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Brain activity dynamics in human parietal regions during spontaneous switches in bistable perception

The neural mechanisms underlying conscious visual perception have been extensively investigated using bistable perception paradigms. Previous functional magnetic resonance imaging (fMRI) and transcranial magnetic stimulation (TMS) studies suggest that the right anterior superior parietal (r-aSPL) an...

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Detalles Bibliográficos
Autores principales: Megumi, Fukuda, Bahrami, Bahador, Kanai, Ryota, Rees, Geraint
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4306523/
https://www.ncbi.nlm.nih.gov/pubmed/25512040
http://dx.doi.org/10.1016/j.neuroimage.2014.12.018
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author Megumi, Fukuda
Bahrami, Bahador
Kanai, Ryota
Rees, Geraint
author_facet Megumi, Fukuda
Bahrami, Bahador
Kanai, Ryota
Rees, Geraint
author_sort Megumi, Fukuda
collection PubMed
description The neural mechanisms underlying conscious visual perception have been extensively investigated using bistable perception paradigms. Previous functional magnetic resonance imaging (fMRI) and transcranial magnetic stimulation (TMS) studies suggest that the right anterior superior parietal (r-aSPL) and the right posterior superior parietal lobule (r-pSPL) have opposite roles in triggering perceptual reversals. It has been proposed that these two areas are part of a hierarchical network whose dynamics determine perceptual switches. However, how these two parietal regions interact with each other and with the rest of the brain during bistable perception is not known. Here, we investigated such a model by recording brain activity using fMRI while participants viewed a bistable structure-from-motion stimulus. Using dynamic causal modeling (DCM), we found that resolving such perceptual ambiguity was specifically associated with reciprocal interactions between these parietal regions and V5/MT. Strikingly, the strength of bottom-up coupling between V5/MT to r-pSPL and from r-pSPL to r-aSPL predicted individual mean dominance duration. Our findings are consistent with a hierarchical predictive coding model of parietal involvement in bistable perception and suggest that visual information processing underlying spontaneous perceptual switches can be described as changes in connectivity strength between parietal and visual cortical regions.
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spelling pubmed-43065232015-02-15 Brain activity dynamics in human parietal regions during spontaneous switches in bistable perception Megumi, Fukuda Bahrami, Bahador Kanai, Ryota Rees, Geraint Neuroimage Article The neural mechanisms underlying conscious visual perception have been extensively investigated using bistable perception paradigms. Previous functional magnetic resonance imaging (fMRI) and transcranial magnetic stimulation (TMS) studies suggest that the right anterior superior parietal (r-aSPL) and the right posterior superior parietal lobule (r-pSPL) have opposite roles in triggering perceptual reversals. It has been proposed that these two areas are part of a hierarchical network whose dynamics determine perceptual switches. However, how these two parietal regions interact with each other and with the rest of the brain during bistable perception is not known. Here, we investigated such a model by recording brain activity using fMRI while participants viewed a bistable structure-from-motion stimulus. Using dynamic causal modeling (DCM), we found that resolving such perceptual ambiguity was specifically associated with reciprocal interactions between these parietal regions and V5/MT. Strikingly, the strength of bottom-up coupling between V5/MT to r-pSPL and from r-pSPL to r-aSPL predicted individual mean dominance duration. Our findings are consistent with a hierarchical predictive coding model of parietal involvement in bistable perception and suggest that visual information processing underlying spontaneous perceptual switches can be described as changes in connectivity strength between parietal and visual cortical regions. Academic Press 2015-02-15 /pmc/articles/PMC4306523/ /pubmed/25512040 http://dx.doi.org/10.1016/j.neuroimage.2014.12.018 Text en © 2014 The Authors http://creativecommons.org/licenses/by/3.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Megumi, Fukuda
Bahrami, Bahador
Kanai, Ryota
Rees, Geraint
Brain activity dynamics in human parietal regions during spontaneous switches in bistable perception
title Brain activity dynamics in human parietal regions during spontaneous switches in bistable perception
title_full Brain activity dynamics in human parietal regions during spontaneous switches in bistable perception
title_fullStr Brain activity dynamics in human parietal regions during spontaneous switches in bistable perception
title_full_unstemmed Brain activity dynamics in human parietal regions during spontaneous switches in bistable perception
title_short Brain activity dynamics in human parietal regions during spontaneous switches in bistable perception
title_sort brain activity dynamics in human parietal regions during spontaneous switches in bistable perception
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4306523/
https://www.ncbi.nlm.nih.gov/pubmed/25512040
http://dx.doi.org/10.1016/j.neuroimage.2014.12.018
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