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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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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. |
format | Online Article Text |
id | pubmed-4844703 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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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