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Spatiotemporal dynamics across visual cortical laminae support a predictive coding framework for interpreting mismatch responses
Context modulates neocortical processing of sensory data. Unexpected visual stimuli elicit large responses in primary visual cortex (V1) -- a phenomenon known as deviance detection (DD) at the neural level, or “mismatch negativity” (MMN) when measured with EEG. It remains unclear how visual DD/MMN s...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10153128/ https://www.ncbi.nlm.nih.gov/pubmed/37131642 http://dx.doi.org/10.1101/2023.04.17.537173 |
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author | Gallimore, Connor G. Ricci, David Hamm, Jordan P. |
author_facet | Gallimore, Connor G. Ricci, David Hamm, Jordan P. |
author_sort | Gallimore, Connor G. |
collection | PubMed |
description | Context modulates neocortical processing of sensory data. Unexpected visual stimuli elicit large responses in primary visual cortex (V1) -- a phenomenon known as deviance detection (DD) at the neural level, or “mismatch negativity” (MMN) when measured with EEG. It remains unclear how visual DD/MMN signals emerge across cortical layers, in temporal relation to the onset of deviant stimuli, and with respect to brain oscillations. Here we employed a visual “oddball” sequence – a classic paradigm for studying aberrant DD/MMN in neuropsychiatric populations – and recorded local field potentials in V1 of awake mice with 16-channel multielectrode arrays. Multiunit activity and current source density profiles showed that while basic adaptation to redundant stimuli was present early (50ms) in layer 4 responses, DD emerged later (150–230ms) in supragranular layers (L2/3). This DD signal coincided with increased delta/theta (2–7Hz) and high-gamma (70–80Hz) oscillations in L2/3 and decreased beta oscillations (26–36hz) in L1. These results clarify the neocortical dynamics elicited during an oddball paradigm at a microcircuit level. They are consistent with a predictive coding framework, which posits that predictive suppression is present in cortical feed-back circuits, which synapse in L1, while “prediction errors” engage cortical feed-forward processing streams, which emanate from L2/3. |
format | Online Article Text |
id | pubmed-10153128 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-101531282023-05-03 Spatiotemporal dynamics across visual cortical laminae support a predictive coding framework for interpreting mismatch responses Gallimore, Connor G. Ricci, David Hamm, Jordan P. bioRxiv Article Context modulates neocortical processing of sensory data. Unexpected visual stimuli elicit large responses in primary visual cortex (V1) -- a phenomenon known as deviance detection (DD) at the neural level, or “mismatch negativity” (MMN) when measured with EEG. It remains unclear how visual DD/MMN signals emerge across cortical layers, in temporal relation to the onset of deviant stimuli, and with respect to brain oscillations. Here we employed a visual “oddball” sequence – a classic paradigm for studying aberrant DD/MMN in neuropsychiatric populations – and recorded local field potentials in V1 of awake mice with 16-channel multielectrode arrays. Multiunit activity and current source density profiles showed that while basic adaptation to redundant stimuli was present early (50ms) in layer 4 responses, DD emerged later (150–230ms) in supragranular layers (L2/3). This DD signal coincided with increased delta/theta (2–7Hz) and high-gamma (70–80Hz) oscillations in L2/3 and decreased beta oscillations (26–36hz) in L1. These results clarify the neocortical dynamics elicited during an oddball paradigm at a microcircuit level. They are consistent with a predictive coding framework, which posits that predictive suppression is present in cortical feed-back circuits, which synapse in L1, while “prediction errors” engage cortical feed-forward processing streams, which emanate from L2/3. Cold Spring Harbor Laboratory 2023-04-17 /pmc/articles/PMC10153128/ /pubmed/37131642 http://dx.doi.org/10.1101/2023.04.17.537173 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Gallimore, Connor G. Ricci, David Hamm, Jordan P. Spatiotemporal dynamics across visual cortical laminae support a predictive coding framework for interpreting mismatch responses |
title | Spatiotemporal dynamics across visual cortical laminae support a predictive coding framework for interpreting mismatch responses |
title_full | Spatiotemporal dynamics across visual cortical laminae support a predictive coding framework for interpreting mismatch responses |
title_fullStr | Spatiotemporal dynamics across visual cortical laminae support a predictive coding framework for interpreting mismatch responses |
title_full_unstemmed | Spatiotemporal dynamics across visual cortical laminae support a predictive coding framework for interpreting mismatch responses |
title_short | Spatiotemporal dynamics across visual cortical laminae support a predictive coding framework for interpreting mismatch responses |
title_sort | spatiotemporal dynamics across visual cortical laminae support a predictive coding framework for interpreting mismatch responses |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10153128/ https://www.ncbi.nlm.nih.gov/pubmed/37131642 http://dx.doi.org/10.1101/2023.04.17.537173 |
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