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Parvalbumin Neurons in Zona Incerta Regulate Itch in Mice
Pain and itch are intricately entangled at both circuitry and behavioral levels. Emerging evidence indicates that parvalbumin (PV)-expressing neurons in zona incerta (ZI) are critical for promoting nocifensive behaviors. However, the role of these neurons in itch modulation remains elusive. Herein,...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8920991/ https://www.ncbi.nlm.nih.gov/pubmed/35299695 http://dx.doi.org/10.3389/fnmol.2022.843754 |
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author | Li, Jiaqi Bai, Yang Liang, Yi Zhang, Yiwen Zhao, Qiuying Ge, Junye Li, Dangchao Zhu, Yuanyuan Cai, Guohong Tao, Huiren Wu, Shengxi Huang, Jing |
author_facet | Li, Jiaqi Bai, Yang Liang, Yi Zhang, Yiwen Zhao, Qiuying Ge, Junye Li, Dangchao Zhu, Yuanyuan Cai, Guohong Tao, Huiren Wu, Shengxi Huang, Jing |
author_sort | Li, Jiaqi |
collection | PubMed |
description | Pain and itch are intricately entangled at both circuitry and behavioral levels. Emerging evidence indicates that parvalbumin (PV)-expressing neurons in zona incerta (ZI) are critical for promoting nocifensive behaviors. However, the role of these neurons in itch modulation remains elusive. Herein, by combining FOS immunostaining, fiber photometry, and chemogenetic manipulation, we reveal that ZI PV neurons act as an endogenous negative diencephalic modulator for itch processing. Morphological data showed that both histamine and chloroquine stimuli induced FOS expression in ZI PV neurons. The activation of these neurons was further supported by the increased calcium signal upon scratching behavior evoked by acute itch. Behavioral data further indicated that chemogenetic activation of these neurons reduced scratching behaviors related to histaminergic and non-histaminergic acute itch. Similar neural activity and modulatory role of ZI PV neurons were seen in mice with chronic itch induced by atopic dermatitis. Together, our study provides direct evidence for the role of ZI PV neurons in regulating itch, and identifies a potential target for the remedy of chronic itch. |
format | Online Article Text |
id | pubmed-8920991 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-89209912022-03-16 Parvalbumin Neurons in Zona Incerta Regulate Itch in Mice Li, Jiaqi Bai, Yang Liang, Yi Zhang, Yiwen Zhao, Qiuying Ge, Junye Li, Dangchao Zhu, Yuanyuan Cai, Guohong Tao, Huiren Wu, Shengxi Huang, Jing Front Mol Neurosci Molecular Neuroscience Pain and itch are intricately entangled at both circuitry and behavioral levels. Emerging evidence indicates that parvalbumin (PV)-expressing neurons in zona incerta (ZI) are critical for promoting nocifensive behaviors. However, the role of these neurons in itch modulation remains elusive. Herein, by combining FOS immunostaining, fiber photometry, and chemogenetic manipulation, we reveal that ZI PV neurons act as an endogenous negative diencephalic modulator for itch processing. Morphological data showed that both histamine and chloroquine stimuli induced FOS expression in ZI PV neurons. The activation of these neurons was further supported by the increased calcium signal upon scratching behavior evoked by acute itch. Behavioral data further indicated that chemogenetic activation of these neurons reduced scratching behaviors related to histaminergic and non-histaminergic acute itch. Similar neural activity and modulatory role of ZI PV neurons were seen in mice with chronic itch induced by atopic dermatitis. Together, our study provides direct evidence for the role of ZI PV neurons in regulating itch, and identifies a potential target for the remedy of chronic itch. Frontiers Media S.A. 2022-03-01 /pmc/articles/PMC8920991/ /pubmed/35299695 http://dx.doi.org/10.3389/fnmol.2022.843754 Text en Copyright © 2022 Li, Bai, Liang, Zhang, Zhao, Ge, Li, Zhu, Cai, Tao, Wu and Huang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Molecular Neuroscience Li, Jiaqi Bai, Yang Liang, Yi Zhang, Yiwen Zhao, Qiuying Ge, Junye Li, Dangchao Zhu, Yuanyuan Cai, Guohong Tao, Huiren Wu, Shengxi Huang, Jing Parvalbumin Neurons in Zona Incerta Regulate Itch in Mice |
title | Parvalbumin Neurons in Zona Incerta Regulate Itch in Mice |
title_full | Parvalbumin Neurons in Zona Incerta Regulate Itch in Mice |
title_fullStr | Parvalbumin Neurons in Zona Incerta Regulate Itch in Mice |
title_full_unstemmed | Parvalbumin Neurons in Zona Incerta Regulate Itch in Mice |
title_short | Parvalbumin Neurons in Zona Incerta Regulate Itch in Mice |
title_sort | parvalbumin neurons in zona incerta regulate itch in mice |
topic | Molecular Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8920991/ https://www.ncbi.nlm.nih.gov/pubmed/35299695 http://dx.doi.org/10.3389/fnmol.2022.843754 |
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