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Arousal State-Dependent Alterations in Neural Activity in the Zebra Finch VTA/SNc

Sleep-wake behaviors are important for survival and highly conserved among animal species. A growing body of evidence indicates that the midbrain dopaminergic system is associated with sleep-wake regulation in mammals. Songbirds exhibit mammalian-like sleep structures, and neurons in the midbrain ve...

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Autores principales: Yanagihara, Shin, Ikebuchi, Maki, Mori, Chihiro, Tachibana, Ryosuke O., Okanoya, Kazuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7472990/
https://www.ncbi.nlm.nih.gov/pubmed/32973441
http://dx.doi.org/10.3389/fnins.2020.00897
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author Yanagihara, Shin
Ikebuchi, Maki
Mori, Chihiro
Tachibana, Ryosuke O.
Okanoya, Kazuo
author_facet Yanagihara, Shin
Ikebuchi, Maki
Mori, Chihiro
Tachibana, Ryosuke O.
Okanoya, Kazuo
author_sort Yanagihara, Shin
collection PubMed
description Sleep-wake behaviors are important for survival and highly conserved among animal species. A growing body of evidence indicates that the midbrain dopaminergic system is associated with sleep-wake regulation in mammals. Songbirds exhibit mammalian-like sleep structures, and neurons in the midbrain ventral tegmental area (VTA) and substantia nigra pars compacta (SNc) possess physiological properties similar to those in mammals. However, it remains uncertain whether the neurons in the songbird VTA/SNc are associated with sleep-wake regulation. Here, we show that VTA/SNc neurons in zebra finches exhibit arousal state-dependent alterations in spontaneous neural activity. By recording extracellular single-unit activity from anesthetized or freely behaving zebra finches, we found that VTA/SNc neurons exhibited increased firing rates during wakefulness, and the same population of neurons displayed reduced firing rates during anesthesia and slow-wave sleep. These results suggest that the songbird VTA/SNc is associated with the regulation of sleep and wakefulness along with other arousal regulatory systems. These findings raise the possibility that fundamental neural mechanisms of sleep-wake behaviors are evolutionarily conserved between birds and mammals.
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spelling pubmed-74729902020-09-23 Arousal State-Dependent Alterations in Neural Activity in the Zebra Finch VTA/SNc Yanagihara, Shin Ikebuchi, Maki Mori, Chihiro Tachibana, Ryosuke O. Okanoya, Kazuo Front Neurosci Neuroscience Sleep-wake behaviors are important for survival and highly conserved among animal species. A growing body of evidence indicates that the midbrain dopaminergic system is associated with sleep-wake regulation in mammals. Songbirds exhibit mammalian-like sleep structures, and neurons in the midbrain ventral tegmental area (VTA) and substantia nigra pars compacta (SNc) possess physiological properties similar to those in mammals. However, it remains uncertain whether the neurons in the songbird VTA/SNc are associated with sleep-wake regulation. Here, we show that VTA/SNc neurons in zebra finches exhibit arousal state-dependent alterations in spontaneous neural activity. By recording extracellular single-unit activity from anesthetized or freely behaving zebra finches, we found that VTA/SNc neurons exhibited increased firing rates during wakefulness, and the same population of neurons displayed reduced firing rates during anesthesia and slow-wave sleep. These results suggest that the songbird VTA/SNc is associated with the regulation of sleep and wakefulness along with other arousal regulatory systems. These findings raise the possibility that fundamental neural mechanisms of sleep-wake behaviors are evolutionarily conserved between birds and mammals. Frontiers Media S.A. 2020-08-21 /pmc/articles/PMC7472990/ /pubmed/32973441 http://dx.doi.org/10.3389/fnins.2020.00897 Text en Copyright © 2020 Yanagihara, Ikebuchi, Mori, Tachibana and Okanoya. 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
Yanagihara, Shin
Ikebuchi, Maki
Mori, Chihiro
Tachibana, Ryosuke O.
Okanoya, Kazuo
Arousal State-Dependent Alterations in Neural Activity in the Zebra Finch VTA/SNc
title Arousal State-Dependent Alterations in Neural Activity in the Zebra Finch VTA/SNc
title_full Arousal State-Dependent Alterations in Neural Activity in the Zebra Finch VTA/SNc
title_fullStr Arousal State-Dependent Alterations in Neural Activity in the Zebra Finch VTA/SNc
title_full_unstemmed Arousal State-Dependent Alterations in Neural Activity in the Zebra Finch VTA/SNc
title_short Arousal State-Dependent Alterations in Neural Activity in the Zebra Finch VTA/SNc
title_sort arousal state-dependent alterations in neural activity in the zebra finch vta/snc
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7472990/
https://www.ncbi.nlm.nih.gov/pubmed/32973441
http://dx.doi.org/10.3389/fnins.2020.00897
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