Cargando…

Inhibitory insula-ACC projections modulate affective but not sensory aspects of neuropathic pain

The insula and anterior cingulate cortex (ACC) are brain regions that undergo structural and functional reorganization in neuropathic pain states. Here, we aimed to study inhibitory parvalbumin positive (PV+) posterior insula (pIC) to posterior ACC (pACC) projections, and to evaluate the effects of...

Descripción completa

Detalles Bibliográficos
Autores principales: Alonso-Matielo, Heloísa, Zhang, Zizhen, Gambeta, Eder, Huang, Junting, Chen, Lina, de Melo, Gabriel Oliveira, Dale, Camila Squarzoni, Zamponi, Gerald W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10440912/
https://www.ncbi.nlm.nih.gov/pubmed/37605272
http://dx.doi.org/10.1186/s13041-023-01052-8
_version_ 1785093255542603776
author Alonso-Matielo, Heloísa
Zhang, Zizhen
Gambeta, Eder
Huang, Junting
Chen, Lina
de Melo, Gabriel Oliveira
Dale, Camila Squarzoni
Zamponi, Gerald W.
author_facet Alonso-Matielo, Heloísa
Zhang, Zizhen
Gambeta, Eder
Huang, Junting
Chen, Lina
de Melo, Gabriel Oliveira
Dale, Camila Squarzoni
Zamponi, Gerald W.
author_sort Alonso-Matielo, Heloísa
collection PubMed
description The insula and anterior cingulate cortex (ACC) are brain regions that undergo structural and functional reorganization in neuropathic pain states. Here, we aimed to study inhibitory parvalbumin positive (PV+) posterior insula (pIC) to posterior ACC (pACC) projections, and to evaluate the effects of direct optogenetic manipulation of such projections on mechanical nociception and spontaneous ongoing pain in mice with Spared Nerve Injury (SNI). CTB(488) tract-tracing in male PVCrexAi9 mice revealed a small proportion of PV+ projections from the pIC to the pACC. Electrophysiological analysis confirmed the existence of synaptic inputs into the pACC by pIC GABAergic cells. Optogenetic stimulation of these pathways did not change mechanical nociception, but induced conditioned place preference behavior responses. Our results suggest the presence of inhibitory projections between the pIC and the pACC which are able to selectively modulate affective aspects of neuropathic pain. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13041-023-01052-8.
format Online
Article
Text
id pubmed-10440912
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-104409122023-08-22 Inhibitory insula-ACC projections modulate affective but not sensory aspects of neuropathic pain Alonso-Matielo, Heloísa Zhang, Zizhen Gambeta, Eder Huang, Junting Chen, Lina de Melo, Gabriel Oliveira Dale, Camila Squarzoni Zamponi, Gerald W. Mol Brain Micro Report The insula and anterior cingulate cortex (ACC) are brain regions that undergo structural and functional reorganization in neuropathic pain states. Here, we aimed to study inhibitory parvalbumin positive (PV+) posterior insula (pIC) to posterior ACC (pACC) projections, and to evaluate the effects of direct optogenetic manipulation of such projections on mechanical nociception and spontaneous ongoing pain in mice with Spared Nerve Injury (SNI). CTB(488) tract-tracing in male PVCrexAi9 mice revealed a small proportion of PV+ projections from the pIC to the pACC. Electrophysiological analysis confirmed the existence of synaptic inputs into the pACC by pIC GABAergic cells. Optogenetic stimulation of these pathways did not change mechanical nociception, but induced conditioned place preference behavior responses. Our results suggest the presence of inhibitory projections between the pIC and the pACC which are able to selectively modulate affective aspects of neuropathic pain. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13041-023-01052-8. BioMed Central 2023-08-21 /pmc/articles/PMC10440912/ /pubmed/37605272 http://dx.doi.org/10.1186/s13041-023-01052-8 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Micro Report
Alonso-Matielo, Heloísa
Zhang, Zizhen
Gambeta, Eder
Huang, Junting
Chen, Lina
de Melo, Gabriel Oliveira
Dale, Camila Squarzoni
Zamponi, Gerald W.
Inhibitory insula-ACC projections modulate affective but not sensory aspects of neuropathic pain
title Inhibitory insula-ACC projections modulate affective but not sensory aspects of neuropathic pain
title_full Inhibitory insula-ACC projections modulate affective but not sensory aspects of neuropathic pain
title_fullStr Inhibitory insula-ACC projections modulate affective but not sensory aspects of neuropathic pain
title_full_unstemmed Inhibitory insula-ACC projections modulate affective but not sensory aspects of neuropathic pain
title_short Inhibitory insula-ACC projections modulate affective but not sensory aspects of neuropathic pain
title_sort inhibitory insula-acc projections modulate affective but not sensory aspects of neuropathic pain
topic Micro Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10440912/
https://www.ncbi.nlm.nih.gov/pubmed/37605272
http://dx.doi.org/10.1186/s13041-023-01052-8
work_keys_str_mv AT alonsomatieloheloisa inhibitoryinsulaaccprojectionsmodulateaffectivebutnotsensoryaspectsofneuropathicpain
AT zhangzizhen inhibitoryinsulaaccprojectionsmodulateaffectivebutnotsensoryaspectsofneuropathicpain
AT gambetaeder inhibitoryinsulaaccprojectionsmodulateaffectivebutnotsensoryaspectsofneuropathicpain
AT huangjunting inhibitoryinsulaaccprojectionsmodulateaffectivebutnotsensoryaspectsofneuropathicpain
AT chenlina inhibitoryinsulaaccprojectionsmodulateaffectivebutnotsensoryaspectsofneuropathicpain
AT demelogabrieloliveira inhibitoryinsulaaccprojectionsmodulateaffectivebutnotsensoryaspectsofneuropathicpain
AT dalecamilasquarzoni inhibitoryinsulaaccprojectionsmodulateaffectivebutnotsensoryaspectsofneuropathicpain
AT zamponigeraldw inhibitoryinsulaaccprojectionsmodulateaffectivebutnotsensoryaspectsofneuropathicpain