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Role of spontaneous and sensory orexin network dynamics in rapid locomotion initiation
Appropriate motor control is critical for normal life, and requires hypothalamic hypocretin/orexin neurons (HONs). HONs are slowly regulated by nutrients, but also display rapid (subsecond) activity fluctuations in vivo. The necessity of these activity bursts for sensorimotor control and their roles...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Pergamon Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7086232/ https://www.ncbi.nlm.nih.gov/pubmed/32058043 http://dx.doi.org/10.1016/j.pneurobio.2020.101771 |
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author | Karnani, Mahesh M. Schöne, Cornelia Bracey, Edward F. González, J. Antonio Viskaitis, Paulius Li, Han-Tao Adamantidis, Antoine Burdakov, Denis |
author_facet | Karnani, Mahesh M. Schöne, Cornelia Bracey, Edward F. González, J. Antonio Viskaitis, Paulius Li, Han-Tao Adamantidis, Antoine Burdakov, Denis |
author_sort | Karnani, Mahesh M. |
collection | PubMed |
description | Appropriate motor control is critical for normal life, and requires hypothalamic hypocretin/orexin neurons (HONs). HONs are slowly regulated by nutrients, but also display rapid (subsecond) activity fluctuations in vivo. The necessity of these activity bursts for sensorimotor control and their roles in specific phases of movement are unknown. Here we show that temporally-restricted optosilencing of spontaneous or sensory-evoked HON bursts disrupts locomotion initiation, but does not affect ongoing locomotion. Conversely, HON optostimulation initiates locomotion with subsecond delays in a frequency-dependent manner. Using 2-photon volumetric imaging of activity of >300 HONs during sensory stimulation and self-initiated locomotion, we identify several locomotion-related HON subtypes, which distinctly predict the probability of imminent locomotion initiation, display distinct sensory responses, and are differentially modulated by food deprivation. By causally linking HON bursts to locomotion initiation, these findings reveal the sensorimotor importance of rapid spontaneous and evoked fluctuations in HON ensemble activity. |
format | Online Article Text |
id | pubmed-7086232 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Pergamon Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-70862322020-04-01 Role of spontaneous and sensory orexin network dynamics in rapid locomotion initiation Karnani, Mahesh M. Schöne, Cornelia Bracey, Edward F. González, J. Antonio Viskaitis, Paulius Li, Han-Tao Adamantidis, Antoine Burdakov, Denis Prog Neurobiol Article Appropriate motor control is critical for normal life, and requires hypothalamic hypocretin/orexin neurons (HONs). HONs are slowly regulated by nutrients, but also display rapid (subsecond) activity fluctuations in vivo. The necessity of these activity bursts for sensorimotor control and their roles in specific phases of movement are unknown. Here we show that temporally-restricted optosilencing of spontaneous or sensory-evoked HON bursts disrupts locomotion initiation, but does not affect ongoing locomotion. Conversely, HON optostimulation initiates locomotion with subsecond delays in a frequency-dependent manner. Using 2-photon volumetric imaging of activity of >300 HONs during sensory stimulation and self-initiated locomotion, we identify several locomotion-related HON subtypes, which distinctly predict the probability of imminent locomotion initiation, display distinct sensory responses, and are differentially modulated by food deprivation. By causally linking HON bursts to locomotion initiation, these findings reveal the sensorimotor importance of rapid spontaneous and evoked fluctuations in HON ensemble activity. Pergamon Press 2020-04 /pmc/articles/PMC7086232/ /pubmed/32058043 http://dx.doi.org/10.1016/j.pneurobio.2020.101771 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Karnani, Mahesh M. Schöne, Cornelia Bracey, Edward F. González, J. Antonio Viskaitis, Paulius Li, Han-Tao Adamantidis, Antoine Burdakov, Denis Role of spontaneous and sensory orexin network dynamics in rapid locomotion initiation |
title | Role of spontaneous and sensory orexin network dynamics in rapid locomotion initiation |
title_full | Role of spontaneous and sensory orexin network dynamics in rapid locomotion initiation |
title_fullStr | Role of spontaneous and sensory orexin network dynamics in rapid locomotion initiation |
title_full_unstemmed | Role of spontaneous and sensory orexin network dynamics in rapid locomotion initiation |
title_short | Role of spontaneous and sensory orexin network dynamics in rapid locomotion initiation |
title_sort | role of spontaneous and sensory orexin network dynamics in rapid locomotion initiation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7086232/ https://www.ncbi.nlm.nih.gov/pubmed/32058043 http://dx.doi.org/10.1016/j.pneurobio.2020.101771 |
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