Cargando…

Prolonged Suppression of Neuropathic Hypersensitivity upon Neurostimulation of the Posterior Insula in Mice

Neurostimulation-based therapeutic approaches are emerging as alternatives to pharmacological drugs, but need further development to optimize efficacy and reduce variability. Despite its key relevance to pain, the insular cortex has not been explored in cortical neurostimulation approaches. Here, we...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Han, Gan, Zheng, Wang, Lirong, Oswald, Manfred Josef, Kuner, Rohini
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9600702/
https://www.ncbi.nlm.nih.gov/pubmed/36291169
http://dx.doi.org/10.3390/cells11203303
_version_ 1784816908758941696
author Li, Han
Gan, Zheng
Wang, Lirong
Oswald, Manfred Josef
Kuner, Rohini
author_facet Li, Han
Gan, Zheng
Wang, Lirong
Oswald, Manfred Josef
Kuner, Rohini
author_sort Li, Han
collection PubMed
description Neurostimulation-based therapeutic approaches are emerging as alternatives to pharmacological drugs, but need further development to optimize efficacy and reduce variability. Despite its key relevance to pain, the insular cortex has not been explored in cortical neurostimulation approaches. Here, we developed an approach to perform repetitive transcranial direct current stimulation of the posterior insula (PI tDCS) and studied its impact on sensory and aversive components of neuropathic pain and pain-related anxiety and the underlying neural circuitry in mice using behavioral methods, pharmacological interventions and the expression of the activity-induced gene product, Fos. We observed that repetitive PI tDCS strongly attenuates the development of neuropathic mechanical allodynia and also reverses chronically established mechanical and cold allodynia for several weeks post-treatment by employing descending opioidergic antinociceptive pathways. Pain-related anxiety, but not pain-related aversion, were inhibited by PI tDCS. These effects were associated with a long-term suppression in the activity of key areas involved in pain modulation, such as the cingulate, prefrontal and motor cortices. These data uncover the significant potential of targeting the insular cortex with the objective of pain relief and open the way for more detailed mechanistic analyses that will contribute to improving cortical neurostimulation therapies for use in the clinical management of pain.
format Online
Article
Text
id pubmed-9600702
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-96007022022-10-27 Prolonged Suppression of Neuropathic Hypersensitivity upon Neurostimulation of the Posterior Insula in Mice Li, Han Gan, Zheng Wang, Lirong Oswald, Manfred Josef Kuner, Rohini Cells Article Neurostimulation-based therapeutic approaches are emerging as alternatives to pharmacological drugs, but need further development to optimize efficacy and reduce variability. Despite its key relevance to pain, the insular cortex has not been explored in cortical neurostimulation approaches. Here, we developed an approach to perform repetitive transcranial direct current stimulation of the posterior insula (PI tDCS) and studied its impact on sensory and aversive components of neuropathic pain and pain-related anxiety and the underlying neural circuitry in mice using behavioral methods, pharmacological interventions and the expression of the activity-induced gene product, Fos. We observed that repetitive PI tDCS strongly attenuates the development of neuropathic mechanical allodynia and also reverses chronically established mechanical and cold allodynia for several weeks post-treatment by employing descending opioidergic antinociceptive pathways. Pain-related anxiety, but not pain-related aversion, were inhibited by PI tDCS. These effects were associated with a long-term suppression in the activity of key areas involved in pain modulation, such as the cingulate, prefrontal and motor cortices. These data uncover the significant potential of targeting the insular cortex with the objective of pain relief and open the way for more detailed mechanistic analyses that will contribute to improving cortical neurostimulation therapies for use in the clinical management of pain. MDPI 2022-10-20 /pmc/articles/PMC9600702/ /pubmed/36291169 http://dx.doi.org/10.3390/cells11203303 Text en © 2022 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
Li, Han
Gan, Zheng
Wang, Lirong
Oswald, Manfred Josef
Kuner, Rohini
Prolonged Suppression of Neuropathic Hypersensitivity upon Neurostimulation of the Posterior Insula in Mice
title Prolonged Suppression of Neuropathic Hypersensitivity upon Neurostimulation of the Posterior Insula in Mice
title_full Prolonged Suppression of Neuropathic Hypersensitivity upon Neurostimulation of the Posterior Insula in Mice
title_fullStr Prolonged Suppression of Neuropathic Hypersensitivity upon Neurostimulation of the Posterior Insula in Mice
title_full_unstemmed Prolonged Suppression of Neuropathic Hypersensitivity upon Neurostimulation of the Posterior Insula in Mice
title_short Prolonged Suppression of Neuropathic Hypersensitivity upon Neurostimulation of the Posterior Insula in Mice
title_sort prolonged suppression of neuropathic hypersensitivity upon neurostimulation of the posterior insula in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9600702/
https://www.ncbi.nlm.nih.gov/pubmed/36291169
http://dx.doi.org/10.3390/cells11203303
work_keys_str_mv AT lihan prolongedsuppressionofneuropathichypersensitivityuponneurostimulationoftheposteriorinsulainmice
AT ganzheng prolongedsuppressionofneuropathichypersensitivityuponneurostimulationoftheposteriorinsulainmice
AT wanglirong prolongedsuppressionofneuropathichypersensitivityuponneurostimulationoftheposteriorinsulainmice
AT oswaldmanfredjosef prolongedsuppressionofneuropathichypersensitivityuponneurostimulationoftheposteriorinsulainmice
AT kunerrohini prolongedsuppressionofneuropathichypersensitivityuponneurostimulationoftheposteriorinsulainmice