Top-down beta rhythms support selective attention via interlaminar interaction: a model.

Cortical rhythms have been thought to play crucial roles in our cognitive abilities. Rhythmic activity in the beta frequency band, around 20 Hz, has been reported in recent studies that focused on neural correlates of attention, indicating that top-down beta rhythms, generated in higher cognitive ar...

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Autores principales: Jung H Lee, Miles A Whittington, Nancy J Kopell
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Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2013
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Acceso en línea:https://doaj.org/article/ba47d188b72044759bd6fbf528f80d2d
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spelling oai:doaj.org-article:ba47d188b72044759bd6fbf528f80d2d2021-11-18T05:53:41ZTop-down beta rhythms support selective attention via interlaminar interaction: a model.1553-734X1553-735810.1371/journal.pcbi.1003164https://doaj.org/article/ba47d188b72044759bd6fbf528f80d2d2013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23950699/pdf/?tool=EBIhttps://doaj.org/toc/1553-734Xhttps://doaj.org/toc/1553-7358Cortical rhythms have been thought to play crucial roles in our cognitive abilities. Rhythmic activity in the beta frequency band, around 20 Hz, has been reported in recent studies that focused on neural correlates of attention, indicating that top-down beta rhythms, generated in higher cognitive areas and delivered to earlier sensory areas, can support attentional gain modulation. To elucidate functional roles of beta rhythms and underlying mechanisms, we built a computational model of sensory cortical areas. Our simulation results show that top-down beta rhythms can activate ascending synaptic projections from L5 to L4 and L2/3, responsible for biased competition in superficial layers. In the simulation, slow-inhibitory interneurons are shown to resonate to the 20 Hz input and modulate the activity in superficial layers in an attention-related manner. The predicted critical roles of these cells in attentional gain provide a potential mechanism by which cholinergic drive can support selective attention.Jung H LeeMiles A WhittingtonNancy J KopellPublic Library of Science (PLoS)articleBiology (General)QH301-705.5ENPLoS Computational Biology, Vol 9, Iss 8, p e1003164 (2013)
institution DOAJ
collection DOAJ
language EN
topic Biology (General)
QH301-705.5
spellingShingle Biology (General)
QH301-705.5
Jung H Lee
Miles A Whittington
Nancy J Kopell
Top-down beta rhythms support selective attention via interlaminar interaction: a model.
description Cortical rhythms have been thought to play crucial roles in our cognitive abilities. Rhythmic activity in the beta frequency band, around 20 Hz, has been reported in recent studies that focused on neural correlates of attention, indicating that top-down beta rhythms, generated in higher cognitive areas and delivered to earlier sensory areas, can support attentional gain modulation. To elucidate functional roles of beta rhythms and underlying mechanisms, we built a computational model of sensory cortical areas. Our simulation results show that top-down beta rhythms can activate ascending synaptic projections from L5 to L4 and L2/3, responsible for biased competition in superficial layers. In the simulation, slow-inhibitory interneurons are shown to resonate to the 20 Hz input and modulate the activity in superficial layers in an attention-related manner. The predicted critical roles of these cells in attentional gain provide a potential mechanism by which cholinergic drive can support selective attention.
format article
author Jung H Lee
Miles A Whittington
Nancy J Kopell
author_facet Jung H Lee
Miles A Whittington
Nancy J Kopell
author_sort Jung H Lee
title Top-down beta rhythms support selective attention via interlaminar interaction: a model.
title_short Top-down beta rhythms support selective attention via interlaminar interaction: a model.
title_full Top-down beta rhythms support selective attention via interlaminar interaction: a model.
title_fullStr Top-down beta rhythms support selective attention via interlaminar interaction: a model.
title_full_unstemmed Top-down beta rhythms support selective attention via interlaminar interaction: a model.
title_sort top-down beta rhythms support selective attention via interlaminar interaction: a model.
publisher Public Library of Science (PLoS)
publishDate 2013
url https://doaj.org/article/ba47d188b72044759bd6fbf528f80d2d
work_keys_str_mv AT junghlee topdownbetarhythmssupportselectiveattentionviainterlaminarinteractionamodel
AT milesawhittington topdownbetarhythmssupportselectiveattentionviainterlaminarinteractionamodel
AT nancyjkopell topdownbetarhythmssupportselectiveattentionviainterlaminarinteractionamodel
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