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Circadian and Homeostatic Modulation of Multi-Unit Activity in Midbrain Dopaminergic Structures
Although the link between sleep disturbances and dopamine (DA)-related neurological and neuropsychiatric disorders is well established, the impact of sleep alterations on neuronal activity of midbrain DA-ergic structures is currently unknown. Here, using wildtype C57Bl mice, we investigated the circ...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5958140/ https://www.ncbi.nlm.nih.gov/pubmed/29773830 http://dx.doi.org/10.1038/s41598-018-25770-5 |
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author | Fifel, Karim Meijer, Johanna H. Deboer, Tom |
author_facet | Fifel, Karim Meijer, Johanna H. Deboer, Tom |
author_sort | Fifel, Karim |
collection | PubMed |
description | Although the link between sleep disturbances and dopamine (DA)-related neurological and neuropsychiatric disorders is well established, the impact of sleep alterations on neuronal activity of midbrain DA-ergic structures is currently unknown. Here, using wildtype C57Bl mice, we investigated the circadian- and sleep-related modulation of electrical neuronal activity in midbrain ventral-tegmental-area (VTA) and substantia nigra (SN). We found no significant circadian modulation of activity in SN while VTA displayed a low amplitude but significant circadian modulation with increased firing rates during the active phase. Combining neural activity recordings with electroencephalogram (EEG) recordings revealed a strong vigilance state dependent modulation of neuronal activity with increased activity during wakefulness and rapid eye movement sleep relative to non-rapid eye movement sleep in both SN and VTA. Six-hours of sleep deprivation induced a significant depression of neuronal activity in both areas. Surprisingly, these alterations lasted for up to 48 hours and persisted even after the normalization of cortical EEG waves. Our results show that sleep and sleep disturbances significantly affect neuronal activity in midbrain DA structures. We propose that these changes in neuronal activity underlie the well-known relationship between sleep alterations and several disorders involving dysfunction of the DA circuitry such as addiction and depression. |
format | Online Article Text |
id | pubmed-5958140 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59581402018-05-24 Circadian and Homeostatic Modulation of Multi-Unit Activity in Midbrain Dopaminergic Structures Fifel, Karim Meijer, Johanna H. Deboer, Tom Sci Rep Article Although the link between sleep disturbances and dopamine (DA)-related neurological and neuropsychiatric disorders is well established, the impact of sleep alterations on neuronal activity of midbrain DA-ergic structures is currently unknown. Here, using wildtype C57Bl mice, we investigated the circadian- and sleep-related modulation of electrical neuronal activity in midbrain ventral-tegmental-area (VTA) and substantia nigra (SN). We found no significant circadian modulation of activity in SN while VTA displayed a low amplitude but significant circadian modulation with increased firing rates during the active phase. Combining neural activity recordings with electroencephalogram (EEG) recordings revealed a strong vigilance state dependent modulation of neuronal activity with increased activity during wakefulness and rapid eye movement sleep relative to non-rapid eye movement sleep in both SN and VTA. Six-hours of sleep deprivation induced a significant depression of neuronal activity in both areas. Surprisingly, these alterations lasted for up to 48 hours and persisted even after the normalization of cortical EEG waves. Our results show that sleep and sleep disturbances significantly affect neuronal activity in midbrain DA structures. We propose that these changes in neuronal activity underlie the well-known relationship between sleep alterations and several disorders involving dysfunction of the DA circuitry such as addiction and depression. Nature Publishing Group UK 2018-05-17 /pmc/articles/PMC5958140/ /pubmed/29773830 http://dx.doi.org/10.1038/s41598-018-25770-5 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Fifel, Karim Meijer, Johanna H. Deboer, Tom Circadian and Homeostatic Modulation of Multi-Unit Activity in Midbrain Dopaminergic Structures |
title | Circadian and Homeostatic Modulation of Multi-Unit Activity in Midbrain Dopaminergic Structures |
title_full | Circadian and Homeostatic Modulation of Multi-Unit Activity in Midbrain Dopaminergic Structures |
title_fullStr | Circadian and Homeostatic Modulation of Multi-Unit Activity in Midbrain Dopaminergic Structures |
title_full_unstemmed | Circadian and Homeostatic Modulation of Multi-Unit Activity in Midbrain Dopaminergic Structures |
title_short | Circadian and Homeostatic Modulation of Multi-Unit Activity in Midbrain Dopaminergic Structures |
title_sort | circadian and homeostatic modulation of multi-unit activity in midbrain dopaminergic structures |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5958140/ https://www.ncbi.nlm.nih.gov/pubmed/29773830 http://dx.doi.org/10.1038/s41598-018-25770-5 |
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