下丘脑
内科学
内分泌学
食欲
胰高血糖素样肽-1
受体
核心
神经肽
敌手
扁桃形结构
调解人
胰高血糖素
抑制性突触后电位
中枢神经系统
食物摄入量
生物
化学
激素
肽
神经科学
医学
生物化学
2型糖尿病
糖尿病
作者
Mandy D. Turton,Donal O’Shea,I. Gunn,S. A. Beak,C. M. B. Edwards,Karim Meeran,S. J. Choi,Gillian M. Taylor,M. Heath,Philip Lambert,John Wilding,David M. Smith,Mohammad A. Ghatei,J. Herbert,S.R. Bloom
出处
期刊:Nature
[Springer Nature]
日期:1996-01-01
卷期号:379 (6560): 69-72
被引量:1855
摘要
THE sequence of glucagon-like peptide-1 (7–36) amide (GLP-1) is completely conserved in all mammalian species studied, implying that it plays a critical physiological role1. We have shown that GLP-1 and its specific receptors are present in the hypo-thalamus2,3. No physiological role for central GLP-1 has been established. We report here that intracerebroventricular (ICV) GLP-1 powerfully inhibits feeding in fasted rats. ICV injection of the specific GLP-1-receptor antagonist, exendin (9-39)4, blocked the inhibitory effect of GLP-1 on food intake. Exendin (9-39) alone had no influence on fast-induced feeding but more than doubled food intake in satiated rats, and augmented the feeding response to the appetite stimulant, neuropeptide Y. Induction of c-fos is a marker of neuronal activation5. Following ICV GLP-1 injection, c-fos appeared exclusively in the paraventricular nucleus of the hypothalamus and central nucleus of the amygdala, and this was inhibited by prior administration of exendin (9-39). Both of these regions of the brain are of primary importance in the regulation of feeding6. These findings suggest that central GLP-1 is a new physiological mediator of satiety.
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