Cargando…

A common neuronal ensemble in nucleus accumbens regulates pain-like behaviour and sleep

A comorbidity of chronic pain is sleep disturbance. Here, we identify a dual-functional ensemble that regulates both pain-like behaviour induced by chronic constrictive injury or complete Freund’s adjuvant, and sleep wakefulness, in the nucleus accumbens (NAc) in mice. Specifically, a select populat...

Descripción completa

Detalles Bibliográficos
Autores principales: Sun, Haiyan, Li, Zhilin, Qiu, Zhentong, Shen, Yu, Guo, Qingchen, Hu, Su-Wan, Ding, Hai-Lei, An, Shuming, Cao, Jun-Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10404280/
https://www.ncbi.nlm.nih.gov/pubmed/37543693
http://dx.doi.org/10.1038/s41467-023-40450-3
_version_ 1785085264410968064
author Sun, Haiyan
Li, Zhilin
Qiu, Zhentong
Shen, Yu
Guo, Qingchen
Hu, Su-Wan
Ding, Hai-Lei
An, Shuming
Cao, Jun-Li
author_facet Sun, Haiyan
Li, Zhilin
Qiu, Zhentong
Shen, Yu
Guo, Qingchen
Hu, Su-Wan
Ding, Hai-Lei
An, Shuming
Cao, Jun-Li
author_sort Sun, Haiyan
collection PubMed
description A comorbidity of chronic pain is sleep disturbance. Here, we identify a dual-functional ensemble that regulates both pain-like behaviour induced by chronic constrictive injury or complete Freund’s adjuvant, and sleep wakefulness, in the nucleus accumbens (NAc) in mice. Specifically, a select population of NAc neurons exhibits increased activity either upon nociceptive stimulation or during wakefulness. Experimental activation of the ensemble neurons exacerbates pain-like (nociceptive) responses and reduces NREM sleep, while inactivation of these neurons produces the opposite effects. Furthermore, NAc ensemble primarily consists of D1 neurons and projects divergently to the ventral tegmental area (VTA) and preoptic area (POA). Silencing an ensemble innervating VTA neurons selectively increases nociceptive responses without affecting sleep, whereas inhibiting ensemble-innervating POA neurons decreases NREM sleep without affecting nociception. These results suggest a common NAc ensemble that encodes chronic pain and controls sleep, and achieves the modality specificity through its divergent downstream circuit targets.
format Online
Article
Text
id pubmed-10404280
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-104042802023-08-07 A common neuronal ensemble in nucleus accumbens regulates pain-like behaviour and sleep Sun, Haiyan Li, Zhilin Qiu, Zhentong Shen, Yu Guo, Qingchen Hu, Su-Wan Ding, Hai-Lei An, Shuming Cao, Jun-Li Nat Commun Article A comorbidity of chronic pain is sleep disturbance. Here, we identify a dual-functional ensemble that regulates both pain-like behaviour induced by chronic constrictive injury or complete Freund’s adjuvant, and sleep wakefulness, in the nucleus accumbens (NAc) in mice. Specifically, a select population of NAc neurons exhibits increased activity either upon nociceptive stimulation or during wakefulness. Experimental activation of the ensemble neurons exacerbates pain-like (nociceptive) responses and reduces NREM sleep, while inactivation of these neurons produces the opposite effects. Furthermore, NAc ensemble primarily consists of D1 neurons and projects divergently to the ventral tegmental area (VTA) and preoptic area (POA). Silencing an ensemble innervating VTA neurons selectively increases nociceptive responses without affecting sleep, whereas inhibiting ensemble-innervating POA neurons decreases NREM sleep without affecting nociception. These results suggest a common NAc ensemble that encodes chronic pain and controls sleep, and achieves the modality specificity through its divergent downstream circuit targets. Nature Publishing Group UK 2023-08-05 /pmc/articles/PMC10404280/ /pubmed/37543693 http://dx.doi.org/10.1038/s41467-023-40450-3 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
Sun, Haiyan
Li, Zhilin
Qiu, Zhentong
Shen, Yu
Guo, Qingchen
Hu, Su-Wan
Ding, Hai-Lei
An, Shuming
Cao, Jun-Li
A common neuronal ensemble in nucleus accumbens regulates pain-like behaviour and sleep
title A common neuronal ensemble in nucleus accumbens regulates pain-like behaviour and sleep
title_full A common neuronal ensemble in nucleus accumbens regulates pain-like behaviour and sleep
title_fullStr A common neuronal ensemble in nucleus accumbens regulates pain-like behaviour and sleep
title_full_unstemmed A common neuronal ensemble in nucleus accumbens regulates pain-like behaviour and sleep
title_short A common neuronal ensemble in nucleus accumbens regulates pain-like behaviour and sleep
title_sort common neuronal ensemble in nucleus accumbens regulates pain-like behaviour and sleep
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10404280/
https://www.ncbi.nlm.nih.gov/pubmed/37543693
http://dx.doi.org/10.1038/s41467-023-40450-3
work_keys_str_mv AT sunhaiyan acommonneuronalensembleinnucleusaccumbensregulatespainlikebehaviourandsleep
AT lizhilin acommonneuronalensembleinnucleusaccumbensregulatespainlikebehaviourandsleep
AT qiuzhentong acommonneuronalensembleinnucleusaccumbensregulatespainlikebehaviourandsleep
AT shenyu acommonneuronalensembleinnucleusaccumbensregulatespainlikebehaviourandsleep
AT guoqingchen acommonneuronalensembleinnucleusaccumbensregulatespainlikebehaviourandsleep
AT husuwan acommonneuronalensembleinnucleusaccumbensregulatespainlikebehaviourandsleep
AT dinghailei acommonneuronalensembleinnucleusaccumbensregulatespainlikebehaviourandsleep
AT anshuming acommonneuronalensembleinnucleusaccumbensregulatespainlikebehaviourandsleep
AT caojunli acommonneuronalensembleinnucleusaccumbensregulatespainlikebehaviourandsleep
AT sunhaiyan commonneuronalensembleinnucleusaccumbensregulatespainlikebehaviourandsleep
AT lizhilin commonneuronalensembleinnucleusaccumbensregulatespainlikebehaviourandsleep
AT qiuzhentong commonneuronalensembleinnucleusaccumbensregulatespainlikebehaviourandsleep
AT shenyu commonneuronalensembleinnucleusaccumbensregulatespainlikebehaviourandsleep
AT guoqingchen commonneuronalensembleinnucleusaccumbensregulatespainlikebehaviourandsleep
AT husuwan commonneuronalensembleinnucleusaccumbensregulatespainlikebehaviourandsleep
AT dinghailei commonneuronalensembleinnucleusaccumbensregulatespainlikebehaviourandsleep
AT anshuming commonneuronalensembleinnucleusaccumbensregulatespainlikebehaviourandsleep
AT caojunli commonneuronalensembleinnucleusaccumbensregulatespainlikebehaviourandsleep