Steinert Robert E, Schirra Joerg, Meyer-Gerspach Anne C, Kienle Philipp, Fischer Heiko, Schulte Felix, Goeke Burkhard, Beglinger Christoph
From the Department of Biomedicine and Division of Gastroenterology, University Hospital Basel, Basel, Switzerland (RES, ACM-G, PK, HF, FS, and CB), and the Department of Internal Medicine II, Clinical Research Unit, Clinical Center of the Ludwig Maximilians University, Campus Grosshardern, Munich, Germany (JS and BG).
Am J Clin Nutr. 2014 Aug;100(2):514-23. doi: 10.3945/ajcn.114.083246. Epub 2014 Jun 25.
Exogenous glucagon-like peptide-1 (GLP-1) inhibits eating in healthy, overweight, and diabetic subjects.
The GLP-1 receptor antagonist exendin(9-39)NH2 (ex9-39) was used to further explore the role of GLP-1 as an endogenous satiation signal.
Two double-blind, 4-way crossover studies were performed, each of which included 10 healthy men. In study A, subjects received an intravenous infusion of ex9-39 or saline plus an oral glucose preload and an intraduodenal infusion of saline or glucose for 60 min. In study B, intravenous infusions were identical, but an oral mixed-liquid meal preload and a 60-min intraduodenal infusion of saline or oleic acid were administered. Thirty minutes after oral preloads, subjects ate and drank ad libitum, and amounts ingested and the time to meal completion were quantified. In addition, appetite and plasma GLP-1, peptide YY (PYY), insulin, glucagon, and blood glucose concentrations were measured.
In both studies, GLP-1, PYY, and glucagon were substantially higher with intravenous ex9-39 than with intravenous saline (P ≤ 0.001). Insulin was lower with intravenous ex9-39 during intraduodenal glucose (P ≤ 0.05). The decrease in prospective food consumption and desire to eat during ad libitum eating after glucose ingestion was slightly attenuated (P ≤ 0.05 and P ≤ 0.01, respectively) with ex9-39. However, with intravenous ex9-39, food and fluid intakes and eating duration were not changed in either study.
GLP-1 receptor antagonism slightly modulates appetite during ad libitum eating, but food and fluid intakes and meal duration remain unchanged, suggesting that endogenous GLP-1 is a weak satiation signal. However, concomitant substantial increases in plasma PYY and glucagon may counteract a desatiating effect of ex9-39. The effect of ex9-39 on PYY secretion supports an autoinhibitory feedback mechanism that controls L cell secretion; the effect on insulin and glucagon confirms the role of GLP-1 in glycemic control through its action on pancreatic α and β cells.
外源性胰高血糖素样肽-1(GLP-1)可抑制健康、超重及糖尿病受试者的进食。
使用GLP-1受体拮抗剂艾塞那肽(9-39)NH2(ex9-39)进一步探究GLP-1作为内源性饱腹感信号的作用。
进行了两项双盲、四向交叉研究,每项研究纳入10名健康男性。在研究A中,受试者接受静脉输注ex9-39或生理盐水,同时给予口服葡萄糖预负荷,并进行60分钟的十二指肠内输注生理盐水或葡萄糖。在研究B中,静脉输注相同,但给予口服混合液餐预负荷,并进行60分钟的十二指肠内输注生理盐水或油酸。口服预负荷30分钟后,受试者自由进食和饮水,对摄入的量和进食结束时间进行量化。此外,测量食欲以及血浆GLP-1、肽YY(PYY)、胰岛素、胰高血糖素和血糖浓度。
在两项研究中,静脉输注ex9-39时的GLP-1、PYY和胰高血糖素水平均显著高于静脉输注生理盐水时(P≤0.001)。十二指肠内输注葡萄糖期间,静脉输注ex9-39时胰岛素水平较低(P≤0.05)。ex9-39使葡萄糖摄入后自由进食期间预期食物消耗量和进食欲望的降低略有减弱(分别为P≤0.05和P≤0.01)。然而,在两项研究中,静脉输注ex9-39时食物和液体摄入量以及进食持续时间均未改变。
GLP-1受体拮抗作用在自由进食期间对食欲有轻微调节作用,但食物和液体摄入量以及进餐持续时间保持不变,这表明内源性GLP-1是一种较弱的饱腹感信号。然而,血浆PYY和胰高血糖素同时大幅增加可能抵消了ex9-39的促饥饿作用。ex9-39对PYY分泌的影响支持了一种控制L细胞分泌的自抑制反馈机制;对胰岛素和胰高血糖素的影响证实了GLP-1通过对胰腺α和β细胞的作用在血糖控制中的作用。