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Sensorimotor Alpha Activity is Modulated in Response to the Observation of Pain in Others

The perception–action account of empathy states that observation of another person's state automatically activates a similar state in the observer. It is still unclear in what way ongoing sensorimotor alpha oscillations are involved in this process. Although they have been repeatedly implicated...

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Autores principales: Whitmarsh, Stephen, Nieuwenhuis, Ingrid L. C., Barendregt, Henk P., Jensen, Ole
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3188815/
https://www.ncbi.nlm.nih.gov/pubmed/22007165
http://dx.doi.org/10.3389/fnhum.2011.00091
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author Whitmarsh, Stephen
Nieuwenhuis, Ingrid L. C.
Barendregt, Henk P.
Jensen, Ole
author_facet Whitmarsh, Stephen
Nieuwenhuis, Ingrid L. C.
Barendregt, Henk P.
Jensen, Ole
author_sort Whitmarsh, Stephen
collection PubMed
description The perception–action account of empathy states that observation of another person's state automatically activates a similar state in the observer. It is still unclear in what way ongoing sensorimotor alpha oscillations are involved in this process. Although they have been repeatedly implicated in (biological) action observation and understanding communicative gestures, less is known about their role in vicarious pain observation. Their role is understood as providing a graded inhibition through functional inhibition, thereby streamlining information flow through the cortex. Although alpha oscillations have been shown to have at least visual and sensorimotor origins, only the latter are expected to be involved in the empathetic response. Here, we used magnetoencephalography, allowing us to spatially distinguish and localize oscillatory components using beamformer source reconstruction. Subjects observed realistic pictures of limbs in painful and no-pain (control) conditions. As predicted, time–frequency analysis indeed showed increased alpha suppression in the pain condition compared to the no-pain condition. Although both pain and no-pain conditions suppressed alpha- and beta-band activity at both posterior and central sensors, the pain condition suppressed alpha more only at central sensors. Source reconstruction localized these differences along the central sulcus. Our results could not be accounted for by differences in the evoked fields, suggesting a unique role of oscillatory activity in empathetic responses. We argue that alpha oscillations provide a unique measure of the underlying functional architecture of the brain, suggesting an automatic disinhibition of the sensorimotor cortices in response to the observation of pain in others.
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spelling pubmed-31888152011-10-17 Sensorimotor Alpha Activity is Modulated in Response to the Observation of Pain in Others Whitmarsh, Stephen Nieuwenhuis, Ingrid L. C. Barendregt, Henk P. Jensen, Ole Front Hum Neurosci Neuroscience The perception–action account of empathy states that observation of another person's state automatically activates a similar state in the observer. It is still unclear in what way ongoing sensorimotor alpha oscillations are involved in this process. Although they have been repeatedly implicated in (biological) action observation and understanding communicative gestures, less is known about their role in vicarious pain observation. Their role is understood as providing a graded inhibition through functional inhibition, thereby streamlining information flow through the cortex. Although alpha oscillations have been shown to have at least visual and sensorimotor origins, only the latter are expected to be involved in the empathetic response. Here, we used magnetoencephalography, allowing us to spatially distinguish and localize oscillatory components using beamformer source reconstruction. Subjects observed realistic pictures of limbs in painful and no-pain (control) conditions. As predicted, time–frequency analysis indeed showed increased alpha suppression in the pain condition compared to the no-pain condition. Although both pain and no-pain conditions suppressed alpha- and beta-band activity at both posterior and central sensors, the pain condition suppressed alpha more only at central sensors. Source reconstruction localized these differences along the central sulcus. Our results could not be accounted for by differences in the evoked fields, suggesting a unique role of oscillatory activity in empathetic responses. We argue that alpha oscillations provide a unique measure of the underlying functional architecture of the brain, suggesting an automatic disinhibition of the sensorimotor cortices in response to the observation of pain in others. Frontiers Research Foundation 2011-10-04 /pmc/articles/PMC3188815/ /pubmed/22007165 http://dx.doi.org/10.3389/fnhum.2011.00091 Text en Copyright © 2011 Whitmarsh, Nieuwenhuis, Barendregt and Jensen. http://www.frontiersin.org/licenseagreement This is an open-access article subject to a non-exclusive license between the authors and Frontiers Media SA, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and other Frontiers conditions are complied with.
spellingShingle Neuroscience
Whitmarsh, Stephen
Nieuwenhuis, Ingrid L. C.
Barendregt, Henk P.
Jensen, Ole
Sensorimotor Alpha Activity is Modulated in Response to the Observation of Pain in Others
title Sensorimotor Alpha Activity is Modulated in Response to the Observation of Pain in Others
title_full Sensorimotor Alpha Activity is Modulated in Response to the Observation of Pain in Others
title_fullStr Sensorimotor Alpha Activity is Modulated in Response to the Observation of Pain in Others
title_full_unstemmed Sensorimotor Alpha Activity is Modulated in Response to the Observation of Pain in Others
title_short Sensorimotor Alpha Activity is Modulated in Response to the Observation of Pain in Others
title_sort sensorimotor alpha activity is modulated in response to the observation of pain in others
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3188815/
https://www.ncbi.nlm.nih.gov/pubmed/22007165
http://dx.doi.org/10.3389/fnhum.2011.00091
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