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UP-DOWN cortical dynamics reflect state transitions in a bistable network

In the idling brain, neuronal circuits transition between periods of sustained firing (UP state) and quiescence (DOWN state), a pattern the mechanisms of which remain unclear. Here we analyzed spontaneous cortical population activity from anesthetized rats and found that UP and DOWN durations were h...

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Autores principales: Jercog, Daniel, Roxin, Alex, Barthó, Peter, Luczak, Artur, Compte, Albert, de la Rocha, Jaime
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5582872/
https://www.ncbi.nlm.nih.gov/pubmed/28826485
http://dx.doi.org/10.7554/eLife.22425
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author Jercog, Daniel
Roxin, Alex
Barthó, Peter
Luczak, Artur
Compte, Albert
de la Rocha, Jaime
author_facet Jercog, Daniel
Roxin, Alex
Barthó, Peter
Luczak, Artur
Compte, Albert
de la Rocha, Jaime
author_sort Jercog, Daniel
collection PubMed
description In the idling brain, neuronal circuits transition between periods of sustained firing (UP state) and quiescence (DOWN state), a pattern the mechanisms of which remain unclear. Here we analyzed spontaneous cortical population activity from anesthetized rats and found that UP and DOWN durations were highly variable and that population rates showed no significant decay during UP periods. We built a network rate model with excitatory (E) and inhibitory (I) populations exhibiting a novel bistable regime between a quiescent and an inhibition-stabilized state of arbitrarily low rate. Fluctuations triggered state transitions, while adaptation in E cells paradoxically caused a marginal decay of E-rate but a marked decay of I-rate in UP periods, a prediction that we validated experimentally. A spiking network implementation further predicted that DOWN-to-UP transitions must be caused by synchronous high-amplitude events. Our findings provide evidence of bistable cortical networks that exhibit non-rhythmic state transitions when the brain rests.
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spelling pubmed-55828722017-09-06 UP-DOWN cortical dynamics reflect state transitions in a bistable network Jercog, Daniel Roxin, Alex Barthó, Peter Luczak, Artur Compte, Albert de la Rocha, Jaime eLife Neuroscience In the idling brain, neuronal circuits transition between periods of sustained firing (UP state) and quiescence (DOWN state), a pattern the mechanisms of which remain unclear. Here we analyzed spontaneous cortical population activity from anesthetized rats and found that UP and DOWN durations were highly variable and that population rates showed no significant decay during UP periods. We built a network rate model with excitatory (E) and inhibitory (I) populations exhibiting a novel bistable regime between a quiescent and an inhibition-stabilized state of arbitrarily low rate. Fluctuations triggered state transitions, while adaptation in E cells paradoxically caused a marginal decay of E-rate but a marked decay of I-rate in UP periods, a prediction that we validated experimentally. A spiking network implementation further predicted that DOWN-to-UP transitions must be caused by synchronous high-amplitude events. Our findings provide evidence of bistable cortical networks that exhibit non-rhythmic state transitions when the brain rests. eLife Sciences Publications, Ltd 2017-08-04 /pmc/articles/PMC5582872/ /pubmed/28826485 http://dx.doi.org/10.7554/eLife.22425 Text en © 2017, Jercog et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Jercog, Daniel
Roxin, Alex
Barthó, Peter
Luczak, Artur
Compte, Albert
de la Rocha, Jaime
UP-DOWN cortical dynamics reflect state transitions in a bistable network
title UP-DOWN cortical dynamics reflect state transitions in a bistable network
title_full UP-DOWN cortical dynamics reflect state transitions in a bistable network
title_fullStr UP-DOWN cortical dynamics reflect state transitions in a bistable network
title_full_unstemmed UP-DOWN cortical dynamics reflect state transitions in a bistable network
title_short UP-DOWN cortical dynamics reflect state transitions in a bistable network
title_sort up-down cortical dynamics reflect state transitions in a bistable network
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5582872/
https://www.ncbi.nlm.nih.gov/pubmed/28826485
http://dx.doi.org/10.7554/eLife.22425
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