Nociceptive Local Field Potentials Recorded from the Human Insula Are Not Specific for Nociception.

The insula, particularly its posterior portion, is often regarded as a primary cortex for pain. However, this interpretation is largely based on reverse inference, and a specific involvement of the insula in pain has never been demonstrated. Taking advantage of the high spatiotemporal resolution of...

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Main Authors: Giulia Liberati, Anne Klöcker, Marta M Safronova, Susana Ferrão Santos, Jose-Geraldo Ribeiro Vaz, Christian Raftopoulos, André Mouraux
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-01-01
Series:PLoS Biology
Online Access:https://doi.org/10.1371/journal.pbio.1002345
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spelling doaj-9612f055878f40eea42687ec0bcd77c62021-07-02T17:09:05ZengPublic Library of Science (PLoS)PLoS Biology1544-91731545-78852016-01-01141e100234510.1371/journal.pbio.1002345Nociceptive Local Field Potentials Recorded from the Human Insula Are Not Specific for Nociception.Giulia LiberatiAnne KlöckerMarta M SafronovaSusana Ferrão SantosJose-Geraldo Ribeiro VazChristian RaftopoulosAndré MourauxThe insula, particularly its posterior portion, is often regarded as a primary cortex for pain. However, this interpretation is largely based on reverse inference, and a specific involvement of the insula in pain has never been demonstrated. Taking advantage of the high spatiotemporal resolution of direct intracerebral recordings, we investigated whether the human insula exhibits local field potentials (LFPs) specific for pain. Forty-seven insular sites were investigated. Participants received brief stimuli belonging to four different modalities (nociceptive, vibrotactile, auditory, and visual). Both nociceptive stimuli and non-nociceptive vibrotactile, auditory, and visual stimuli elicited consistent LFPs in the posterior and anterior insula, with matching spatial distributions. Furthermore, a blind source separation procedure showed that nociceptive LFPs are largely explained by multimodal neural activity also contributing to non-nociceptive LFPs. By revealing that LFPs elicited by nociceptive stimuli reflect activity unrelated to nociception and pain, our results confute the widespread assumption that these brain responses are a signature for pain perception and its modulation.https://doi.org/10.1371/journal.pbio.1002345
collection DOAJ
language English
format Article
sources DOAJ
author Giulia Liberati
Anne Klöcker
Marta M Safronova
Susana Ferrão Santos
Jose-Geraldo Ribeiro Vaz
Christian Raftopoulos
André Mouraux
spellingShingle Giulia Liberati
Anne Klöcker
Marta M Safronova
Susana Ferrão Santos
Jose-Geraldo Ribeiro Vaz
Christian Raftopoulos
André Mouraux
Nociceptive Local Field Potentials Recorded from the Human Insula Are Not Specific for Nociception.
PLoS Biology
author_facet Giulia Liberati
Anne Klöcker
Marta M Safronova
Susana Ferrão Santos
Jose-Geraldo Ribeiro Vaz
Christian Raftopoulos
André Mouraux
author_sort Giulia Liberati
title Nociceptive Local Field Potentials Recorded from the Human Insula Are Not Specific for Nociception.
title_short Nociceptive Local Field Potentials Recorded from the Human Insula Are Not Specific for Nociception.
title_full Nociceptive Local Field Potentials Recorded from the Human Insula Are Not Specific for Nociception.
title_fullStr Nociceptive Local Field Potentials Recorded from the Human Insula Are Not Specific for Nociception.
title_full_unstemmed Nociceptive Local Field Potentials Recorded from the Human Insula Are Not Specific for Nociception.
title_sort nociceptive local field potentials recorded from the human insula are not specific for nociception.
publisher Public Library of Science (PLoS)
series PLoS Biology
issn 1544-9173
1545-7885
publishDate 2016-01-01
description The insula, particularly its posterior portion, is often regarded as a primary cortex for pain. However, this interpretation is largely based on reverse inference, and a specific involvement of the insula in pain has never been demonstrated. Taking advantage of the high spatiotemporal resolution of direct intracerebral recordings, we investigated whether the human insula exhibits local field potentials (LFPs) specific for pain. Forty-seven insular sites were investigated. Participants received brief stimuli belonging to four different modalities (nociceptive, vibrotactile, auditory, and visual). Both nociceptive stimuli and non-nociceptive vibrotactile, auditory, and visual stimuli elicited consistent LFPs in the posterior and anterior insula, with matching spatial distributions. Furthermore, a blind source separation procedure showed that nociceptive LFPs are largely explained by multimodal neural activity also contributing to non-nociceptive LFPs. By revealing that LFPs elicited by nociceptive stimuli reflect activity unrelated to nociception and pain, our results confute the widespread assumption that these brain responses are a signature for pain perception and its modulation.
url https://doi.org/10.1371/journal.pbio.1002345
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