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Orexin/Hypocretin and MCH Neurons: Cognitive and Motor Roles Beyond Arousal
The lateral hypothalamus (LH) is classically implicated in sleep-wake control. It is the main source of orexin/hypocretin and melanin-concentrating hormone (MCH) neuropeptides in the brain, which have been both implicated in arousal state switching. These neuropeptides are produced by non-overlappin...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8019792/ https://www.ncbi.nlm.nih.gov/pubmed/33828450 http://dx.doi.org/10.3389/fnins.2021.639313 |
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author | Concetti, Cristina Burdakov, Denis |
author_facet | Concetti, Cristina Burdakov, Denis |
author_sort | Concetti, Cristina |
collection | PubMed |
description | The lateral hypothalamus (LH) is classically implicated in sleep-wake control. It is the main source of orexin/hypocretin and melanin-concentrating hormone (MCH) neuropeptides in the brain, which have been both implicated in arousal state switching. These neuropeptides are produced by non-overlapping LH neurons, which both project widely throughout the brain, where release of orexin and MCH activates specific postsynaptic G-protein-coupled receptors. Optogenetic manipulations of orexin and MCH neurons during sleep indicate that they promote awakening and REM sleep, respectively. However, recordings from orexin and MCH neurons in awake, moving animals suggest that they also act outside sleep/wake switching. Here, we review recent studies showing that both orexin and MCH neurons can rapidly (sub-second-timescale) change their firing when awake animals experience external stimuli, or during self-paced exploration of objects and places. However, the sensory-behavioral correlates of orexin and MCH neural activation can be quite different. Orexin neurons are generally more dynamic, with about 2/3rds of them activated before and during self-initiated running, and most activated by sensory stimulation across sensory modalities. MCH neurons are activated in a more select manner, for example upon self-paced investigation of novel objects and by certain other novel stimuli. We discuss optogenetic and chemogenetic manipulations of orexin and MCH neurons, which combined with pharmacological blockade of orexin and MCH receptors, imply that these rapid LH dynamics shape fundamental cognitive and motor processes due to orexin and MCH neuropeptide actions in the awake brain. Finally, we contemplate whether the awake control of psychomotor brain functions by orexin and MCH are distinct from their “arousal” effects. |
format | Online Article Text |
id | pubmed-8019792 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80197922021-04-06 Orexin/Hypocretin and MCH Neurons: Cognitive and Motor Roles Beyond Arousal Concetti, Cristina Burdakov, Denis Front Neurosci Neuroscience The lateral hypothalamus (LH) is classically implicated in sleep-wake control. It is the main source of orexin/hypocretin and melanin-concentrating hormone (MCH) neuropeptides in the brain, which have been both implicated in arousal state switching. These neuropeptides are produced by non-overlapping LH neurons, which both project widely throughout the brain, where release of orexin and MCH activates specific postsynaptic G-protein-coupled receptors. Optogenetic manipulations of orexin and MCH neurons during sleep indicate that they promote awakening and REM sleep, respectively. However, recordings from orexin and MCH neurons in awake, moving animals suggest that they also act outside sleep/wake switching. Here, we review recent studies showing that both orexin and MCH neurons can rapidly (sub-second-timescale) change their firing when awake animals experience external stimuli, or during self-paced exploration of objects and places. However, the sensory-behavioral correlates of orexin and MCH neural activation can be quite different. Orexin neurons are generally more dynamic, with about 2/3rds of them activated before and during self-initiated running, and most activated by sensory stimulation across sensory modalities. MCH neurons are activated in a more select manner, for example upon self-paced investigation of novel objects and by certain other novel stimuli. We discuss optogenetic and chemogenetic manipulations of orexin and MCH neurons, which combined with pharmacological blockade of orexin and MCH receptors, imply that these rapid LH dynamics shape fundamental cognitive and motor processes due to orexin and MCH neuropeptide actions in the awake brain. Finally, we contemplate whether the awake control of psychomotor brain functions by orexin and MCH are distinct from their “arousal” effects. Frontiers Media S.A. 2021-03-22 /pmc/articles/PMC8019792/ /pubmed/33828450 http://dx.doi.org/10.3389/fnins.2021.639313 Text en Copyright © 2021 Concetti and Burdakov. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Concetti, Cristina Burdakov, Denis Orexin/Hypocretin and MCH Neurons: Cognitive and Motor Roles Beyond Arousal |
title | Orexin/Hypocretin and MCH Neurons: Cognitive and Motor Roles Beyond Arousal |
title_full | Orexin/Hypocretin and MCH Neurons: Cognitive and Motor Roles Beyond Arousal |
title_fullStr | Orexin/Hypocretin and MCH Neurons: Cognitive and Motor Roles Beyond Arousal |
title_full_unstemmed | Orexin/Hypocretin and MCH Neurons: Cognitive and Motor Roles Beyond Arousal |
title_short | Orexin/Hypocretin and MCH Neurons: Cognitive and Motor Roles Beyond Arousal |
title_sort | orexin/hypocretin and mch neurons: cognitive and motor roles beyond arousal |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8019792/ https://www.ncbi.nlm.nih.gov/pubmed/33828450 http://dx.doi.org/10.3389/fnins.2021.639313 |
work_keys_str_mv | AT concetticristina orexinhypocretinandmchneuronscognitiveandmotorrolesbeyondarousal AT burdakovdenis orexinhypocretinandmchneuronscognitiveandmotorrolesbeyondarousal |