Cargando…

Speech encoding by coupled cortical theta and gamma oscillations

Many environmental stimuli present a quasi-rhythmic structure at different timescales that the brain needs to decompose and integrate. Cortical oscillations have been proposed as instruments of sensory de-multiplexing, i.e., the parallel processing of different frequency streams in sensory signals....

Descripción completa

Detalles Bibliográficos
Autores principales: Hyafil, Alexandre, Fontolan, Lorenzo, Kabdebon, Claire, Gutkin, Boris, Giraud, Anne-Lise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4480273/
https://www.ncbi.nlm.nih.gov/pubmed/26023831
http://dx.doi.org/10.7554/eLife.06213
_version_ 1782378131306315776
author Hyafil, Alexandre
Fontolan, Lorenzo
Kabdebon, Claire
Gutkin, Boris
Giraud, Anne-Lise
author_facet Hyafil, Alexandre
Fontolan, Lorenzo
Kabdebon, Claire
Gutkin, Boris
Giraud, Anne-Lise
author_sort Hyafil, Alexandre
collection PubMed
description Many environmental stimuli present a quasi-rhythmic structure at different timescales that the brain needs to decompose and integrate. Cortical oscillations have been proposed as instruments of sensory de-multiplexing, i.e., the parallel processing of different frequency streams in sensory signals. Yet their causal role in such a process has never been demonstrated. Here, we used a neural microcircuit model to address whether coupled theta–gamma oscillations, as observed in human auditory cortex, could underpin the multiscale sensory analysis of speech. We show that, in continuous speech, theta oscillations can flexibly track the syllabic rhythm and temporally organize the phoneme-level response of gamma neurons into a code that enables syllable identification. The tracking of slow speech fluctuations by theta oscillations, and its coupling to gamma-spiking activity both appeared as critical features for accurate speech encoding. These results demonstrate that cortical oscillations can be a key instrument of speech de-multiplexing, parsing, and encoding. DOI: http://dx.doi.org/10.7554/eLife.06213.001
format Online
Article
Text
id pubmed-4480273
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-44802732015-06-26 Speech encoding by coupled cortical theta and gamma oscillations Hyafil, Alexandre Fontolan, Lorenzo Kabdebon, Claire Gutkin, Boris Giraud, Anne-Lise eLife Computational and Systems Biology Many environmental stimuli present a quasi-rhythmic structure at different timescales that the brain needs to decompose and integrate. Cortical oscillations have been proposed as instruments of sensory de-multiplexing, i.e., the parallel processing of different frequency streams in sensory signals. Yet their causal role in such a process has never been demonstrated. Here, we used a neural microcircuit model to address whether coupled theta–gamma oscillations, as observed in human auditory cortex, could underpin the multiscale sensory analysis of speech. We show that, in continuous speech, theta oscillations can flexibly track the syllabic rhythm and temporally organize the phoneme-level response of gamma neurons into a code that enables syllable identification. The tracking of slow speech fluctuations by theta oscillations, and its coupling to gamma-spiking activity both appeared as critical features for accurate speech encoding. These results demonstrate that cortical oscillations can be a key instrument of speech de-multiplexing, parsing, and encoding. DOI: http://dx.doi.org/10.7554/eLife.06213.001 eLife Sciences Publications, Ltd 2015-05-29 /pmc/articles/PMC4480273/ /pubmed/26023831 http://dx.doi.org/10.7554/eLife.06213 Text en © 2015, Hyafil et al 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 Computational and Systems Biology
Hyafil, Alexandre
Fontolan, Lorenzo
Kabdebon, Claire
Gutkin, Boris
Giraud, Anne-Lise
Speech encoding by coupled cortical theta and gamma oscillations
title Speech encoding by coupled cortical theta and gamma oscillations
title_full Speech encoding by coupled cortical theta and gamma oscillations
title_fullStr Speech encoding by coupled cortical theta and gamma oscillations
title_full_unstemmed Speech encoding by coupled cortical theta and gamma oscillations
title_short Speech encoding by coupled cortical theta and gamma oscillations
title_sort speech encoding by coupled cortical theta and gamma oscillations
topic Computational and Systems Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4480273/
https://www.ncbi.nlm.nih.gov/pubmed/26023831
http://dx.doi.org/10.7554/eLife.06213
work_keys_str_mv AT hyafilalexandre speechencodingbycoupledcorticalthetaandgammaoscillations
AT fontolanlorenzo speechencodingbycoupledcorticalthetaandgammaoscillations
AT kabdebonclaire speechencodingbycoupledcorticalthetaandgammaoscillations
AT gutkinboris speechencodingbycoupledcorticalthetaandgammaoscillations
AT giraudannelise speechencodingbycoupledcorticalthetaandgammaoscillations