Giugliano D, Quatraro A, Consoli G, Ceriello A, Torella R, D'Onofrio F
Metabolism. 1987 Mar;36(3):286-9. doi: 10.1016/0026-0495(87)90190-9.
The administration of the long-acting met-enkephalin analogue (FK 33-824, Sandoz; Basel Switzerland) inhibits insulin secretion induced by glucose (oral and intravenous) and nonglucose (arginine and breakfast) secretagogues in both normal subjects and in patients with noninsulin-dependent diabetes mellitus. The plasma glucose rise triggered by oral glucose and breakfast is reduced by FK in both groups of subjects, suggesting for the opioid peptide an effect in delaying glucose absorption. The data suggest a negative role for enkephalin in the regulation of insulin secretion in both normal and noninsulin-dependent diabetic subjects.
长效甲硫氨酸脑啡肽类似物(FK 33 - 824,瑞士巴塞尔山德士公司)的给药可抑制正常受试者和非胰岛素依赖型糖尿病患者由葡萄糖(口服和静脉注射)以及非葡萄糖(精氨酸和早餐)促分泌剂诱导的胰岛素分泌。在两组受试者中,FK均可降低口服葡萄糖和早餐引发的血浆葡萄糖升高,提示该阿片肽具有延迟葡萄糖吸收的作用。这些数据表明,脑啡肽在正常和非胰岛素依赖型糖尿病受试者的胰岛素分泌调节中起负性作用。