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Neuropeptide Y-expressing dorsal horn inhibitory interneurons gate spinal pain and itch signalling

Somatosensory information is processed by a complex network of interneurons in the spinal dorsal horn. It has been reported that inhibitory interneurons that express neuropeptide Y (NPY), either permanently or during development, suppress mechanical itch, with no effect on pain. Here, we investigate...

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Autores principales: Boyle, Kieran A, Polgar, Erika, Gutierrez-Mecinas, Maria, Dickie, Allen C, Cooper, Andrew H, Bell, Andrew M, Jumolea, Evelline, Casas-Benito, Adrian, Watanabe, Masahiko, Hughes, David I, Weir, Gregory A, Riddell, John S, Todd, Andrew J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10392120/
https://www.ncbi.nlm.nih.gov/pubmed/37490401
http://dx.doi.org/10.7554/eLife.86633
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author Boyle, Kieran A
Polgar, Erika
Gutierrez-Mecinas, Maria
Dickie, Allen C
Cooper, Andrew H
Bell, Andrew M
Jumolea, Evelline
Casas-Benito, Adrian
Watanabe, Masahiko
Hughes, David I
Weir, Gregory A
Riddell, John S
Todd, Andrew J
author_facet Boyle, Kieran A
Polgar, Erika
Gutierrez-Mecinas, Maria
Dickie, Allen C
Cooper, Andrew H
Bell, Andrew M
Jumolea, Evelline
Casas-Benito, Adrian
Watanabe, Masahiko
Hughes, David I
Weir, Gregory A
Riddell, John S
Todd, Andrew J
author_sort Boyle, Kieran A
collection PubMed
description Somatosensory information is processed by a complex network of interneurons in the spinal dorsal horn. It has been reported that inhibitory interneurons that express neuropeptide Y (NPY), either permanently or during development, suppress mechanical itch, with no effect on pain. Here, we investigate the role of interneurons that continue to express NPY (NPY-INs) in the adult mouse spinal cord. We find that chemogenetic activation of NPY-INs reduces behaviours associated with acute pain and pruritogen-evoked itch, whereas silencing them causes exaggerated itch responses that depend on cells expressing the gastrin-releasing peptide receptor. As predicted by our previous studies, silencing of another population of inhibitory interneurons (those expressing dynorphin) also increases itch, but to a lesser extent. Importantly, NPY-IN activation also reduces behavioural signs of inflammatory and neuropathic pain. These results demonstrate that NPY-INs gate pain and itch transmission at the spinal level, and therefore represent a potential treatment target for pathological pain and itch.
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spelling pubmed-103921202023-08-02 Neuropeptide Y-expressing dorsal horn inhibitory interneurons gate spinal pain and itch signalling Boyle, Kieran A Polgar, Erika Gutierrez-Mecinas, Maria Dickie, Allen C Cooper, Andrew H Bell, Andrew M Jumolea, Evelline Casas-Benito, Adrian Watanabe, Masahiko Hughes, David I Weir, Gregory A Riddell, John S Todd, Andrew J eLife Neuroscience Somatosensory information is processed by a complex network of interneurons in the spinal dorsal horn. It has been reported that inhibitory interneurons that express neuropeptide Y (NPY), either permanently or during development, suppress mechanical itch, with no effect on pain. Here, we investigate the role of interneurons that continue to express NPY (NPY-INs) in the adult mouse spinal cord. We find that chemogenetic activation of NPY-INs reduces behaviours associated with acute pain and pruritogen-evoked itch, whereas silencing them causes exaggerated itch responses that depend on cells expressing the gastrin-releasing peptide receptor. As predicted by our previous studies, silencing of another population of inhibitory interneurons (those expressing dynorphin) also increases itch, but to a lesser extent. Importantly, NPY-IN activation also reduces behavioural signs of inflammatory and neuropathic pain. These results demonstrate that NPY-INs gate pain and itch transmission at the spinal level, and therefore represent a potential treatment target for pathological pain and itch. eLife Sciences Publications, Ltd 2023-07-25 /pmc/articles/PMC10392120/ /pubmed/37490401 http://dx.doi.org/10.7554/eLife.86633 Text en © 2023, Boyle, Polgar, Gutierrez-Mecinas et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Boyle, Kieran A
Polgar, Erika
Gutierrez-Mecinas, Maria
Dickie, Allen C
Cooper, Andrew H
Bell, Andrew M
Jumolea, Evelline
Casas-Benito, Adrian
Watanabe, Masahiko
Hughes, David I
Weir, Gregory A
Riddell, John S
Todd, Andrew J
Neuropeptide Y-expressing dorsal horn inhibitory interneurons gate spinal pain and itch signalling
title Neuropeptide Y-expressing dorsal horn inhibitory interneurons gate spinal pain and itch signalling
title_full Neuropeptide Y-expressing dorsal horn inhibitory interneurons gate spinal pain and itch signalling
title_fullStr Neuropeptide Y-expressing dorsal horn inhibitory interneurons gate spinal pain and itch signalling
title_full_unstemmed Neuropeptide Y-expressing dorsal horn inhibitory interneurons gate spinal pain and itch signalling
title_short Neuropeptide Y-expressing dorsal horn inhibitory interneurons gate spinal pain and itch signalling
title_sort neuropeptide y-expressing dorsal horn inhibitory interneurons gate spinal pain and itch signalling
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10392120/
https://www.ncbi.nlm.nih.gov/pubmed/37490401
http://dx.doi.org/10.7554/eLife.86633
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