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Spinal Neuropeptide Y1 Receptor-Expressing Neurons Form an Essential Excitatory Pathway for Mechanical Itch

Acute itch can be generated by either chemical or mechanical stimuli, which activate separate pathways in the periphery and spinal cord. While substantial progress has been made in mapping the transmission pathway for chemical itch, the central pathway for mechanical itch remains obscure. Using comp...

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Autores principales: Acton, David, Ren, Xiangyu, Di Costanzo, Stefania, Dalet, Antoine, Bourane, Steeve, Bertocchi, Ilaria, Eva, Carola, Goulding, Martyn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709688/
https://www.ncbi.nlm.nih.gov/pubmed/31315043
http://dx.doi.org/10.1016/j.celrep.2019.06.033
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author Acton, David
Ren, Xiangyu
Di Costanzo, Stefania
Dalet, Antoine
Bourane, Steeve
Bertocchi, Ilaria
Eva, Carola
Goulding, Martyn
author_facet Acton, David
Ren, Xiangyu
Di Costanzo, Stefania
Dalet, Antoine
Bourane, Steeve
Bertocchi, Ilaria
Eva, Carola
Goulding, Martyn
author_sort Acton, David
collection PubMed
description Acute itch can be generated by either chemical or mechanical stimuli, which activate separate pathways in the periphery and spinal cord. While substantial progress has been made in mapping the transmission pathway for chemical itch, the central pathway for mechanical itch remains obscure. Using complementary genetic and pharmacological manipulations, we show that excitatory neurons marked by the expression of the neuropeptide Y1 receptor (Y1(Cre) neurons) form an essential pathway in the dorsal spinal cord for the transmission of mechanical but not chemical itch. Ablating or silencing the Y1(Cre) neurons abrogates mechanical itch, while chemogenetic activation induces scratching. Moreover, using Y1 conditional knockout mice, we demonstrate that endogenous neuropeptide Y (NPY) acts via dorsal horn Y1-expressing neurons to suppress light punctate touch and mechanical itch stimuli. NPY-Y1 signaling thus regulates the transmission of innocuous tactile information by establishing biologically relevant thresholds for touch discrimination and mechanical itch reflexes.
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spelling pubmed-67096882019-08-26 Spinal Neuropeptide Y1 Receptor-Expressing Neurons Form an Essential Excitatory Pathway for Mechanical Itch Acton, David Ren, Xiangyu Di Costanzo, Stefania Dalet, Antoine Bourane, Steeve Bertocchi, Ilaria Eva, Carola Goulding, Martyn Cell Rep Article Acute itch can be generated by either chemical or mechanical stimuli, which activate separate pathways in the periphery and spinal cord. While substantial progress has been made in mapping the transmission pathway for chemical itch, the central pathway for mechanical itch remains obscure. Using complementary genetic and pharmacological manipulations, we show that excitatory neurons marked by the expression of the neuropeptide Y1 receptor (Y1(Cre) neurons) form an essential pathway in the dorsal spinal cord for the transmission of mechanical but not chemical itch. Ablating or silencing the Y1(Cre) neurons abrogates mechanical itch, while chemogenetic activation induces scratching. Moreover, using Y1 conditional knockout mice, we demonstrate that endogenous neuropeptide Y (NPY) acts via dorsal horn Y1-expressing neurons to suppress light punctate touch and mechanical itch stimuli. NPY-Y1 signaling thus regulates the transmission of innocuous tactile information by establishing biologically relevant thresholds for touch discrimination and mechanical itch reflexes. 2019-07-16 /pmc/articles/PMC6709688/ /pubmed/31315043 http://dx.doi.org/10.1016/j.celrep.2019.06.033 Text en This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Acton, David
Ren, Xiangyu
Di Costanzo, Stefania
Dalet, Antoine
Bourane, Steeve
Bertocchi, Ilaria
Eva, Carola
Goulding, Martyn
Spinal Neuropeptide Y1 Receptor-Expressing Neurons Form an Essential Excitatory Pathway for Mechanical Itch
title Spinal Neuropeptide Y1 Receptor-Expressing Neurons Form an Essential Excitatory Pathway for Mechanical Itch
title_full Spinal Neuropeptide Y1 Receptor-Expressing Neurons Form an Essential Excitatory Pathway for Mechanical Itch
title_fullStr Spinal Neuropeptide Y1 Receptor-Expressing Neurons Form an Essential Excitatory Pathway for Mechanical Itch
title_full_unstemmed Spinal Neuropeptide Y1 Receptor-Expressing Neurons Form an Essential Excitatory Pathway for Mechanical Itch
title_short Spinal Neuropeptide Y1 Receptor-Expressing Neurons Form an Essential Excitatory Pathway for Mechanical Itch
title_sort spinal neuropeptide y1 receptor-expressing neurons form an essential excitatory pathway for mechanical itch
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709688/
https://www.ncbi.nlm.nih.gov/pubmed/31315043
http://dx.doi.org/10.1016/j.celrep.2019.06.033
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