Mineo H, Iwaki N, Onaga T, Kato S
Department of Veterinary Medicine, Rakuno Gakuen University, Hokkaido, Japan.
Res Vet Sci. 1994 May;56(3):298-302. doi: 10.1016/0034-5288(94)90145-7.
The effects of cholecystokinin-8 (CCK-8) and pentagastrin on insulin and glucagon secretion were studied in conscious sheep. Intravenous infusions of CCK-8 (3 to 1000 pmol kg-1 min-1 for 30 minutes) induced a dose-dependent increase in plasma insulin, but did not alter plasma glucagon concentration. The threshold dose of CCK-8 for stimulation of insulin secretion was 10 to 30 pmol kg-1 min-1. Pentagastrin was infused intravenously at doses of 10 to 3000 pmol kg-1 min-1. The maximal dose of pentagastrin slightly stimulated insulin, but not glucagon, secretion. The insulin secretory activity of pentagastrin was only 1/300 that of CCK-8 on a molar basis. The threshold dose of CCK-8 for stimulation of insulin secretion was similar to that for exocrine pancreatic secretion obtained in earlier studies. In conclusion, CCK is a potential candidate as a physiological factor regulating insulin secretion in sheep.
在清醒绵羊中研究了胆囊收缩素-8(CCK-8)和五肽胃泌素对胰岛素和胰高血糖素分泌的影响。静脉输注CCK-8(3至1000 pmol kg-1 min-1,持续30分钟)可引起血浆胰岛素呈剂量依赖性增加,但不改变血浆胰高血糖素浓度。刺激胰岛素分泌的CCK-8阈值剂量为10至30 pmol kg-1 min-1。以10至3000 pmol kg-1 min-1的剂量静脉输注五肽胃泌素。五肽胃泌素的最大剂量轻微刺激胰岛素分泌,但不刺激胰高血糖素分泌。以摩尔为基础,五肽胃泌素的胰岛素分泌活性仅为CCK-8的1/300。刺激胰岛素分泌的CCK-8阈值剂量与早期研究中获得的外分泌性胰腺分泌的阈值剂量相似。总之,CCK是调节绵羊胰岛素分泌的生理因子的潜在候选者。