Owens D R, Vora J, Morris T, Luzio S, Ryder R E, Atiea J, Hayes T M
Br J Clin Pharmacol. 1986 Sep;22(3):325-9. doi: 10.1111/j.1365-2125.1986.tb02894.x.
The metabolic effects of glucagon leading to hyperglycaemia are well recognised. However, the spasmolytic properties of glucagon have only relatively recently been utilised in clinical medicine. The marked hyperglycaemia accompanying the smooth muscle relaxant action of glucagon has led to the development of smaller peptides derived from glucagon which may retain the spasmolytic effects without the metabolic consequences. This study compares the metabolic and hormonal response to one such peptide, glucagon-(1-21)-peptide, with the parent peptide glucagon. The results demonstrate that glucagon-(1-21)-peptide has no metabolic effects comparable to glucagon. In normal subjects and non-insulin dependent diabetics, glucagon-(1-21)-peptide has no stimulatory effect on the pancreatic beta-cell.
胰高血糖素导致高血糖的代谢作用已得到充分认识。然而,胰高血糖素的解痉特性直到最近才在临床医学中得到应用。伴随胰高血糖素平滑肌松弛作用出现的显著高血糖,促使人们研发出了源自胰高血糖素的较小肽段,这些肽段可能保留解痉作用而无代谢后果。本研究比较了一种此类肽段,即胰高血糖素-(1-21)-肽,与母体肽段胰高血糖素的代谢及激素反应。结果表明,胰高血糖素-(1-21)-肽没有与胰高血糖素相当的代谢作用。在正常受试者和非胰岛素依赖型糖尿病患者中,胰高血糖素-(1-21)-肽对胰腺β细胞没有刺激作用。