brown J C
Can J Physiol Pharmacol. 1975 Apr;53(2):217-23. doi: 10.1139/y75-032.
The effect of highly purified gastric inhibitory polypeptide (GIP) on immunoreactive insulin (IRI) secretion in the conscious fasted dog was investigated. Significant increases in IRI release were observed with intravenous administration of three different doses of GIP. These were accompanied by depression in fasting serum-glucose levels. Preliminary studies were undertaken to determine whether this insulinotropic action of GIP could be attributed to a particular segment of the GIP molecule. GIP fragments produced by cleavage with cyanogen bromide and trypsin showed no significant stimulation of IRI release. The possibility that GIP might itself enhance glucose uptake or potentiate insulin-induced glucose uptake was studied with the rat hemidiaphragm preparation. No such effect was observed. In the light of this and other recent work, it is concluded that GIP is a strong candidate for an active principle in the enteroinsular axis.
研究了高纯度胃抑制多肽(GIP)对清醒禁食犬免疫反应性胰岛素(IRI)分泌的影响。静脉注射三种不同剂量的GIP后,观察到IRI释放显著增加。同时空腹血清葡萄糖水平降低。进行了初步研究以确定GIP的这种促胰岛素作用是否可归因于GIP分子的特定片段。用溴化氰和胰蛋白酶切割产生的GIP片段未显示出对IRI释放的显著刺激。用大鼠半膈肌制备物研究了GIP本身可能增强葡萄糖摄取或增强胰岛素诱导的葡萄糖摄取的可能性。未观察到这种作用。鉴于此及其他近期研究工作,得出结论:GIP是肠胰岛轴中一种活性成分的有力候选者。