Cargando…

Central medial thalamic nucleus dynamically participates in acute itch sensation and chronic itch-induced anxiety-like behavior in male mice

Itch is an annoying sensation consisting of both sensory and emotional components. It is known to involve the parabrachial nucleus (PBN), but the following transmission nodes remain elusive. The present study identified that the PBN-central medial thalamic nucleus (CM)-medial prefrontal cortex (mPFC...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Jia-Ni, Wu, Xue-Mei, Zhao, Liu-Jie, Sun, Han-Xue, Hong, Jie, Wu, Feng-Ling, Chen, Si-Hai, Chen, Tao, Li, Hui, Dong, Yu-Lin, Li, Yun-Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10156671/
https://www.ncbi.nlm.nih.gov/pubmed/37137899
http://dx.doi.org/10.1038/s41467-023-38264-4
_version_ 1785036587864686592
author Li, Jia-Ni
Wu, Xue-Mei
Zhao, Liu-Jie
Sun, Han-Xue
Hong, Jie
Wu, Feng-Ling
Chen, Si-Hai
Chen, Tao
Li, Hui
Dong, Yu-Lin
Li, Yun-Qing
author_facet Li, Jia-Ni
Wu, Xue-Mei
Zhao, Liu-Jie
Sun, Han-Xue
Hong, Jie
Wu, Feng-Ling
Chen, Si-Hai
Chen, Tao
Li, Hui
Dong, Yu-Lin
Li, Yun-Qing
author_sort Li, Jia-Ni
collection PubMed
description Itch is an annoying sensation consisting of both sensory and emotional components. It is known to involve the parabrachial nucleus (PBN), but the following transmission nodes remain elusive. The present study identified that the PBN-central medial thalamic nucleus (CM)-medial prefrontal cortex (mPFC) pathway is essential for itch signal transmission at the supraspinal level in male mice. Chemogenetic inhibition of the CM-mPFC pathway attenuates scratching behavior or chronic itch-related affective responses. CM input to mPFC pyramidal neurons is enhanced in acute and chronic itch models. Specifically chronic itch stimuli also alter mPFC interneuron involvement, resulting in enhanced feedforward inhibition and a distorted excitatory/inhibitory balance in mPFC pyramidal neurons. The present work underscores CM as a transmit node of the itch signal in the thalamus, which is dynamically engaged in both the sensory and affective dimensions of itch with different stimulus salience.
format Online
Article
Text
id pubmed-10156671
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-101566712023-05-05 Central medial thalamic nucleus dynamically participates in acute itch sensation and chronic itch-induced anxiety-like behavior in male mice Li, Jia-Ni Wu, Xue-Mei Zhao, Liu-Jie Sun, Han-Xue Hong, Jie Wu, Feng-Ling Chen, Si-Hai Chen, Tao Li, Hui Dong, Yu-Lin Li, Yun-Qing Nat Commun Article Itch is an annoying sensation consisting of both sensory and emotional components. It is known to involve the parabrachial nucleus (PBN), but the following transmission nodes remain elusive. The present study identified that the PBN-central medial thalamic nucleus (CM)-medial prefrontal cortex (mPFC) pathway is essential for itch signal transmission at the supraspinal level in male mice. Chemogenetic inhibition of the CM-mPFC pathway attenuates scratching behavior or chronic itch-related affective responses. CM input to mPFC pyramidal neurons is enhanced in acute and chronic itch models. Specifically chronic itch stimuli also alter mPFC interneuron involvement, resulting in enhanced feedforward inhibition and a distorted excitatory/inhibitory balance in mPFC pyramidal neurons. The present work underscores CM as a transmit node of the itch signal in the thalamus, which is dynamically engaged in both the sensory and affective dimensions of itch with different stimulus salience. Nature Publishing Group UK 2023-05-03 /pmc/articles/PMC10156671/ /pubmed/37137899 http://dx.doi.org/10.1038/s41467-023-38264-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Li, Jia-Ni
Wu, Xue-Mei
Zhao, Liu-Jie
Sun, Han-Xue
Hong, Jie
Wu, Feng-Ling
Chen, Si-Hai
Chen, Tao
Li, Hui
Dong, Yu-Lin
Li, Yun-Qing
Central medial thalamic nucleus dynamically participates in acute itch sensation and chronic itch-induced anxiety-like behavior in male mice
title Central medial thalamic nucleus dynamically participates in acute itch sensation and chronic itch-induced anxiety-like behavior in male mice
title_full Central medial thalamic nucleus dynamically participates in acute itch sensation and chronic itch-induced anxiety-like behavior in male mice
title_fullStr Central medial thalamic nucleus dynamically participates in acute itch sensation and chronic itch-induced anxiety-like behavior in male mice
title_full_unstemmed Central medial thalamic nucleus dynamically participates in acute itch sensation and chronic itch-induced anxiety-like behavior in male mice
title_short Central medial thalamic nucleus dynamically participates in acute itch sensation and chronic itch-induced anxiety-like behavior in male mice
title_sort central medial thalamic nucleus dynamically participates in acute itch sensation and chronic itch-induced anxiety-like behavior in male mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10156671/
https://www.ncbi.nlm.nih.gov/pubmed/37137899
http://dx.doi.org/10.1038/s41467-023-38264-4
work_keys_str_mv AT lijiani centralmedialthalamicnucleusdynamicallyparticipatesinacuteitchsensationandchronicitchinducedanxietylikebehaviorinmalemice
AT wuxuemei centralmedialthalamicnucleusdynamicallyparticipatesinacuteitchsensationandchronicitchinducedanxietylikebehaviorinmalemice
AT zhaoliujie centralmedialthalamicnucleusdynamicallyparticipatesinacuteitchsensationandchronicitchinducedanxietylikebehaviorinmalemice
AT sunhanxue centralmedialthalamicnucleusdynamicallyparticipatesinacuteitchsensationandchronicitchinducedanxietylikebehaviorinmalemice
AT hongjie centralmedialthalamicnucleusdynamicallyparticipatesinacuteitchsensationandchronicitchinducedanxietylikebehaviorinmalemice
AT wufengling centralmedialthalamicnucleusdynamicallyparticipatesinacuteitchsensationandchronicitchinducedanxietylikebehaviorinmalemice
AT chensihai centralmedialthalamicnucleusdynamicallyparticipatesinacuteitchsensationandchronicitchinducedanxietylikebehaviorinmalemice
AT chentao centralmedialthalamicnucleusdynamicallyparticipatesinacuteitchsensationandchronicitchinducedanxietylikebehaviorinmalemice
AT lihui centralmedialthalamicnucleusdynamicallyparticipatesinacuteitchsensationandchronicitchinducedanxietylikebehaviorinmalemice
AT dongyulin centralmedialthalamicnucleusdynamicallyparticipatesinacuteitchsensationandchronicitchinducedanxietylikebehaviorinmalemice
AT liyunqing centralmedialthalamicnucleusdynamicallyparticipatesinacuteitchsensationandchronicitchinducedanxietylikebehaviorinmalemice