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Ongoing Network State Controls the Length of Sleep Spindles via Inhibitory Activity
Sleep spindles are major transient oscillations of the mammalian brain. Spindles are generated in the thalamus; however, what determines their duration is presently unclear. Here, we measured somatic activity of excitatory thalamocortical (TC) cells together with axonal activity of reciprocally coup...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4064116/ https://www.ncbi.nlm.nih.gov/pubmed/24945776 http://dx.doi.org/10.1016/j.neuron.2014.04.046 |
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author | Barthó, Péter Slézia, Andrea Mátyás, Ferenc Faradzs-Zade, Lejla Ulbert, István Harris, Kenneth D. Acsády, László |
author_facet | Barthó, Péter Slézia, Andrea Mátyás, Ferenc Faradzs-Zade, Lejla Ulbert, István Harris, Kenneth D. Acsády, László |
author_sort | Barthó, Péter |
collection | PubMed |
description | Sleep spindles are major transient oscillations of the mammalian brain. Spindles are generated in the thalamus; however, what determines their duration is presently unclear. Here, we measured somatic activity of excitatory thalamocortical (TC) cells together with axonal activity of reciprocally coupled inhibitory reticular thalamic cells (nRTs) and quantified cycle-by-cycle alterations in their firing in vivo. We found that spindles with different durations were paralleled by distinct nRT activity, and nRT firing sharply dropped before the termination of all spindles. Both initial nRT and TC activity was correlated with spindle length, but nRT correlation was more robust. Analysis of spindles evoked by optogenetic activation of nRT showed that spindle probability, but not spindle length, was determined by the strength of the light stimulus. Our data indicate that during natural sleep a dynamically fluctuating thalamocortical network controls the duration of sleep spindles via the major inhibitory element of the circuits, the nRT. |
format | Online Article Text |
id | pubmed-4064116 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-40641162014-06-20 Ongoing Network State Controls the Length of Sleep Spindles via Inhibitory Activity Barthó, Péter Slézia, Andrea Mátyás, Ferenc Faradzs-Zade, Lejla Ulbert, István Harris, Kenneth D. Acsády, László Neuron Article Sleep spindles are major transient oscillations of the mammalian brain. Spindles are generated in the thalamus; however, what determines their duration is presently unclear. Here, we measured somatic activity of excitatory thalamocortical (TC) cells together with axonal activity of reciprocally coupled inhibitory reticular thalamic cells (nRTs) and quantified cycle-by-cycle alterations in their firing in vivo. We found that spindles with different durations were paralleled by distinct nRT activity, and nRT firing sharply dropped before the termination of all spindles. Both initial nRT and TC activity was correlated with spindle length, but nRT correlation was more robust. Analysis of spindles evoked by optogenetic activation of nRT showed that spindle probability, but not spindle length, was determined by the strength of the light stimulus. Our data indicate that during natural sleep a dynamically fluctuating thalamocortical network controls the duration of sleep spindles via the major inhibitory element of the circuits, the nRT. Cell Press 2014-06-18 /pmc/articles/PMC4064116/ /pubmed/24945776 http://dx.doi.org/10.1016/j.neuron.2014.04.046 Text en © 2014 The Authors http://creativecommons.org/licenses/by/3.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Barthó, Péter Slézia, Andrea Mátyás, Ferenc Faradzs-Zade, Lejla Ulbert, István Harris, Kenneth D. Acsády, László Ongoing Network State Controls the Length of Sleep Spindles via Inhibitory Activity |
title | Ongoing Network State Controls the Length of Sleep Spindles via Inhibitory Activity |
title_full | Ongoing Network State Controls the Length of Sleep Spindles via Inhibitory Activity |
title_fullStr | Ongoing Network State Controls the Length of Sleep Spindles via Inhibitory Activity |
title_full_unstemmed | Ongoing Network State Controls the Length of Sleep Spindles via Inhibitory Activity |
title_short | Ongoing Network State Controls the Length of Sleep Spindles via Inhibitory Activity |
title_sort | ongoing network state controls the length of sleep spindles via inhibitory activity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4064116/ https://www.ncbi.nlm.nih.gov/pubmed/24945776 http://dx.doi.org/10.1016/j.neuron.2014.04.046 |
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