Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Samineni, Vijay K., Grajales-Reyes, Jose G., Sundaram, Saranya S., Yoo, Judy J., Gereau, Robert W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
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
_version_ 1783453966797897728
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
work_keys_str_mv AT saminenivijayk celltypespecificmodulationofsensoryandaffectivecomponentsofitchintheperiaqueductalgray
AT grajalesreyesjoseg celltypespecificmodulationofsensoryandaffectivecomponentsofitchintheperiaqueductalgray
AT sundaramsaranyas celltypespecificmodulationofsensoryandaffectivecomponentsofitchintheperiaqueductalgray
AT yoojudyj celltypespecificmodulationofsensoryandaffectivecomponentsofitchintheperiaqueductalgray
AT gereaurobertw celltypespecificmodulationofsensoryandaffectivecomponentsofitchintheperiaqueductalgray