Cargando…
Broadband macroscopic cortical oscillations emerge from intrinsic neuronal response failures
Broadband spontaneous macroscopic neural oscillations are rhythmic cortical firing which were extensively examined during the last century, however, their possible origination is still controversial. In this work we show how macroscopic oscillations emerge in solely excitatory random networks and wi...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4626558/ https://www.ncbi.nlm.nih.gov/pubmed/26578893 http://dx.doi.org/10.3389/fncir.2015.00065 |
_version_ | 1782398123087233024 |
---|---|
author | Goldental, Amir Vardi, Roni Sardi, Shira Sabo, Pinhas Kanter, Ido |
author_facet | Goldental, Amir Vardi, Roni Sardi, Shira Sabo, Pinhas Kanter, Ido |
author_sort | Goldental, Amir |
collection | PubMed |
description | Broadband spontaneous macroscopic neural oscillations are rhythmic cortical firing which were extensively examined during the last century, however, their possible origination is still controversial. In this work we show how macroscopic oscillations emerge in solely excitatory random networks and without topological constraints. We experimentally and theoretically show that these oscillations stem from the counterintuitive underlying mechanism—the intrinsic stochastic neuronal response failures (NRFs). These NRFs, which are characterized by short-term memory, lead to cooperation among neurons, resulting in sub- or several- Hertz macroscopic oscillations which coexist with high frequency gamma oscillations. A quantitative interplay between the statistical network properties and the emerging oscillations is supported by simulations of large networks based on single-neuron in-vitro experiments and a Langevin equation describing the network dynamics. Results call for the examination of these oscillations in the presence of inhibition and external drives. |
format | Online Article Text |
id | pubmed-4626558 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-46265582015-11-17 Broadband macroscopic cortical oscillations emerge from intrinsic neuronal response failures Goldental, Amir Vardi, Roni Sardi, Shira Sabo, Pinhas Kanter, Ido Front Neural Circuits Neuroscience Broadband spontaneous macroscopic neural oscillations are rhythmic cortical firing which were extensively examined during the last century, however, their possible origination is still controversial. In this work we show how macroscopic oscillations emerge in solely excitatory random networks and without topological constraints. We experimentally and theoretically show that these oscillations stem from the counterintuitive underlying mechanism—the intrinsic stochastic neuronal response failures (NRFs). These NRFs, which are characterized by short-term memory, lead to cooperation among neurons, resulting in sub- or several- Hertz macroscopic oscillations which coexist with high frequency gamma oscillations. A quantitative interplay between the statistical network properties and the emerging oscillations is supported by simulations of large networks based on single-neuron in-vitro experiments and a Langevin equation describing the network dynamics. Results call for the examination of these oscillations in the presence of inhibition and external drives. Frontiers Media S.A. 2015-10-30 /pmc/articles/PMC4626558/ /pubmed/26578893 http://dx.doi.org/10.3389/fncir.2015.00065 Text en Copyright © 2015 Goldental, Vardi, Sardi, Sabo and Kanter. 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) or licensor 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 Goldental, Amir Vardi, Roni Sardi, Shira Sabo, Pinhas Kanter, Ido Broadband macroscopic cortical oscillations emerge from intrinsic neuronal response failures |
title | Broadband macroscopic cortical oscillations emerge from intrinsic neuronal response failures |
title_full | Broadband macroscopic cortical oscillations emerge from intrinsic neuronal response failures |
title_fullStr | Broadband macroscopic cortical oscillations emerge from intrinsic neuronal response failures |
title_full_unstemmed | Broadband macroscopic cortical oscillations emerge from intrinsic neuronal response failures |
title_short | Broadband macroscopic cortical oscillations emerge from intrinsic neuronal response failures |
title_sort | broadband macroscopic cortical oscillations emerge from intrinsic neuronal response failures |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4626558/ https://www.ncbi.nlm.nih.gov/pubmed/26578893 http://dx.doi.org/10.3389/fncir.2015.00065 |
work_keys_str_mv | AT goldentalamir broadbandmacroscopiccorticaloscillationsemergefromintrinsicneuronalresponsefailures AT vardironi broadbandmacroscopiccorticaloscillationsemergefromintrinsicneuronalresponsefailures AT sardishira broadbandmacroscopiccorticaloscillationsemergefromintrinsicneuronalresponsefailures AT sabopinhas broadbandmacroscopiccorticaloscillationsemergefromintrinsicneuronalresponsefailures AT kanterido broadbandmacroscopiccorticaloscillationsemergefromintrinsicneuronalresponsefailures |