Vaysse N, Pradayrol L, Chayvialle J A, Pignal F, Esteve J P, Susini C, Descos F, Ribet A
Endocrinology. 1981 May;108(5):1843-7. doi: 10.1210/endo-108-5-1843.
The effects of somatostatin-14 (S14) and somatostatin-28 (S28), a novel intestinal peptide containing somatostatin tetradecapeptide in its C-terminal position, on the bombesin-stimulated release of gastrin, insulin, and glucagon were tested. On iv infusion of bombesin, the increase in the level of glucagon was seen to be twice that of gastrin, and the insulin increase was 8 times that of gastrin. Plasma concentrations of somatostatin were not modified. S14 and S28 inhibited the release of gastrin, insulin, and glucagon; insulin release was inhibited most effectively, with glucagon release next, and gastrin release least inhibited. Based on the exogenous dose needed to produce equal effects, S28 was more potent than S14 on a molar basis, but based on the plasma concentrations needed to produce equal effects, S14 and S28 were equipotent.
对生长抑素 -14(S14)和生长抑素 -28(S28,一种在其 C 末端含有生长抑素十四肽的新型肠肽)对蛙皮素刺激的胃泌素、胰岛素和胰高血糖素释放的影响进行了测试。静脉输注蛙皮素时,胰高血糖素水平的升高是胃泌素的两倍,胰岛素的升高是胃泌素的 8 倍。生长抑素的血浆浓度未发生改变。S14 和 S28 抑制胃泌素、胰岛素和胰高血糖素的释放;胰岛素释放受到的抑制最为有效,其次是胰高血糖素释放,胃泌素释放受到的抑制最小。基于产生同等效应所需的外源性剂量,按摩尔计算 S28 比 S14 更有效,但基于产生同等效应所需的血浆浓度,S14 和 S28 具有同等效力。