Cargando…

Projections from the Rostral Zona Incerta to the Thalamic Paraventricular Nucleus Mediate Nociceptive Neurotransmission in Mice

Zona incerta (ZI) is an integrative subthalamic region in nociceptive neurotransmission. Previous studies demonstrated that the rostral ZI (ZIR) is an important gamma–aminobutyric acid-ergic (GABAergic) source to the thalamic paraventricular nucleus (PVT), but whether the ZIR–PVT pathway participate...

Descripción completa

Detalles Bibliográficos
Autores principales: Wu, Feng-Ling, Chen, Si-Hai, Li, Jia-Ni, Zhao, Liu-Jie, Wu, Xue-Mei, Hong, Jie, Zhu, Ke-Hua, Sun, Han-Xue, Shi, Su-Juan, Mao, E, Zang, Wei-Dong, Cao, Jing, Kou, Zhen-Zhen, Li, Yun-Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9966812/
https://www.ncbi.nlm.nih.gov/pubmed/36837844
http://dx.doi.org/10.3390/metabo13020226
_version_ 1784897109724495872
author Wu, Feng-Ling
Chen, Si-Hai
Li, Jia-Ni
Zhao, Liu-Jie
Wu, Xue-Mei
Hong, Jie
Zhu, Ke-Hua
Sun, Han-Xue
Shi, Su-Juan
Mao, E
Zang, Wei-Dong
Cao, Jing
Kou, Zhen-Zhen
Li, Yun-Qing
author_facet Wu, Feng-Ling
Chen, Si-Hai
Li, Jia-Ni
Zhao, Liu-Jie
Wu, Xue-Mei
Hong, Jie
Zhu, Ke-Hua
Sun, Han-Xue
Shi, Su-Juan
Mao, E
Zang, Wei-Dong
Cao, Jing
Kou, Zhen-Zhen
Li, Yun-Qing
author_sort Wu, Feng-Ling
collection PubMed
description Zona incerta (ZI) is an integrative subthalamic region in nociceptive neurotransmission. Previous studies demonstrated that the rostral ZI (ZIR) is an important gamma–aminobutyric acid-ergic (GABAergic) source to the thalamic paraventricular nucleus (PVT), but whether the ZIR–PVT pathway participates in nociceptive modulation is still unclear. Therefore, our investigation utilized anatomical tracing, fiber photometry, chemogenetic, optogenetic and local pharmacological approaches to investigate the roles of the ZIR(GABA+)–PVT pathway in nociceptive neurotransmission in mice. We found that projections from the GABAergic neurons in ZIR to PVT were involved in nociceptive neurotransmission. Furthermore, chemogenetic and optogenetic activation of the ZIR(GABA+)–PVT pathway alleviates pain, whereas inhibiting the activities of the ZIR(GABA+)-PVT circuit induces mechanical hypersensitivity and partial heat hyperalgesia. Importantly, in vivo pharmacology combined with optogenetics revealed that the GABA-A receptor (GABA(A)R) is crucial for GABAergic inhibition from ZIR to PVT. Our data suggest that the ZIR(GABA+)–PVT pathway acts through GABA(A)R-expressing glutamatergic neurons in PVT mediates nociceptive neurotransmission.
format Online
Article
Text
id pubmed-9966812
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-99668122023-02-26 Projections from the Rostral Zona Incerta to the Thalamic Paraventricular Nucleus Mediate Nociceptive Neurotransmission in Mice Wu, Feng-Ling Chen, Si-Hai Li, Jia-Ni Zhao, Liu-Jie Wu, Xue-Mei Hong, Jie Zhu, Ke-Hua Sun, Han-Xue Shi, Su-Juan Mao, E Zang, Wei-Dong Cao, Jing Kou, Zhen-Zhen Li, Yun-Qing Metabolites Article Zona incerta (ZI) is an integrative subthalamic region in nociceptive neurotransmission. Previous studies demonstrated that the rostral ZI (ZIR) is an important gamma–aminobutyric acid-ergic (GABAergic) source to the thalamic paraventricular nucleus (PVT), but whether the ZIR–PVT pathway participates in nociceptive modulation is still unclear. Therefore, our investigation utilized anatomical tracing, fiber photometry, chemogenetic, optogenetic and local pharmacological approaches to investigate the roles of the ZIR(GABA+)–PVT pathway in nociceptive neurotransmission in mice. We found that projections from the GABAergic neurons in ZIR to PVT were involved in nociceptive neurotransmission. Furthermore, chemogenetic and optogenetic