内分泌学
内科学
葡萄糖稳态
下丘脑
胰高血糖素样肽-1
胰高血糖素
受体
背运动核
弓状核
能量稳态
平衡
化学
人口
生物
胰岛素
迷走神经
医学
糖尿病
胰岛素抵抗
刺激
2型糖尿病
环境卫生
作者
Zhao-Huan Huang,Ling Liu,Jian Zhang,Kristie Conde,Jay Phansalkar,Zhongzhong Li,Lei Yao,Zihui Xu,W. Wang,Jiang‐Ning Zhou,Guo-Qiang Bi,Feng Wu,Randy J. Seeley,Michael M. Scott,Cheng Zhan,Zhiping P. Pang,Ji Liu
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2022-06-10
卷期号:8 (23)
被引量:16
标识
DOI:10.1126/sciadv.abn5345
摘要
Glucagon-like peptide-1 (GLP-1) regulates energy homeostasis via activation of the GLP-1 receptors (GLP-1Rs) in the central nervous system. However, the mechanism by which the central GLP-1 signal controls blood glucose levels, especially in different nutrient states, remains unclear. Here, we defined a population of glucose-sensing GLP-1R neurons in the dorsomedial hypothalamic nucleus (DMH), by which endogenous GLP-1 decreases glucose levels via the cross-talk between the hypothalamus and pancreas. Specifically, we illustrated the sufficiency and necessity of DMH GLP-1R in glucose regulation. The activation of the DMH GLP-1R neurons is mediated by a cAMP-PKA–dependent inhibition of a delayed rectifier potassium current. We also dissected a descending control of DMH GLP-1R –dorsal motor nucleus of the vagus nerve (DMV)–pancreas activity that can regulate glucose levels by increasing insulin release. Thus, our results illustrate how central GLP-1 action in the DMH can induce a nutrient state–dependent reduction in blood glucose level.
科研通智能强力驱动
Strongly Powered by AbleSci AI