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Gamma oscillations in somatosensory cortex recruit prefrontal and descending serotonergic pathways in aversion and nociception
In humans, gamma-band oscillations in the primary somatosensory cortex (S1) correlate with subjective pain perception. However, functional contributions to pain and the nature of underlying circuits are unclear. Here we report that gamma oscillations, but not other rhythms, are specifically strength...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6395755/ https://www.ncbi.nlm.nih.gov/pubmed/30816113 http://dx.doi.org/10.1038/s41467-019-08873-z |
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author | Tan, Linette Liqi Oswald, Manfred Josef Heinl, Céline Retana Romero, Oscar Andrés Kaushalya, Sanjeev Kumar Monyer, Hannah Kuner, Rohini |
author_facet | Tan, Linette Liqi Oswald, Manfred Josef Heinl, Céline Retana Romero, Oscar Andrés Kaushalya, Sanjeev Kumar Monyer, Hannah Kuner, Rohini |
author_sort | Tan, Linette Liqi |
collection | PubMed |
description | In humans, gamma-band oscillations in the primary somatosensory cortex (S1) correlate with subjective pain perception. However, functional contributions to pain and the nature of underlying circuits are unclear. Here we report that gamma oscillations, but not other rhythms, are specifically strengthened independently of any motor component in the S1 cortex of mice during nociception. Moreover, mice with inflammatory pain show elevated resting gamma and alpha activity and increased gamma power in response to sub-threshold stimuli, in association with behavioral nociceptive hypersensitivity. Inducing gamma oscillations via optogenetic activation of parvalbumin-expressing inhibitory interneurons in the S1 cortex enhances nociceptive sensitivity and induces aversive avoidance behavior. Activity mapping identified a network of prefrontal cortical and subcortical centers whilst morphological tracing and pharmacological studies demonstrate the requirement of descending serotonergic facilitatory pathways in these pain-related behaviors. This study thus describes a mechanistic framework for modulation of pain by specific activity patterns in the S1 cortex. |
format | Online Article Text |
id | pubmed-6395755 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63957552019-03-04 Gamma oscillations in somatosensory cortex recruit prefrontal and descending serotonergic pathways in aversion and nociception Tan, Linette Liqi Oswald, Manfred Josef Heinl, Céline Retana Romero, Oscar Andrés Kaushalya, Sanjeev Kumar Monyer, Hannah Kuner, Rohini Nat Commun Article In humans, gamma-band oscillations in the primary somatosensory cortex (S1) correlate with subjective pain perception. However, functional contributions to pain and the nature of underlying circuits are unclear. Here we report that gamma oscillations, but not other rhythms, are specifically strengthened independently of any motor component in the S1 cortex of mice during nociception. Moreover, mice with inflammatory pain show elevated resting gamma and alpha activity and increased gamma power in response to sub-threshold stimuli, in association with behavioral nociceptive hypersensitivity. Inducing gamma oscillations via optogenetic activation of parvalbumin-expressing inhibitory interneurons in the S1 cortex enhances nociceptive sensitivity and induces aversive avoidance behavior. Activity mapping identified a network of prefrontal cortical and subcortical centers whilst morphological tracing and pharmacological studies demonstrate the requirement of descending serotonergic facilitatory pathways in these pain-related behaviors. This study thus describes a mechanistic framework for modulation of pain by specific activity patterns in the S1 cortex. Nature Publishing Group UK 2019-02-28 /pmc/articles/PMC6395755/ /pubmed/30816113 http://dx.doi.org/10.1038/s41467-019-08873-z Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Tan, Linette Liqi Oswald, Manfred Josef Heinl, Céline Retana Romero, Oscar Andrés Kaushalya, Sanjeev Kumar Monyer, Hannah Kuner, Rohini Gamma oscillations in somatosensory cortex recruit prefrontal and descending serotonergic pathways in aversion and nociception |
title | Gamma oscillations in somatosensory cortex recruit prefrontal and descending serotonergic pathways in aversion and nociception |
title_full | Gamma oscillations in somatosensory cortex recruit prefrontal and descending serotonergic pathways in aversion and nociception |
title_fullStr | Gamma oscillations in somatosensory cortex recruit prefrontal and descending serotonergic pathways in aversion and nociception |
title_full_unstemmed | Gamma oscillations in somatosensory cortex recruit prefrontal and descending serotonergic pathways in aversion and nociception |
title_short | Gamma oscillations in somatosensory cortex recruit prefrontal and descending serotonergic pathways in aversion and nociception |
title_sort | gamma oscillations in somatosensory cortex recruit prefrontal and descending serotonergic pathways in aversion and nociception |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6395755/ https://www.ncbi.nlm.nih.gov/pubmed/30816113 http://dx.doi.org/10.1038/s41467-019-08873-z |
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