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The Neural Origin of Nociceptive-Induced Gamma-Band Oscillations

Gamma-band oscillations (GBOs) elicited by transient nociceptive stimuli are one of the most promising biomarkers of pain across species. Still, whether these GBOs reflect stimulus encoding in the primary somatosensory cortex (S1) or nocifensive behavior in the primary motor cortex (M1) is debated....

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Detalles Bibliográficos
Autores principales: Yue, Lupeng, Iannetti, G.D., Hu, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7178916/
https://www.ncbi.nlm.nih.gov/pubmed/32241836
http://dx.doi.org/10.1523/JNEUROSCI.0255-20.2020
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author Yue, Lupeng
Iannetti, G.D.
Hu, Li
author_facet Yue, Lupeng
Iannetti, G.D.
Hu, Li
author_sort Yue, Lupeng
collection PubMed
description Gamma-band oscillations (GBOs) elicited by transient nociceptive stimuli are one of the most promising biomarkers of pain across species. Still, whether these GBOs reflect stimulus encoding in the primary somatosensory cortex (S1) or nocifensive behavior in the primary motor cortex (M1) is debated. Here we recorded neural activity simultaneously from the brain surface as well as at different depths of the bilateral S1/M1 in freely-moving male rats receiving nociceptive stimulation. GBOs measured from superficial layers of S1 contralateral to the stimulated paw not only had the largest magnitude, but also showed the strongest temporal and phase coupling with epidural GBOs. Also, spiking of superficial S1 interneurons had the strongest phase coherence with epidural GBOs. These results provide the first direct demonstration that scalp GBOs, one of the most promising pain biomarkers, reflect neural activity strongly coupled with the fast spiking of interneurons in the superficial layers of the S1 contralateral to the stimulated side. SIGNIFICANCE STATEMENT Nociceptive-induced gamma-band oscillations (GBOs) measured at population level are one of the most promising biomarkers of pain perception. Our results provide the direct demonstration that these GBOs reflect neural activity coupled with the spike firing of interneurons in the superficial layers of the primary somatosensory cortex (S1) contralateral to the side of nociceptive stimulation. These results address the ongoing debate about whether nociceptive-induced GBOs recorded with scalp EEG or epidurally reflect stimulus encoding in the S1 or nocifensive behavior in the primary motor cortex (M1), and will therefore influence how experiments in pain neuroscience will be designed and interpreted.
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spelling pubmed-71789162020-05-29 The Neural Origin of Nociceptive-Induced Gamma-Band Oscillations Yue, Lupeng Iannetti, G.D. Hu, Li J Neurosci Research Articles Gamma-band oscillations (GBOs) elicited by transient nociceptive stimuli are one of the most promising biomarkers of pain across species. Still, whether these GBOs reflect stimulus encoding in the primary somatosensory cortex (S1) or nocifensive behavior in the primary motor cortex (M1) is debated. Here we recorded neural activity simultaneously from the brain surface as well as at different depths of the bilateral S1/M1 in freely-moving male rats receiving nociceptive stimulation. GBOs measured from superficial layers of S1 contralateral to the stimulated paw not only had the largest magnitude, but also showed the strongest temporal and phase coupling with epidural GBOs. Also, spiking of superficial S1 interneurons had the strongest phase coherence with epidural GBOs. These results provide the first direct demonstration that scalp GBOs, one of the most promising pain biomarkers, reflect neural activity strongly coupled with the fast spiking of interneurons in the superficial layers of the S1 contralateral to the stimulated side. SIGNIFICANCE STATEMENT Nociceptive-induced gamma-band oscillations (GBOs) measured at population level are one of the most promising biomarkers of pain perception. Our results provide the direct demonstration that these GBOs reflect neural activity coupled with the spike firing of interneurons in the superficial layers of the primary somatosensory cortex (S1) contralateral to the side of nociceptive stimulation. These results address the ongoing debate about whether nociceptive-induced GBOs recorded with scalp EEG or epidurally reflect stimulus encoding in the S1 or nocifensive behavior in the primary motor cortex (M1), and will therefore influence how experiments in pain neuroscience will be designed and interpreted. Society for Neuroscience 2020-04-22 /pmc/articles/PMC7178916/ /pubmed/32241836 http://dx.doi.org/10.1523/JNEUROSCI.0255-20.2020 Text en Copyright © 2020 Yue et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License Creative Commons Attribution 4.0 International (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Articles
Yue, Lupeng
Iannetti, G.D.
Hu, Li
The Neural Origin of Nociceptive-Induced Gamma-Band Oscillations
title The Neural Origin of Nociceptive-Induced Gamma-Band Oscillations
title_full The Neural Origin of Nociceptive-Induced Gamma-Band Oscillations
title_fullStr The Neural Origin of Nociceptive-Induced Gamma-Band Oscillations
title_full_unstemmed The Neural Origin of Nociceptive-Induced Gamma-Band Oscillations
title_short The Neural Origin of Nociceptive-Induced Gamma-Band Oscillations
title_sort neural origin of nociceptive-induced gamma-band oscillations
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7178916/
https://www.ncbi.nlm.nih.gov/pubmed/32241836
http://dx.doi.org/10.1523/JNEUROSCI.0255-20.2020
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