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Parallel Arousal Pathways in the Lateral Hypothalamus

Until recently, hypocretin (Hcrt) neurons were the only known wake-promoting neuronal population in the lateral hypothalamus (LH), but subpopulations of inhibitory neurons in this area and glutamatergic neurons in the nearby supramammillary nucleus (SuM) have recently been found that also promote wa...

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Autores principales: Heiss, Jaime E., Yamanaka, Akihiro, Kilduff, Thomas S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6140123/
https://www.ncbi.nlm.nih.gov/pubmed/30225361
http://dx.doi.org/10.1523/ENEURO.0228-18.2018
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author Heiss, Jaime E.
Yamanaka, Akihiro
Kilduff, Thomas S.
author_facet Heiss, Jaime E.
Yamanaka, Akihiro
Kilduff, Thomas S.
author_sort Heiss, Jaime E.
collection PubMed
description Until recently, hypocretin (Hcrt) neurons were the only known wake-promoting neuronal population in the lateral hypothalamus (LH), but subpopulations of inhibitory neurons in this area and glutamatergic neurons in the nearby supramammillary nucleus (SuM) have recently been found that also promote wakefulness. We performed chemogenetic excitation of LH neurons in mice and observed increased wakefulness that lasted more than 4 h without unusual behavior or EEG anomalies. The increased wakefulness was similar in the presence or absence of the dual orexin receptor blocker almorexant (ALM). Analysis of hM3Dq transfection and c-FOS expression in LH inhibitory neurons and in the SuM failed to confirm that the increased wakefulness was due to these wake-promoting populations, although this possibility cannot be completely excluded. To evaluate the relationship to the Hcrt system, we repeated the study in Orexin-tTA mice in the presence or absence of dietary doxycycline (DOX), which enabled us to manipulate the percentage of Hcrt neurons that expressed hM3Dq. In DOX-fed mice, 18% of Hcrt neurons as well as many other LH neurons expressed hM3Dq; these mice showed a profound increase in wake after hM3Dq activation even in the presence of ALM. In mice switched to normal chow, 62% of Hcrt neurons expressed hM3Dq along with other LH cells; chemogenetic activation produced even more sustained arousal which could be reduced to previous levels by ALM treatment. Together, these results indicate an LH neuron population that promotes wakefulness through an Hcrt-independent pathway that can act synergistically with the Hcrt system to prolong arousal.
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spelling pubmed-61401232018-09-17 Parallel Arousal Pathways in the Lateral Hypothalamus Heiss, Jaime E. Yamanaka, Akihiro Kilduff, Thomas S. eNeuro New Research Until recently, hypocretin (Hcrt) neurons were the only known wake-promoting neuronal population in the lateral hypothalamus (LH), but subpopulations of inhibitory neurons in this area and glutamatergic neurons in the nearby supramammillary nucleus (SuM) have recently been found that also promote wakefulness. We performed chemogenetic excitation of LH neurons in mice and observed increased wakefulness that lasted more than 4 h without unusual behavior or EEG anomalies. The increased wakefulness was similar in the presence or absence of the dual orexin receptor blocker almorexant (ALM). Analysis of hM3Dq transfection and c-FOS expression in LH inhibitory neurons and in the SuM failed to confirm that the increased wakefulness was due to these wake-promoting populations, although this possibility cannot be completely excluded. To evaluate the relationship to the Hcrt system, we repeated the study in Orexin-tTA mice in the presence or absence of dietary doxycycline (DOX), which enabled us to manipulate the percentage of Hcrt neurons that expressed hM3Dq. In DOX-fed mice, 18% of Hcrt neurons as well as many other LH neurons expressed hM3Dq; these mice showed a profound increase in wake after hM3Dq activation even in the presence of ALM. In mice switched to normal chow, 62% of Hcrt neurons expressed hM3Dq along with other LH cells; chemogenetic activation produced even more sustained arousal which could be reduced to previous levels by ALM treatment. Together, these results indicate an LH neuron population that promotes wakefulness through an Hcrt-independent pathway that can act synergistically with the Hcrt system to prolong arousal. Society for Neuroscience 2018-08-21 /pmc/articles/PMC6140123/ /pubmed/30225361 http://dx.doi.org/10.1523/ENEURO.0228-18.2018 Text en Copyright © 2018 Heiss et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle New Research
Heiss, Jaime E.
Yamanaka, Akihiro
Kilduff, Thomas S.
Parallel Arousal Pathways in the Lateral Hypothalamus
title Parallel Arousal Pathways in the Lateral Hypothalamus
title_full Parallel Arousal Pathways in the Lateral Hypothalamus
title_fullStr Parallel Arousal Pathways in the Lateral Hypothalamus
title_full_unstemmed Parallel Arousal Pathways in the Lateral Hypothalamus
title_short Parallel Arousal Pathways in the Lateral Hypothalamus
title_sort parallel arousal pathways in the lateral hypothalamus
topic New Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6140123/
https://www.ncbi.nlm.nih.gov/pubmed/30225361
http://dx.doi.org/10.1523/ENEURO.0228-18.2018
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