Glucose-sensing glucagon-like peptide-1 receptor neurons in the dorsomedial hypothalamus regulate glucose metabolism

Author:

Huang Zhaohuan12ORCID,Liu Ling12ORCID,Zhang Jian3ORCID,Conde Kristie45ORCID,Phansalkar Jay45ORCID,Li Zhongzhong1ORCID,Yao Lei3,Xu Zihui45ORCID,Wang Wei6ORCID,Zhou Jiangning3ORCID,Bi Guoqiang23ORCID,Wu Feng12,Seeley Randy J.7ORCID,Scott Michael M.8,Zhan Cheng91011ORCID,Pang Zhiping P.45ORCID,Liu Ji123ORCID

Affiliation:

1. National Engineering Laboratory for Brain-inspired Intelligence Technology and Application, School of Information Science and Technology, University of Science and Technology of China, Anhui, China.

2. Institute of Artificial Intelligence, Hefei Comprehensive National Science Center, Hefei, China.

3. CAS Key Laboratory of Brain Function and Diseases, Life Science School, University of Science and Technology of China, Anhui, China.

4. Child Health Institute of New Jersey, Rutgers University Robert Wood Johnson Medical School, New Brunswick, NJ 08901, USA.

5. Department of Neuroscience and Cell Biology, Rutgers University Robert Wood Johnson Medical School, New Brunswick, NJ 08901, USA.

6. Department of Endocrinology and Laboratory for Diabetes, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Anhui, China,

7. Department of Surgery, University of Michigan, Ann Arbor, MI 48109, USA.

8. Department of Pharmacology, University of Virginia, Charlottesville, VA 22908, USA.

9. Department of Hematology, The First Affiliated Hospital, Life Science School, University of Science and Technology of China, Anhui, China.

10. National Institute of Biological Sciences, Beijing 102206, China.

11. Tsinghua Institute of Multidisciplinary Biomedical Research, Tsinghua University, Beijing 100084, China.

Abstract

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.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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