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High‐gamma oscillations precede visual steady‐state responses: A human electrocorticography study
The robust steady‐state cortical activation elicited by flickering visual stimulation has been exploited by a wide range of scientific studies. As the fundamental neural response inherits the spectral properties of the gazed flickering, the paradigm has been used to chart cortical characteristics an...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7670637/ https://www.ncbi.nlm.nih.gov/pubmed/32885895 http://dx.doi.org/10.1002/hbm.25196 |
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author | Wittevrongel, Benjamin Khachatryan, Elvira Carrette, Evelien Boon, Paul Meurs, Alfred Van Roost, Dirk Van Hulle, Marc M. |
author_facet | Wittevrongel, Benjamin Khachatryan, Elvira Carrette, Evelien Boon, Paul Meurs, Alfred Van Roost, Dirk Van Hulle, Marc M. |
author_sort | Wittevrongel, Benjamin |
collection | PubMed |
description | The robust steady‐state cortical activation elicited by flickering visual stimulation has been exploited by a wide range of scientific studies. As the fundamental neural response inherits the spectral properties of the gazed flickering, the paradigm has been used to chart cortical characteristics and their relation to pathologies. However, despite its widespread adoption, the underlying neural mechanisms are not well understood. Here, we show that the fundamental response is preceded by high‐gamma (55–125 Hz) oscillations which are also synchronised to the gazed frequency. Using a subdural recording of the primary and associative visual cortices of one human subject, we demonstrate that the latencies of the high‐gamma and fundamental components are highly correlated on a single‐trial basis albeit that the latter is consistently delayed by approximately 55 ms. These results corroborate previous reports that top‐down feedback projections are involved in the generation of the fundamental response, but, in addition, we show that trial‐to‐trial variability in fundamental latency is paralleled by a highly similar variability in high‐gamma latency. Pathology‐ or paradigm‐induced alterations in steady‐state responses could thus originate either from deviating visual gamma responses or from aberrations in the neural feedback mechanism. Experiments designed to tease apart the two processes are expected to provide deeper insights into the studied paradigm. |
format | Online Article Text |
id | pubmed-7670637 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-76706372020-11-23 High‐gamma oscillations precede visual steady‐state responses: A human electrocorticography study Wittevrongel, Benjamin Khachatryan, Elvira Carrette, Evelien Boon, Paul Meurs, Alfred Van Roost, Dirk Van Hulle, Marc M. Hum Brain Mapp Research Articles The robust steady‐state cortical activation elicited by flickering visual stimulation has been exploited by a wide range of scientific studies. As the fundamental neural response inherits the spectral properties of the gazed flickering, the paradigm has been used to chart cortical characteristics and their relation to pathologies. However, despite its widespread adoption, the underlying neural mechanisms are not well understood. Here, we show that the fundamental response is preceded by high‐gamma (55–125 Hz) oscillations which are also synchronised to the gazed frequency. Using a subdural recording of the primary and associative visual cortices of one human subject, we demonstrate that the latencies of the high‐gamma and fundamental components are highly correlated on a single‐trial basis albeit that the latter is consistently delayed by approximately 55 ms. These results corroborate previous reports that top‐down feedback projections are involved in the generation of the fundamental response, but, in addition, we show that trial‐to‐trial variability in fundamental latency is paralleled by a highly similar variability in high‐gamma latency. Pathology‐ or paradigm‐induced alterations in steady‐state responses could thus originate either from deviating visual gamma responses or from aberrations in the neural feedback mechanism. Experiments designed to tease apart the two processes are expected to provide deeper insights into the studied paradigm. John Wiley & Sons, Inc. 2020-09-04 /pmc/articles/PMC7670637/ /pubmed/32885895 http://dx.doi.org/10.1002/hbm.25196 Text en © 2020 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Wittevrongel, Benjamin Khachatryan, Elvira Carrette, Evelien Boon, Paul Meurs, Alfred Van Roost, Dirk Van Hulle, Marc M. High‐gamma oscillations precede visual steady‐state responses: A human electrocorticography study |
title | High‐gamma oscillations precede visual steady‐state responses: A human electrocorticography study |
title_full | High‐gamma oscillations precede visual steady‐state responses: A human electrocorticography study |
title_fullStr | High‐gamma oscillations precede visual steady‐state responses: A human electrocorticography study |
title_full_unstemmed | High‐gamma oscillations precede visual steady‐state responses: A human electrocorticography study |
title_short | High‐gamma oscillations precede visual steady‐state responses: A human electrocorticography study |
title_sort | high‐gamma oscillations precede visual steady‐state responses: a human electrocorticography study |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7670637/ https://www.ncbi.nlm.nih.gov/pubmed/32885895 http://dx.doi.org/10.1002/hbm.25196 |
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