Cargando…
Top-down modulation of ventral occipito-temporal responses during visual word recognition
Although interactivity is considered a fundamental principle of cognitive (and computational) models of reading, it has received far less attention in neural models of reading that instead focus on serial stages of feed-forward processing from visual input to orthographic processing to accessing the...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Academic Press
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3221051/ https://www.ncbi.nlm.nih.gov/pubmed/21232615 http://dx.doi.org/10.1016/j.neuroimage.2011.01.001 |
_version_ | 1782217027135471616 |
---|---|
author | Twomey, Tae Kawabata Duncan, Keith J. Price, Cathy J. Devlin, Joseph T. |
author_facet | Twomey, Tae Kawabata Duncan, Keith J. Price, Cathy J. Devlin, Joseph T. |
author_sort | Twomey, Tae |
collection | PubMed |
description | Although interactivity is considered a fundamental principle of cognitive (and computational) models of reading, it has received far less attention in neural models of reading that instead focus on serial stages of feed-forward processing from visual input to orthographic processing to accessing the corresponding phonological and semantic information. In particular, the left ventral occipito-temporal (vOT) cortex is proposed to be the first stage where visual word recognition occurs prior to accessing nonvisual information such as semantics and phonology. We used functional magnetic resonance imaging (fMRI) to investigate whether there is evidence that activation in vOT is influenced top-down by the interaction of visual and nonvisual properties of the stimuli during visual word recognition tasks. Participants performed two different types of lexical decision tasks that focused on either visual or nonvisual properties of the word or word-like stimuli. The design allowed us to investigate how vOT activation during visual word recognition was influenced by a task change to the same stimuli and by a stimulus change during the same task. We found both stimulus- and task-driven modulation of vOT activation that can only be explained by top-down processing of nonvisual aspects of the task and stimuli. Our results are consistent with the hypothesis that vOT acts as an interface linking visual form with nonvisual processing in both bottom up and top down directions. Such interactive processing at the neural level is in agreement with cognitive and computational models of reading but challenges some of the assumptions made by current neuro-anatomical models of reading. |
format | Online Article Text |
id | pubmed-3221051 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Academic Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-32210512011-12-23 Top-down modulation of ventral occipito-temporal responses during visual word recognition Twomey, Tae Kawabata Duncan, Keith J. Price, Cathy J. Devlin, Joseph T. Neuroimage Article Although interactivity is considered a fundamental principle of cognitive (and computational) models of reading, it has received far less attention in neural models of reading that instead focus on serial stages of feed-forward processing from visual input to orthographic processing to accessing the corresponding phonological and semantic information. In particular, the left ventral occipito-temporal (vOT) cortex is proposed to be the first stage where visual word recognition occurs prior to accessing nonvisual information such as semantics and phonology. We used functional magnetic resonance imaging (fMRI) to investigate whether there is evidence that activation in vOT is influenced top-down by the interaction of visual and nonvisual properties of the stimuli during visual word recognition tasks. Participants performed two different types of lexical decision tasks that focused on either visual or nonvisual properties of the word or word-like stimuli. The design allowed us to investigate how vOT activation during visual word recognition was influenced by a task change to the same stimuli and by a stimulus change during the same task. We found both stimulus- and task-driven modulation of vOT activation that can only be explained by top-down processing of nonvisual aspects of the task and stimuli. Our results are consistent with the hypothesis that vOT acts as an interface linking visual form with nonvisual processing in both bottom up and top down directions. Such interactive processing at the neural level is in agreement with cognitive and computational models of reading but challenges some of the assumptions made by current neuro-anatomical models of reading. Academic Press 2011-04-01 /pmc/articles/PMC3221051/ /pubmed/21232615 http://dx.doi.org/10.1016/j.neuroimage.2011.01.001 Text en © 2011 Elsevier Inc. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license |
spellingShingle | Article Twomey, Tae Kawabata Duncan, Keith J. Price, Cathy J. Devlin, Joseph T. Top-down modulation of ventral occipito-temporal responses during visual word recognition |
title | Top-down modulation of ventral occipito-temporal responses during visual word recognition |
title_full | Top-down modulation of ventral occipito-temporal responses during visual word recognition |
title_fullStr | Top-down modulation of ventral occipito-temporal responses during visual word recognition |
title_full_unstemmed | Top-down modulation of ventral occipito-temporal responses during visual word recognition |
title_short | Top-down modulation of ventral occipito-temporal responses during visual word recognition |
title_sort | top-down modulation of ventral occipito-temporal responses during visual word recognition |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3221051/ https://www.ncbi.nlm.nih.gov/pubmed/21232615 http://dx.doi.org/10.1016/j.neuroimage.2011.01.001 |
work_keys_str_mv | AT twomeytae topdownmodulationofventraloccipitotemporalresponsesduringvisualwordrecognition AT kawabataduncankeithj topdownmodulationofventraloccipitotemporalresponsesduringvisualwordrecognition AT pricecathyj topdownmodulationofventraloccipitotemporalresponsesduringvisualwordrecognition AT devlinjosepht topdownmodulationofventraloccipitotemporalresponsesduringvisualwordrecognition |