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Cholinergic basal forebrain nucleus of Meynert regulates chronic pain-like behavior via modulation of the prelimbic cortex
The basal nucleus of Meynert (NBM) subserves critically important functions in attention, arousal and cognition via its profound modulation of neocortical activity and is emerging as a key target in Alzheimer’s and Parkinson’s dementias. Despite the crucial role of neocortical domains in pain percep...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9411538/ https://www.ncbi.nlm.nih.gov/pubmed/36008394 http://dx.doi.org/10.1038/s41467-022-32558-9 |
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author | Oswald, Manfred J. Han, Yechao Li, Han Marashli, Samuel Oglo, Deniz Nouri Ojha, Bhavya Naser, Paul V. Gan, Zheng Kuner, Rohini |
author_facet | Oswald, Manfred J. Han, Yechao Li, Han Marashli, Samuel Oglo, Deniz Nouri Ojha, Bhavya Naser, Paul V. Gan, Zheng Kuner, Rohini |
author_sort | Oswald, Manfred J. |
collection | PubMed |
description | The basal nucleus of Meynert (NBM) subserves critically important functions in attention, arousal and cognition via its profound modulation of neocortical activity and is emerging as a key target in Alzheimer’s and Parkinson’s dementias. Despite the crucial role of neocortical domains in pain perception, however, the NBM has not been studied in models of chronic pain. Here, using in vivo tetrode recordings in behaving mice, we report that beta and gamma oscillatory activity is evoked in the NBM by noxious stimuli and is facilitated at peak inflammatory pain-like behavior. Optogenetic and chemogenetic cell-specific, reversible manipulations of NBM cholinergic-GABAergic neurons reveal their role in endogenous control of nociceptive hypersensitivity, which are manifest via projections to the prelimbic cortex, resulting in layer 5-mediated antinociception. Our data unravel the importance of the NBM in top-down control of neocortical processing of pain-like behavior. |
format | Online Article Text |
id | pubmed-9411538 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-94115382022-08-27 Cholinergic basal forebrain nucleus of Meynert regulates chronic pain-like behavior via modulation of the prelimbic cortex Oswald, Manfred J. Han, Yechao Li, Han Marashli, Samuel Oglo, Deniz Nouri Ojha, Bhavya Naser, Paul V. Gan, Zheng Kuner, Rohini Nat Commun Article The basal nucleus of Meynert (NBM) subserves critically important functions in attention, arousal and cognition via its profound modulation of neocortical activity and is emerging as a key target in Alzheimer’s and Parkinson’s dementias. Despite the crucial role of neocortical domains in pain perception, however, the NBM has not been studied in models of chronic pain. Here, using in vivo tetrode recordings in behaving mice, we report that beta and gamma oscillatory activity is evoked in the NBM by noxious stimuli and is facilitated at peak inflammatory pain-like behavior. Optogenetic and chemogenetic cell-specific, reversible manipulations of NBM cholinergic-GABAergic neurons reveal their role in endogenous control of nociceptive hypersensitivity, which are manifest via projections to the prelimbic cortex, resulting in layer 5-mediated antinociception. Our data unravel the importance of the NBM in top-down control of neocortical processing of pain-like behavior. Nature Publishing Group UK 2022-08-25 /pmc/articles/PMC9411538/ /pubmed/36008394 http://dx.doi.org/10.1038/s41467-022-32558-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Oswald, Manfred J. Han, Yechao Li, Han Marashli, Samuel Oglo, Deniz Nouri Ojha, Bhavya Naser, Paul V. Gan, Zheng Kuner, Rohini Cholinergic basal forebrain nucleus of Meynert regulates chronic pain-like behavior via modulation of the prelimbic cortex |
title | Cholinergic basal forebrain nucleus of Meynert regulates chronic pain-like behavior via modulation of the prelimbic cortex |
title_full | Cholinergic basal forebrain nucleus of Meynert regulates chronic pain-like behavior via modulation of the prelimbic cortex |
title_fullStr | Cholinergic basal forebrain nucleus of Meynert regulates chronic pain-like behavior via modulation of the prelimbic cortex |
title_full_unstemmed | Cholinergic basal forebrain nucleus of Meynert regulates chronic pain-like behavior via modulation of the prelimbic cortex |
title_short | Cholinergic basal forebrain nucleus of Meynert regulates chronic pain-like behavior via modulation of the prelimbic cortex |
title_sort | cholinergic basal forebrain nucleus of meynert regulates chronic pain-like behavior via modulation of the prelimbic cortex |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9411538/ https://www.ncbi.nlm.nih.gov/pubmed/36008394 http://dx.doi.org/10.1038/s41467-022-32558-9 |
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