activation of the ZIR(GABA+)–PVT pathway alleviates pain, whereas inhibiting the activities of the ZIR(GABA+)-PVT circuit induces mechanical hypersensitivity and partial heat hyperalgesia. Importantly, in vivo pharmacology combined with optogenetics revealed that the GABA-A receptor (GABA(A)R) is crucial for GABAergic inhibition from ZIR to PVT. Our data suggest that the ZIR(GABA+)–PVT pathway acts through GABA(A)R-expressing glutamatergic neurons in PVT mediates nociceptive neurotransmission. MDPI 2023-02-03 /pmc/articles/PMC9966812/ /pubmed/36837844 http://dx.doi.org/10.3390/metabo13020226 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Wu, Feng-Ling
Chen, Si-Hai
Li, Jia-Ni
Zhao, Liu-Jie
Wu, Xue-Mei
Hong, Jie
Zhu, Ke-Hua
Sun, Han-Xue
Shi, Su-Juan
Mao, E
Zang, Wei-Dong
Cao, Jing
Kou, Zhen-Zhen
Li, Yun-Qing
Projections from the Rostral Zona Incerta to the Thalamic Paraventricular Nucleus Mediate Nociceptive Neurotransmission in Mice
title Projections from the Rostral Zona Incerta to the Thalamic Paraventricular Nucleus Mediate Nociceptive Neurotransmission in Mice
title_full Projections from the Rostral Zona Incerta to the Thalamic Paraventricular Nucleus Mediate Nociceptive Neurotransmission in Mice
title_fullStr Projections from the Rostral Zona Incerta to the Thalamic Paraventricular Nucleus Mediate Nociceptive Neurotransmission in Mice
title_full_unstemmed Projections from the Rostral Zona Incerta to the Thalamic Paraventricular Nucleus Mediate Nociceptive Neurotransmission in Mice
title_short Projections from the Rostral Zona Incerta to the Thalamic Paraventricular Nucleus Mediate Nociceptive Neurotransmission in Mice
title_sort projections from the rostral zona incerta to the thalamic paraventricular nucleus mediate nociceptive neurotransmission in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9966812/
https://www.ncbi.nlm.nih.gov/pubmed/36837844
http://dx.doi.org/10.3390/metabo13020226
work_keys_str_mv AT wufengling projectionsfromtherostralzonaincertatothethalamicparaventricularnucleusmediatenociceptiveneurotransmissioninmice
AT chensihai projectionsfromtherostralzonaincertatothethalamicparaventricularnucleusmediatenociceptiveneurotransmissioninmice
AT lijiani projectionsfromtherostralzonaincertatothethalamicparaventricularnucleusmediatenociceptiveneurotransmissioninmice
AT zhaoliujie projectionsfromtherostralzonaincertatothethalamicparaventricularnucleusmediatenociceptiveneurotransmissioninmice
AT wuxuemei projectionsfromtherostralzonaincertatothethalamicparaventricularnucleusmediatenociceptiveneurotransmissioninmice
AT hongjie projectionsfromtherostralzonaincertatothethalamicparaventricularnucleusmediatenociceptiveneurotransmissioninmice
AT zhukehua projectionsfromtherostralzonaincertatothethalamicparaventricularnucleusmediatenociceptiveneurotransmissioninmice
AT sunhanxue projectionsfromtherostralzonaincertatothethalamicparaventricularnucleusmediatenociceptiveneurotransmissioninmice
AT shisujuan projectionsfromtherostralzonaincertatothethalamicparaventricularnucleusmediatenociceptiveneurotransmissioninmice
AT maoe projectionsfromtherostralzonaincertatothethalamicparaventricularnucleusmediatenociceptiveneurotransmissioninmice
AT zangweidong projectionsfromtherostralzonaincertatothethalamicparaventricularnucleusmediatenociceptiveneurotransmissioninmice
AT caojing projectionsfromtherostralzonaincertatothethalamicparaventricularnucleusmediatenociceptiveneurotransmissioninmice
AT kouzhenzhen projectionsfromtherostralzonaincertatothethalamicparaventricularnucleusmediatenociceptiveneurotransmissioninmice
AT liyunqing projectionsfromtherostralzonaincertatothethalamicparaventricularnucleusmediatenociceptiveneurotransmissioninmice