Cargando…

Comodulation Enhances Signal Detection via Priming of Auditory Cortical Circuits

Acoustic environments are composed of complex overlapping sounds that the auditory system is required to segregate into discrete perceptual objects. The functions of distinct auditory processing stations in this challenging task are poorly understood. Here we show a direct role for mouse auditory co...

Descripción completa

Detalles Bibliográficos
Autores principales: Sollini, Joseph, Chadderton, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5148223/
https://www.ncbi.nlm.nih.gov/pubmed/27927950
http://dx.doi.org/10.1523/JNEUROSCI.0656-16.2016
_version_ 1782473807332638720
author Sollini, Joseph
Chadderton, Paul
author_facet Sollini, Joseph
Chadderton, Paul
author_sort Sollini, Joseph
collection PubMed
description Acoustic environments are composed of complex overlapping sounds that the auditory system is required to segregate into discrete perceptual objects. The functions of distinct auditory processing stations in this challenging task are poorly understood. Here we show a direct role for mouse auditory cortex in detection and segregation of acoustic information. We measured the sensitivity of auditory cortical neurons to brief tones embedded in masking noise. By altering spectrotemporal characteristics of the masker, we reveal that sensitivity to pure tone stimuli is strongly enhanced in coherently modulated broadband noise, corresponding to the psychoacoustic phenomenon comodulation masking release. Improvements in detection were largest following priming periods of noise alone, indicating that cortical segregation is enhanced over time. Transient opsin-mediated silencing of auditory cortex during the priming period almost completely abolished these improvements, suggesting that cortical processing may play a direct and significant role in detection of quiet sounds in noisy environments. SIGNIFICANCE STATEMENT Auditory systems are adept at detecting and segregating competing sound sources, but there is little direct evidence of how this process occurs in the mammalian auditory pathway. We demonstrate that coherent broadband noise enhances signal representation in auditory cortex, and that prolonged exposure to noise is necessary to produce this enhancement. Using optogenetic perturbation to selectively silence auditory cortex during early noise processing, we show that cortical processing plays a crucial role in the segregation of competing sounds.
format Online
Article
Text
id pubmed-5148223
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Society for Neuroscience
record_format MEDLINE/PubMed
spelling pubmed-51482232016-12-28 Comodulation Enhances Signal Detection via Priming of Auditory Cortical Circuits Sollini, Joseph Chadderton, Paul J Neurosci Research Articles Acoustic environments are composed of complex overlapping sounds that the auditory system is required to segregate into discrete perceptual objects. The functions of distinct auditory processing stations in this challenging task are poorly understood. Here we show a direct role for mouse auditory cortex in detection and segregation of acoustic information. We measured the sensitivity of auditory cortical neurons to brief tones embedded in masking noise. By altering spectrotemporal characteristics of the masker, we reveal that sensitivity to pure tone stimuli is strongly enhanced in coherently modulated broadband noise, corresponding to the psychoacoustic phenomenon comodulation masking release. Improvements in detection were largest following priming periods of noise alone, indicating that cortical segregation is enhanced over time. Transient opsin-mediated silencing of auditory cortex during the priming period almost completely abolished these improvements, suggesting that cortical processing may play a direct and significant role in detection of quiet sounds in noisy environments. SIGNIFICANCE STATEMENT Auditory systems are adept at detecting and segregating competing sound sources, but there is little direct evidence of how this process occurs in the mammalian auditory pathway. We demonstrate that coherent broadband noise enhances signal representation in auditory cortex, and that prolonged exposure to noise is necessary to produce this enhancement. Using optogenetic perturbation to selectively silence auditory cortex during early noise processing, we show that cortical processing plays a crucial role in the segregation of competing sounds. Society for Neuroscience 2016-12-07 /pmc/articles/PMC5148223/ /pubmed/27927950 http://dx.doi.org/10.1523/JNEUROSCI.0656-16.2016 Text en Copyright © 2016 Sollini and Chadderton https://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License Creative Commons Attribution 4.0 International (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Articles
Sollini, Joseph
Chadderton, Paul
Comodulation Enhances Signal Detection via Priming of Auditory Cortical Circuits
title Comodulation Enhances Signal Detection via Priming of Auditory Cortical Circuits
title_full Comodulation Enhances Signal Detection via Priming of Auditory Cortical Circuits
title_fullStr Comodulation Enhances Signal Detection via Priming of Auditory Cortical Circuits
title_full_unstemmed Comodulation Enhances Signal Detection via Priming of Auditory Cortical Circuits
title_short Comodulation Enhances Signal Detection via Priming of Auditory Cortical Circuits
title_sort comodulation enhances signal detection via priming of auditory cortical circuits
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5148223/
https://www.ncbi.nlm.nih.gov/pubmed/27927950
http://dx.doi.org/10.1523/JNEUROSCI.0656-16.2016
work_keys_str_mv AT sollinijoseph comodulationenhancessignaldetectionviaprimingofauditorycorticalcircuits
AT chaddertonpaul comodulationenhancessignaldetectionviaprimingofauditorycorticalcircuits