Cargando…
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...
Autores principales: | , , , , , |
---|---|
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 |
_version_ | 1783261253958893568 |
---|---|
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. |
format | Online Article Text |
id | pubmed-5582872 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT jercogdaniel updowncorticaldynamicsreflectstatetransitionsinabistablenetwork AT roxinalex updowncorticaldynamicsreflectstatetransitionsinabistablenetwork AT barthopeter updowncorticaldynamicsreflectstatetransitionsinabistablenetwork AT luczakartur updowncorticaldynamicsreflectstatetransitionsinabistablenetwork AT comptealbert updowncorticaldynamicsreflectstatetransitionsinabistablenetwork AT delarochajaime updowncorticaldynamicsreflectstatetransitionsinabistablenetwork |