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Awake dynamics and brain-wide direct inputs of hypothalamic MCH and orexin networks

The lateral hypothalamus (LH) controls energy balance. LH melanin-concentrating-hormone (MCH) and orexin/hypocretin (OH) neurons mediate energy accumulation and expenditure, respectively. MCH cells promote memory and appropriate stimulus-reward associations; their inactivation disrupts energy-optima...

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Autores principales: González, J. Antonio, Iordanidou, Panagiota, Strom, Molly, Adamantidis, Antoine, Burdakov, Denis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4844703/
https://www.ncbi.nlm.nih.gov/pubmed/27102565
http://dx.doi.org/10.1038/ncomms11395
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author González, J. Antonio
Iordanidou, Panagiota
Strom, Molly
Adamantidis, Antoine
Burdakov, Denis
author_facet González, J. Antonio
Iordanidou, Panagiota
Strom, Molly
Adamantidis, Antoine
Burdakov, Denis
author_sort González, J. Antonio
collection PubMed
description The lateral hypothalamus (LH) controls energy balance. LH melanin-concentrating-hormone (MCH) and orexin/hypocretin (OH) neurons mediate energy accumulation and expenditure, respectively. MCH cells promote memory and appropriate stimulus-reward associations; their inactivation disrupts energy-optimal behaviour and causes weight loss. However, MCH cell dynamics during wakefulness are unknown, leaving it unclear if they differentially participate in brain activity during sensory processing. By fiberoptic recordings from molecularly defined populations of LH neurons in awake freely moving mice, we show that MCH neurons generate conditional population bursts. This MCH cell activity correlates with novelty exploration, is inhibited by stress and is inversely predicted by OH cell activity. Furthermore, we obtain brain-wide maps of monosynaptic inputs to MCH and OH cells, and demonstrate optogenetically that VGAT neurons in the amygdala and bed nucleus of stria terminalis inhibit MCH cells. These data reveal cell-type-specific LH dynamics during sensory integration, and identify direct neural controllers of MCH neurons.
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spelling pubmed-48447032016-04-27 Awake dynamics and brain-wide direct inputs of hypothalamic MCH and orexin networks González, J. Antonio Iordanidou, Panagiota Strom, Molly Adamantidis, Antoine Burdakov, Denis Nat Commun Article The lateral hypothalamus (LH) controls energy balance. LH melanin-concentrating-hormone (MCH) and orexin/hypocretin (OH) neurons mediate energy accumulation and expenditure, respectively. MCH cells promote memory and appropriate stimulus-reward associations; their inactivation disrupts energy-optimal behaviour and causes weight loss. However, MCH cell dynamics during wakefulness are unknown, leaving it unclear if they differentially participate in brain activity during sensory processing. By fiberoptic recordings from molecularly defined populations of LH neurons in awake freely moving mice, we show that MCH neurons generate conditional population bursts. This MCH cell activity correlates with novelty exploration, is inhibited by stress and is inversely predicted by OH cell activity. Furthermore, we obtain brain-wide maps of monosynaptic inputs to MCH and OH cells, and demonstrate optogenetically that VGAT neurons in the amygdala and bed nucleus of stria terminalis inhibit MCH cells. These data reveal cell-type-specific LH dynamics during sensory integration, and identify direct neural controllers of MCH neurons. Nature Publishing Group 2016-04-22 /pmc/articles/PMC4844703/ /pubmed/27102565 http://dx.doi.org/10.1038/ncomms11395 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
González, J. Antonio
Iordanidou, Panagiota
Strom, Molly
Adamantidis, Antoine
Burdakov, Denis
Awake dynamics and brain-wide direct inputs of hypothalamic MCH and orexin networks
title Awake dynamics and brain-wide direct inputs of hypothalamic MCH and orexin networks
title_full Awake dynamics and brain-wide direct inputs of hypothalamic MCH and orexin networks
title_fullStr Awake dynamics and brain-wide direct inputs of hypothalamic MCH and orexin networks
title_full_unstemmed Awake dynamics and brain-wide direct inputs of hypothalamic MCH and orexin networks
title_short Awake dynamics and brain-wide direct inputs of hypothalamic MCH and orexin networks
title_sort awake dynamics and brain-wide direct inputs of hypothalamic mch and orexin networks
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4844703/
https://www.ncbi.nlm.nih.gov/pubmed/27102565
http://dx.doi.org/10.1038/ncomms11395
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