内分泌学
内科学
下丘脑
胰高血糖素样肽-1
新陈代谢
碳水化合物代谢
胰高血糖素
受体
化学
血糖调节
生物
胰岛素
医学
糖尿病
2型糖尿病
作者
Zhaohuan Huang,Ling Liu,Jian Zhang,Kristie Conde,Jay Phansalkar,Zhongzhong Li,Lei Yao,Zihui Xu,Wei 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]
日期:2022-06-08
卷期号:8 (23)
被引量:40
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.
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