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Brain Networks of Novelty-Driven Involuntary and Cued Voluntary Auditory Attention Shifting

In everyday life, we need a capacity to flexibly shift attention between alternative sound sources. However, relatively little work has been done to elucidate the mechanisms of attention shifting in the auditory domain. Here, we used a mixed event-related/sparse-sampling fMRI approach to investigate...

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Detalles Bibliográficos
Autores principales: Huang, Samantha, Belliveau, John W., Tengshe, Chinmayi, Ahveninen, Jyrki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3429427/
https://www.ncbi.nlm.nih.gov/pubmed/22937153
http://dx.doi.org/10.1371/journal.pone.0044062
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author Huang, Samantha
Belliveau, John W.
Tengshe, Chinmayi
Ahveninen, Jyrki
author_facet Huang, Samantha
Belliveau, John W.
Tengshe, Chinmayi
Ahveninen, Jyrki
author_sort Huang, Samantha
collection PubMed
description In everyday life, we need a capacity to flexibly shift attention between alternative sound sources. However, relatively little work has been done to elucidate the mechanisms of attention shifting in the auditory domain. Here, we used a mixed event-related/sparse-sampling fMRI approach to investigate this essential cognitive function. In each 10-sec trial, subjects were instructed to wait for an auditory “cue” signaling the location where a subsequent “target” sound was likely to be presented. The target was occasionally replaced by an unexpected “novel” sound in the uncued ear, to trigger involuntary attention shifting. To maximize the attention effects, cues, targets, and novels were embedded within dichotic 800-Hz vs. 1500-Hz pure-tone “standard” trains. The sound of clustered fMRI acquisition (starting at t = 7.82 sec) served as a controlled trial-end signal. Our approach revealed notable activation differences between the conditions. Cued voluntary attention shifting activated the superior intra­­parietal sulcus (IPS), whereas novelty-triggered involuntary orienting activated the inferior IPS and certain subareas of the precuneus. Clearly more widespread activations were observed during voluntary than involuntary orienting in the premotor cortex, including the frontal eye fields. Moreover, we found ­evidence for a frontoinsular-cingular attentional control network, consisting of the anterior insula, inferior frontal cortex, and medial frontal cortices, which were activated during both target discrimination and voluntary attention shifting. Finally, novels and targets activated much wider areas of superior temporal auditory cortices than shifting cues.
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spelling pubmed-34294272012-08-30 Brain Networks of Novelty-Driven Involuntary and Cued Voluntary Auditory Attention Shifting Huang, Samantha Belliveau, John W. Tengshe, Chinmayi Ahveninen, Jyrki PLoS One Research Article In everyday life, we need a capacity to flexibly shift attention between alternative sound sources. However, relatively little work has been done to elucidate the mechanisms of attention shifting in the auditory domain. Here, we used a mixed event-related/sparse-sampling fMRI approach to investigate this essential cognitive function. In each 10-sec trial, subjects were instructed to wait for an auditory “cue” signaling the location where a subsequent “target” sound was likely to be presented. The target was occasionally replaced by an unexpected “novel” sound in the uncued ear, to trigger involuntary attention shifting. To maximize the attention effects, cues, targets, and novels were embedded within dichotic 800-Hz vs. 1500-Hz pure-tone “standard” trains. The sound of clustered fMRI acquisition (starting at t = 7.82 sec) served as a controlled trial-end signal. Our approach revealed notable activation differences between the conditions. Cued voluntary attention shifting activated the superior intra­­parietal sulcus (IPS), whereas novelty-triggered involuntary orienting activated the inferior IPS and certain subareas of the precuneus. Clearly more widespread activations were observed during voluntary than involuntary orienting in the premotor cortex, including the frontal eye fields. Moreover, we found ­evidence for a frontoinsular-cingular attentional control network, consisting of the anterior insula, inferior frontal cortex, and medial frontal cortices, which were activated during both target discrimination and voluntary attention shifting. Finally, novels and targets activated much wider areas of superior temporal auditory cortices than shifting cues. Public Library of Science 2012-08-28 /pmc/articles/PMC3429427/ /pubmed/22937153 http://dx.doi.org/10.1371/journal.pone.0044062 Text en © 2012 Huang et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Huang, Samantha
Belliveau, John W.
Tengshe, Chinmayi
Ahveninen, Jyrki
Brain Networks of Novelty-Driven Involuntary and Cued Voluntary Auditory Attention Shifting
title Brain Networks of Novelty-Driven Involuntary and Cued Voluntary Auditory Attention Shifting
title_full Brain Networks of Novelty-Driven Involuntary and Cued Voluntary Auditory Attention Shifting
title_fullStr Brain Networks of Novelty-Driven Involuntary and Cued Voluntary Auditory Attention Shifting
title_full_unstemmed Brain Networks of Novelty-Driven Involuntary and Cued Voluntary Auditory Attention Shifting
title_short Brain Networks of Novelty-Driven Involuntary and Cued Voluntary Auditory Attention Shifting
title_sort brain networks of novelty-driven involuntary and cued voluntary auditory attention shifting
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3429427/
https://www.ncbi.nlm.nih.gov/pubmed/22937153
http://dx.doi.org/10.1371/journal.pone.0044062
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