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Task-dependent and distinct roles of the temporoparietal junction and inferior frontal cortex in the control of imitation

The control of neurological networks supporting social cognition is crucially important for social interaction. In particular, the control of imitation is directly linked to interaction quality, with impairments associated with disorders characterized by social difficulties. Previous work suggests i...

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Autores principales: Hogeveen, Jeremy, Obhi, Sukhvinder S., Banissy, Michael J., Santiesteban, Idalmis, Press, Clare, Catmur, Caroline, Bird, Geoffrey
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4483570/
https://www.ncbi.nlm.nih.gov/pubmed/25481003
http://dx.doi.org/10.1093/scan/nsu148
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author Hogeveen, Jeremy
Obhi, Sukhvinder S.
Banissy, Michael J.
Santiesteban, Idalmis
Press, Clare
Catmur, Caroline
Bird, Geoffrey
author_facet Hogeveen, Jeremy
Obhi, Sukhvinder S.
Banissy, Michael J.
Santiesteban, Idalmis
Press, Clare
Catmur, Caroline
Bird, Geoffrey
author_sort Hogeveen, Jeremy
collection PubMed
description The control of neurological networks supporting social cognition is crucially important for social interaction. In particular, the control of imitation is directly linked to interaction quality, with impairments associated with disorders characterized by social difficulties. Previous work suggests inferior frontal cortex (IFC) and the temporoparietal junction (TPJ) are involved in controlling imitation, but the functional roles of these areas remain unclear. Here, transcranial direct current stimulation (tDCS) was used to enhance cortical excitability at IFC and the TPJ prior to the completion of three tasks: (i) a naturalistic social interaction during which increased imitation is known to improve rapport, (ii) a choice reaction time task in which imitation needs to be inhibited for successful performance and (iii) a non-imitative control task. Relative to sham stimulation, stimulating IFC improved the context-dependent control of imitation—participants imitated more during the social interaction and less during the imitation inhibition task. In contrast, stimulating the TPJ reduced imitation in the inhibition task without affecting imitation during social interaction. Neither stimulation site affected the non-imitative control task. These data support a model in which IFC modulates imitation directly according to task demands, whereas TPJ controls task-appropriate shifts in attention toward representation of the self or the other, indirectly impacting upon imitation.
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spelling pubmed-44835702015-06-30 Task-dependent and distinct roles of the temporoparietal junction and inferior frontal cortex in the control of imitation Hogeveen, Jeremy Obhi, Sukhvinder S. Banissy, Michael J. Santiesteban, Idalmis Press, Clare Catmur, Caroline Bird, Geoffrey Soc Cogn Affect Neurosci Original Articles The control of neurological networks supporting social cognition is crucially important for social interaction. In particular, the control of imitation is directly linked to interaction quality, with impairments associated with disorders characterized by social difficulties. Previous work suggests inferior frontal cortex (IFC) and the temporoparietal junction (TPJ) are involved in controlling imitation, but the functional roles of these areas remain unclear. Here, transcranial direct current stimulation (tDCS) was used to enhance cortical excitability at IFC and the TPJ prior to the completion of three tasks: (i) a naturalistic social interaction during which increased imitation is known to improve rapport, (ii) a choice reaction time task in which imitation needs to be inhibited for successful performance and (iii) a non-imitative control task. Relative to sham stimulation, stimulating IFC improved the context-dependent control of imitation—participants imitated more during the social interaction and less during the imitation inhibition task. In contrast, stimulating the TPJ reduced imitation in the inhibition task without affecting imitation during social interaction. Neither stimulation site affected the non-imitative control task. These data support a model in which IFC modulates imitation directly according to task demands, whereas TPJ controls task-appropriate shifts in attention toward representation of the self or the other, indirectly impacting upon imitation. Oxford University Press 2015-07 2014-12-05 /pmc/articles/PMC4483570/ /pubmed/25481003 http://dx.doi.org/10.1093/scan/nsu148 Text en © The Author (2014). Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Hogeveen, Jeremy
Obhi, Sukhvinder S.
Banissy, Michael J.
Santiesteban, Idalmis
Press, Clare
Catmur, Caroline
Bird, Geoffrey
Task-dependent and distinct roles of the temporoparietal junction and inferior frontal cortex in the control of imitation
title Task-dependent and distinct roles of the temporoparietal junction and inferior frontal cortex in the control of imitation
title_full Task-dependent and distinct roles of the temporoparietal junction and inferior frontal cortex in the control of imitation
title_fullStr Task-dependent and distinct roles of the temporoparietal junction and inferior frontal cortex in the control of imitation
title_full_unstemmed Task-dependent and distinct roles of the temporoparietal junction and inferior frontal cortex in the control of imitation
title_short Task-dependent and distinct roles of the temporoparietal junction and inferior frontal cortex in the control of imitation
title_sort task-dependent and distinct roles of the temporoparietal junction and inferior frontal cortex in the control of imitation
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4483570/
https://www.ncbi.nlm.nih.gov/pubmed/25481003
http://dx.doi.org/10.1093/scan/nsu148
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