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Thalamocortical Mechanisms Regulating the Relationship between Transient Beta Events and Human Tactile Perception
Transient neocortical events with high spectral power in the 15–29 Hz beta band are among the most reliable predictors of sensory perception. Prestimulus beta event rates in primary somatosensory cortex correlate with sensory suppression, most effectively 100–300 ms before stimulus onset. However, t...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8841599/ https://www.ncbi.nlm.nih.gov/pubmed/34401898 http://dx.doi.org/10.1093/cercor/bhab221 |
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author | Law, Robert G Pugliese, Sarah Shin, Hyeyoung Sliva, Danielle D Lee, Shane Neymotin, Samuel Moore, Christopher Jones, Stephanie R |
author_facet | Law, Robert G Pugliese, Sarah Shin, Hyeyoung Sliva, Danielle D Lee, Shane Neymotin, Samuel Moore, Christopher Jones, Stephanie R |
author_sort | Law, Robert G |
collection | PubMed |
description | Transient neocortical events with high spectral power in the 15–29 Hz beta band are among the most reliable predictors of sensory perception. Prestimulus beta event rates in primary somatosensory cortex correlate with sensory suppression, most effectively 100–300 ms before stimulus onset. However, the neural mechanisms underlying this perceptual association are unknown. We combined human magnetoencephalography (MEG) measurements with biophysical neural modeling to test potential cellular and circuit mechanisms that underlie observed correlations between prestimulus beta events and tactile detection. Extending prior studies, we found that simulated bursts from higher-order, nonlemniscal thalamus were sufficient to drive beta event generation and to recruit slow supragranular inhibition acting on a 300 ms timescale to suppress sensory information. Further analysis showed that the same beta-generating mechanism can lead to facilitated perception for a brief period when beta events occur simultaneously with tactile stimulation before inhibition is recruited. These findings were supported by close agreement between model-derived predictions and empirical MEG data. The postevent suppressive mechanism explains an array of studies that associate beta with decreased processing, whereas the during-event facilitatory mechanism may demand a reinterpretation of the role of beta events in the context of coincident timing. |
format | Online Article Text |
id | pubmed-8841599 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-88415992022-02-14 Thalamocortical Mechanisms Regulating the Relationship between Transient Beta Events and Human Tactile Perception Law, Robert G Pugliese, Sarah Shin, Hyeyoung Sliva, Danielle D Lee, Shane Neymotin, Samuel Moore, Christopher Jones, Stephanie R Cereb Cortex Original Article Transient neocortical events with high spectral power in the 15–29 Hz beta band are among the most reliable predictors of sensory perception. Prestimulus beta event rates in primary somatosensory cortex correlate with sensory suppression, most effectively 100–300 ms before stimulus onset. However, the neural mechanisms underlying this perceptual association are unknown. We combined human magnetoencephalography (MEG) measurements with biophysical neural modeling to test potential cellular and circuit mechanisms that underlie observed correlations between prestimulus beta events and tactile detection. Extending prior studies, we found that simulated bursts from higher-order, nonlemniscal thalamus were sufficient to drive beta event generation and to recruit slow supragranular inhibition acting on a 300 ms timescale to suppress sensory information. Further analysis showed that the same beta-generating mechanism can lead to facilitated perception for a brief period when beta events occur simultaneously with tactile stimulation before inhibition is recruited. These findings were supported by close agreement between model-derived predictions and empirical MEG data. The postevent suppressive mechanism explains an array of studies that associate beta with decreased processing, whereas the during-event facilitatory mechanism may demand a reinterpretation of the role of beta events in the context of coincident timing. Oxford University Press 2021-08-16 /pmc/articles/PMC8841599/ /pubmed/34401898 http://dx.doi.org/10.1093/cercor/bhab221 Text en © The Author(s) 2021. Published by Oxford University Press. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Original Article Law, Robert G Pugliese, Sarah Shin, Hyeyoung Sliva, Danielle D Lee, Shane Neymotin, Samuel Moore, Christopher Jones, Stephanie R Thalamocortical Mechanisms Regulating the Relationship between Transient Beta Events and Human Tactile Perception |
title | Thalamocortical Mechanisms Regulating the Relationship between Transient Beta Events and Human Tactile Perception |
title_full | Thalamocortical Mechanisms Regulating the Relationship between Transient Beta Events and Human Tactile Perception |
title_fullStr | Thalamocortical Mechanisms Regulating the Relationship between Transient Beta Events and Human Tactile Perception |
title_full_unstemmed | Thalamocortical Mechanisms Regulating the Relationship between Transient Beta Events and Human Tactile Perception |
title_short | Thalamocortical Mechanisms Regulating the Relationship between Transient Beta Events and Human Tactile Perception |
title_sort | thalamocortical mechanisms regulating the relationship between transient beta events and human tactile perception |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8841599/ https://www.ncbi.nlm.nih.gov/pubmed/34401898 http://dx.doi.org/10.1093/cercor/bhab221 |
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