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Cell type-specific modulation of sensory and affective components of itch in the periaqueductal gray
Itch is a distinct aversive sensation that elicits a strong urge to scratch. Despite recent advances in our understanding of the peripheral basis of itch, we know very little regarding how central neural circuits modulate acute and chronic itch processing. Here we establish the causal contributions...
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/PMC6761157/ https://www.ncbi.nlm.nih.gov/pubmed/31554789 http://dx.doi.org/10.1038/s41467-019-12316-0 |
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author | Samineni, Vijay K. Grajales-Reyes, Jose G. Sundaram, Saranya S. Yoo, Judy J. Gereau, Robert W. |
author_facet | Samineni, Vijay K. Grajales-Reyes, Jose G. Sundaram, Saranya S. Yoo, Judy J. Gereau, Robert W. |
author_sort | Samineni, Vijay K. |
collection | PubMed |
description | Itch is a distinct aversive sensation that elicits a strong urge to scratch. Despite recent advances in our understanding of the peripheral basis of itch, we know very little regarding how central neural circuits modulate acute and chronic itch processing. Here we establish the causal contributions of defined periaqueductal gray (PAG) neuronal populations in itch modulation in mice. Chemogenetic manipulations demonstrate bidirectional modulation of scratching by neurons in the PAG. Fiber photometry studies show that activity of GABAergic and glutamatergic neurons in the PAG is modulated in an opposing manner during chloroquine-evoked scratching. Furthermore, activation of PAG GABAergic neurons or inhibition of glutamatergic neurons resulted in attenuation of scratching in both acute and chronic pruritis. Surprisingly, PAG GABAergic neurons, but not glutamatergic neurons, may encode the aversive component of itch. Thus, the PAG represents a neuromodulatory hub that regulates both the sensory and affective aspects of acute and chronic itch. |
format | Online Article Text |
id | pubmed-6761157 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67611572019-09-27 Cell type-specific modulation of sensory and affective components of itch in the periaqueductal gray Samineni, Vijay K. Grajales-Reyes, Jose G. Sundaram, Saranya S. Yoo, Judy J. Gereau, Robert W. Nat Commun Article Itch is a distinct aversive sensation that elicits a strong urge to scratch. Despite recent advances in our understanding of the peripheral basis of itch, we know very little regarding how central neural circuits modulate acute and chronic itch processing. Here we establish the causal contributions of defined periaqueductal gray (PAG) neuronal populations in itch modulation in mice. Chemogenetic manipulations demonstrate bidirectional modulation of scratching by neurons in the PAG. Fiber photometry studies show that activity of GABAergic and glutamatergic neurons in the PAG is modulated in an opposing manner during chloroquine-evoked scratching. Furthermore, activation of PAG GABAergic neurons or inhibition of glutamatergic neurons resulted in attenuation of scratching in both acute and chronic pruritis. Surprisingly, PAG GABAergic neurons, but not glutamatergic neurons, may encode the aversive component of itch. Thus, the PAG represents a neuromodulatory hub that regulates both the sensory and affective aspects of acute and chronic itch. Nature Publishing Group UK 2019-09-25 /pmc/articles/PMC6761157/ /pubmed/31554789 http://dx.doi.org/10.1038/s41467-019-12316-0 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 Samineni, Vijay K. Grajales-Reyes, Jose G. Sundaram, Saranya S. Yoo, Judy J. Gereau, Robert W. Cell type-specific modulation of sensory and affective components of itch in the periaqueductal gray |
title | Cell type-specific modulation of sensory and affective components of itch in the periaqueductal gray |
title_full | Cell type-specific modulation of sensory and affective components of itch in the periaqueductal gray |
title_fullStr | Cell type-specific modulation of sensory and affective components of itch in the periaqueductal gray |
title_full_unstemmed | Cell type-specific modulation of sensory and affective components of itch in the periaqueductal gray |
title_short | Cell type-specific modulation of sensory and affective components of itch in the periaqueductal gray |
title_sort | cell type-specific modulation of sensory and affective components of itch in the periaqueductal gray |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6761157/ https://www.ncbi.nlm.nih.gov/pubmed/31554789 http://dx.doi.org/10.1038/s41467-019-12316-0 |
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