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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2019
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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. |
format | Online Article Text |
id | pubmed-6709688 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
record_format | MEDLINE/PubMed |
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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