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Temporal dynamics of normalization reweighting

For decades, neural suppression in early visual cortex has been thought to be fixed. But recent work has challenged this assumption by showing that suppression can be reweighted based on recent history; when pairs of stimuli are repeatedly presented together, suppression between them strengthens. He...

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Autores principales: Baker, Daniel H., Marinova, Daniela, Aveyard, Richard, Hargreaves, Lydia J., Renton, Alice, Castellani, Ruby, Hall, Phoebe, Harmens, Miriam, Holroyd, Georgia, Nicholson, Beth, Williams, Emily L., Hobson, Hannah M., Wade, Alex R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10615141/
https://www.ncbi.nlm.nih.gov/pubmed/37862008
http://dx.doi.org/10.1167/jov.23.12.6
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author Baker, Daniel H.
Marinova, Daniela
Aveyard, Richard
Hargreaves, Lydia J.
Renton, Alice
Castellani, Ruby
Hall, Phoebe
Harmens, Miriam
Holroyd, Georgia
Nicholson, Beth
Williams, Emily L.
Hobson, Hannah M.
Wade, Alex R.
author_facet Baker, Daniel H.
Marinova, Daniela
Aveyard, Richard
Hargreaves, Lydia J.
Renton, Alice
Castellani, Ruby
Hall, Phoebe
Harmens, Miriam
Holroyd, Georgia
Nicholson, Beth
Williams, Emily L.
Hobson, Hannah M.
Wade, Alex R.
author_sort Baker, Daniel H.
collection PubMed
description For decades, neural suppression in early visual cortex has been thought to be fixed. But recent work has challenged this assumption by showing that suppression can be reweighted based on recent history; when pairs of stimuli are repeatedly presented together, suppression between them strengthens. Here we investigate the temporal dynamics of this process using a steady-state visual evoked potential (SSVEP) paradigm that provides a time-resolved, direct index of suppression between pairs of stimuli flickering at different frequencies (5 and 7 Hz). Our initial analysis of an existing electroencephalography (EEG) dataset (N = 100) indicated that suppression increases substantially during the first 2–5 seconds of stimulus presentation (with some variation across stimulation frequency). We then collected new EEG data (N = 100) replicating this finding for both monocular and dichoptic mask arrangements in a preregistered study designed to measure reweighting. A third experiment (N = 20) used source-localized magnetoencephalography and found that these effects are apparent in primary visual cortex (V1), consistent with results from neurophysiological work. Because long-standing theories propose inhibition/excitation differences in autism, we also compared reweighting between individuals with high versus low autistic traits, and with and without an autism diagnosis, across our three datasets (total N = 220). We find no compelling differences in reweighting that are associated with autism. Our results support the normalization reweighting model and indicate that for prolonged stimulation, increases in suppression occur on the order of 2–5 seconds after stimulus onset.
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spelling pubmed-106151412023-10-31 Temporal dynamics of normalization reweighting Baker, Daniel H. Marinova, Daniela Aveyard, Richard Hargreaves, Lydia J. Renton, Alice Castellani, Ruby Hall, Phoebe Harmens, Miriam Holroyd, Georgia Nicholson, Beth Williams, Emily L. Hobson, Hannah M. Wade, Alex R. J Vis Article For decades, neural suppression in early visual cortex has been thought to be fixed. But recent work has challenged this assumption by showing that suppression can be reweighted based on recent history; when pairs of stimuli are repeatedly presented together, suppression between them strengthens. Here we investigate the temporal dynamics of this process using a steady-state visual evoked potential (SSVEP) paradigm that provides a time-resolved, direct index of suppression between pairs of stimuli flickering at different frequencies (5 and 7 Hz). Our initial analysis of an existing electroencephalography (EEG) dataset (N = 100) indicated that suppression increases substantially during the first 2–5 seconds of stimulus presentation (with some variation across stimulation frequency). We then collected new EEG data (N = 100) replicating this finding for both monocular and dichoptic mask arrangements in a preregistered study designed to measure reweighting. A third experiment (N = 20) used source-localized magnetoencephalography and found that these effects are apparent in primary visual cortex (V1), consistent with results from neurophysiological work. Because long-standing theories propose inhibition/excitation differences in autism, we also compared reweighting between individuals with high versus low autistic traits, and with and without an autism diagnosis, across our three datasets (total N = 220). We find no compelling differences in reweighting that are associated with autism. Our results support the normalization reweighting model and indicate that for prolonged stimulation, increases in suppression occur on the order of 2–5 seconds after stimulus onset. The Association for Research in Vision and Ophthalmology 2023-10-20 /pmc/articles/PMC10615141/ /pubmed/37862008 http://dx.doi.org/10.1167/jov.23.12.6 Text en Copyright 2023 The Authors https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License.
spellingShingle Article
Baker, Daniel H.
Marinova, Daniela
Aveyard, Richard
Hargreaves, Lydia J.
Renton, Alice
Castellani, Ruby
Hall, Phoebe
Harmens, Miriam
Holroyd, Georgia
Nicholson, Beth
Williams, Emily L.
Hobson, Hannah M.
Wade, Alex R.
Temporal dynamics of normalization reweighting
title Temporal dynamics of normalization reweighting
title_full Temporal dynamics of normalization reweighting
title_fullStr Temporal dynamics of normalization reweighting
title_full_unstemmed Temporal dynamics of normalization reweighting
title_short Temporal dynamics of normalization reweighting
title_sort temporal dynamics of normalization reweighting
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10615141/
https://www.ncbi.nlm.nih.gov/pubmed/37862008
http://dx.doi.org/10.1167/jov.23.12.6
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