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Auditory cortex modelled as a dynamical network of oscillators: understanding event-related fields and their adaptation
Adaptation, the reduction of neuronal responses by repetitive stimulation, is a ubiquitous feature of auditory cortex (AC). It is not clear what causes adaptation, but short-term synaptic depression (STSD) is a potential candidate for the underlying mechanism. In such a case, adaptation can be direc...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9287241/ https://www.ncbi.nlm.nih.gov/pubmed/35718809 http://dx.doi.org/10.1007/s00422-022-00936-7 |
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author | Hajizadeh, Aida Matysiak, Artur Wolfrum, Matthias May, Patrick J. C. König, Reinhard |
author_facet | Hajizadeh, Aida Matysiak, Artur Wolfrum, Matthias May, Patrick J. C. König, Reinhard |
author_sort | Hajizadeh, Aida |
collection | PubMed |
description | Adaptation, the reduction of neuronal responses by repetitive stimulation, is a ubiquitous feature of auditory cortex (AC). It is not clear what causes adaptation, but short-term synaptic depression (STSD) is a potential candidate for the underlying mechanism. In such a case, adaptation can be directly linked with the way AC produces context-sensitive responses such as mismatch negativity and stimulus-specific adaptation observed on the single-unit level. We examined this hypothesis via a computational model based on AC anatomy, which includes serially connected core, belt, and parabelt areas. The model replicates the event-related field (ERF) of the magnetoencephalogram as well as ERF adaptation. The model dynamics are described by excitatory and inhibitory state variables of cell populations, with the excitatory connections modulated by STSD. We analysed the system dynamics by linearising the firing rates and solving the STSD equation using time-scale separation. This allows for characterisation of AC dynamics as a superposition of damped harmonic oscillators, so-called normal modes. We show that repetition suppression of the N1m is due to a mixture of causes, with stimulus repetition modifying both the amplitudes and the frequencies of the normal modes. In this view, adaptation results from a complete reorganisation of AC dynamics rather than a reduction of activity in discrete sources. Further, both the network structure and the balance between excitation and inhibition contribute significantly to the rate with which AC recovers from adaptation. This lifetime of adaptation is longer in the belt and parabelt than in the core area, despite the time constants of STSD being spatially homogeneous. Finally, we critically evaluate the use of a single exponential function to describe recovery from adaptation. |
format | Online Article Text |
id | pubmed-9287241 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-92872412022-07-17 Auditory cortex modelled as a dynamical network of oscillators: understanding event-related fields and their adaptation Hajizadeh, Aida Matysiak, Artur Wolfrum, Matthias May, Patrick J. C. König, Reinhard Biol Cybern Original Article Adaptation, the reduction of neuronal responses by repetitive stimulation, is a ubiquitous feature of auditory cortex (AC). It is not clear what causes adaptation, but short-term synaptic depression (STSD) is a potential candidate for the underlying mechanism. In such a case, adaptation can be directly linked with the way AC produces context-sensitive responses such as mismatch negativity and stimulus-specific adaptation observed on the single-unit level. We examined this hypothesis via a computational model based on AC anatomy, which includes serially connected core, belt, and parabelt areas. The model replicates the event-related field (ERF) of the magnetoencephalogram as well as ERF adaptation. The model dynamics are described by excitatory and inhibitory state variables of cell populations, with the excitatory connections modulated by STSD. We analysed the system dynamics by linearising the firing rates and solving the STSD equation using time-scale separation. This allows for characterisation of AC dynamics as a superposition of damped harmonic oscillators, so-called normal modes. We show that repetition suppression of the N1m is due to a mixture of causes, with stimulus repetition modifying both the amplitudes and the frequencies of the normal modes. In this view, adaptation results from a complete reorganisation of AC dynamics rather than a reduction of activity in discrete sources. Further, both the network structure and the balance between excitation and inhibition contribute significantly to the rate with which AC recovers from adaptation. This lifetime of adaptation is longer in the belt and parabelt than in the core area, despite the time constants of STSD being spatially homogeneous. Finally, we critically evaluate the use of a single exponential function to describe recovery from adaptation. Springer Berlin Heidelberg 2022-06-20 2022 /pmc/articles/PMC9287241/ /pubmed/35718809 http://dx.doi.org/10.1007/s00422-022-00936-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Hajizadeh, Aida Matysiak, Artur Wolfrum, Matthias May, Patrick J. C. König, Reinhard Auditory cortex modelled as a dynamical network of oscillators: understanding event-related fields and their adaptation |
title | Auditory cortex modelled as a dynamical network of oscillators: understanding event-related fields and their adaptation |
title_full | Auditory cortex modelled as a dynamical network of oscillators: understanding event-related fields and their adaptation |
title_fullStr | Auditory cortex modelled as a dynamical network of oscillators: understanding event-related fields and their adaptation |
title_full_unstemmed | Auditory cortex modelled as a dynamical network of oscillators: understanding event-related fields and their adaptation |
title_short | Auditory cortex modelled as a dynamical network of oscillators: understanding event-related fields and their adaptation |
title_sort | auditory cortex modelled as a dynamical network of oscillators: understanding event-related fields and their adaptation |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9287241/ https://www.ncbi.nlm.nih.gov/pubmed/35718809 http://dx.doi.org/10.1007/s00422-022-00936-7 |
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