Cargando…
Deciphering an AgRP-serotoninergic neural circuit in distinct control of energy metabolism from feeding
Contrasting to the established role of the hypothalamic agouti-related protein (AgRP) neurons in feeding regulation, the neural circuit and signaling mechanisms by which they control energy expenditure remains unclear. Here, we report that energy expenditure is regulated by a subgroup of AgRP neuron...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8192783/ https://www.ncbi.nlm.nih.gov/pubmed/34112797 http://dx.doi.org/10.1038/s41467-021-23846-x |
_version_ | 1783706109079453696 |
---|---|
author | Han, Yong Xia, Guobin Srisai, Dollada Meng, Fantao He, Yanlin Ran, Yali He, Yang Farias, Monica Hoang, Giang Tóth, István Dietrich, Marcelo O. Chen, Miao-Hsueh Xu, Yong Wu, Qi |
author_facet | Han, Yong Xia, Guobin Srisai, Dollada Meng, Fantao He, Yanlin Ran, Yali He, Yang Farias, Monica Hoang, Giang Tóth, István Dietrich, Marcelo O. Chen, Miao-Hsueh Xu, Yong Wu, Qi |
author_sort | Han, Yong |
collection | PubMed |
description | Contrasting to the established role of the hypothalamic agouti-related protein (AgRP) neurons in feeding regulation, the neural circuit and signaling mechanisms by which they control energy expenditure remains unclear. Here, we report that energy expenditure is regulated by a subgroup of AgRP neurons that send non-collateral projections to neurons within the dorsal lateral part of dorsal raphe nucleus (dlDRN) expressing the melanocortin 4 receptor (MC4R), which in turn innervate nearby serotonergic (5-HT) neurons. Genetic manipulations reveal a bi-directional control of energy expenditure by this circuit without affecting food intake. Fiber photometry and electrophysiological results indicate that the thermo-sensing MC4R(dlDRN) neurons integrate pre-synaptic AgRP signaling, thereby modulating the post-synaptic serotonergic pathway. Specifically, the MC4R(dlDRN) signaling elicits profound, bi-directional, regulation of body weight mainly through sympathetic outflow that reprograms mitochondrial bioenergetics within brown and beige fat while feeding remains intact. Together, we suggest that this AgRP neural circuit plays a unique role in persistent control of energy expenditure and body weight, hinting next-generation therapeutic approaches for obesity and metabolic disorders. |
format | Online Article Text |
id | pubmed-8192783 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81927832021-06-17 Deciphering an AgRP-serotoninergic neural circuit in distinct control of energy metabolism from feeding Han, Yong Xia, Guobin Srisai, Dollada Meng, Fantao He, Yanlin Ran, Yali He, Yang Farias, Monica Hoang, Giang Tóth, István Dietrich, Marcelo O. Chen, Miao-Hsueh Xu, Yong Wu, Qi Nat Commun Article Contrasting to the established role of the hypothalamic agouti-related protein (AgRP) neurons in feeding regulation, the neural circuit and signaling mechanisms by which they control energy expenditure remains unclear. Here, we report that energy expenditure is regulated by a subgroup of AgRP neurons that send non-collateral projections to neurons within the dorsal lateral part of dorsal raphe nucleus (dlDRN) expressing the melanocortin 4 receptor (MC4R), which in turn innervate nearby serotonergic (5-HT) neurons. Genetic manipulations reveal a bi-directional control of energy expenditure by this circuit without affecting food intake. Fiber photometry and electrophysiological results indicate that the thermo-sensing MC4R(dlDRN) neurons integrate pre-synaptic AgRP signaling, thereby modulating the post-synaptic serotonergic pathway. Specifically, the MC4R(dlDRN) signaling elicits profound, bi-directional, regulation of body weight mainly through sympathetic outflow that reprograms mitochondrial bioenergetics within brown and beige fat while feeding remains intact. Together, we suggest that this AgRP neural circuit plays a unique role in persistent control of energy expenditure and body weight, hinting next-generation therapeutic approaches for obesity and metabolic disorders. Nature Publishing Group UK 2021-06-10 /pmc/articles/PMC8192783/ /pubmed/34112797 http://dx.doi.org/10.1038/s41467-021-23846-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Han, Yong Xia, Guobin Srisai, Dollada Meng, Fantao He, Yanlin Ran, Yali He, Yang Farias, Monica Hoang, Giang Tóth, István Dietrich, Marcelo O. Chen, Miao-Hsueh Xu, Yong Wu, Qi Deciphering an AgRP-serotoninergic neural circuit in distinct control of energy metabolism from feeding |
title | Deciphering an AgRP-serotoninergic neural circuit in distinct control of energy metabolism from feeding |
title_full | Deciphering an AgRP-serotoninergic neural circuit in distinct control of energy metabolism from feeding |
title_fullStr | Deciphering an AgRP-serotoninergic neural circuit in distinct control of energy metabolism from feeding |
title_full_unstemmed | Deciphering an AgRP-serotoninergic neural circuit in distinct control of energy metabolism from feeding |
title_short | Deciphering an AgRP-serotoninergic neural circuit in distinct control of energy metabolism from feeding |
title_sort | deciphering an agrp-serotoninergic neural circuit in distinct control of energy metabolism from feeding |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8192783/ https://www.ncbi.nlm.nih.gov/pubmed/34112797 http://dx.doi.org/10.1038/s41467-021-23846-x |
work_keys_str_mv | AT hanyong decipheringanagrpserotoninergicneuralcircuitindistinctcontrolofenergymetabolismfromfeeding AT xiaguobin decipheringanagrpserotoninergicneuralcircuitindistinctcontrolofenergymetabolismfromfeeding AT srisaidollada decipheringanagrpserotoninergicneuralcircuitindistinctcontrolofenergymetabolismfromfeeding AT mengfantao decipheringanagrpserotoninergicneuralcircuitindistinctcontrolofenergymetabolismfromfeeding AT heyanlin decipheringanagrpserotoninergicneuralcircuitindistinctcontrolofenergymetabolismfromfeeding AT ranyali decipheringanagrpserotoninergicneuralcircuitindistinctcontrolofenergymetabolismfromfeeding AT heyang decipheringanagrpserotoninergicneuralcircuitindistinctcontrolofenergymetabolismfromfeeding AT fariasmonica decipheringanagrpserotoninergicneuralcircuitindistinctcontrolofenergymetabolismfromfeeding AT hoanggiang decipheringanagrpserotoninergicneuralcircuitindistinctcontrolofenergymetabolismfromfeeding AT tothistvan decipheringanagrpserotoninergicneuralcircuitindistinctcontrolofenergymetabolismfromfeeding AT dietrichmarceloo decipheringanagrpserotoninergicneuralcircuitindistinctcontrolofenergymetabolismfromfeeding AT chenmiaohsueh decipheringanagrpserotoninergicneuralcircuitindistinctcontrolofenergymetabolismfromfeeding AT xuyong decipheringanagrpserotoninergicneuralcircuitindistinctcontrolofenergymetabolismfromfeeding AT wuqi decipheringanagrpserotoninergicneuralcircuitindistinctcontrolofenergymetabolismfromfeeding |