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Resting-sate functional reorganization of the rat limbic system following neuropathic injury
Human brain imaging studies from various clinical cohorts show that chronic pain is associated with large-scale brain functional and morphological reorganization. However, how the rat whole-brain network is topologically reorganized to support persistent pain-like behavior following neuropathic inju...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4151103/ https://www.ncbi.nlm.nih.gov/pubmed/25178478 http://dx.doi.org/10.1038/srep06186 |
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author | Baliki, M. N. Chang, P. C. Baria, A. T. Centeno, M. V. Apkarian, A. V. |
author_facet | Baliki, M. N. Chang, P. C. Baria, A. T. Centeno, M. V. Apkarian, A. V. |
author_sort | Baliki, M. N. |
collection | PubMed |
description | Human brain imaging studies from various clinical cohorts show that chronic pain is associated with large-scale brain functional and morphological reorganization. However, how the rat whole-brain network is topologically reorganized to support persistent pain-like behavior following neuropathic injury remains unknown. Here we compare resting state fMRI functional connectivity-based whole-brain network properties between rats receiving spared nerve injury (SNI) vs. sham injury, at 5 days (n = 11 SNI; n = 12 sham) and 28 days (n = 11 SNI; n = 12 sham) post-injury. Similar to the human, the rat brain topological properties exhibited small world features and did not differ between SNI and sham. Local neural networks in SNI animals showed minimal disruption at day 5, and more extensive reorganization at day 28 post-injury. Twenty-eight days after SNI, functional connection changes were localized mainly to within the limbic system, as well as between the limbic and nociceptive systems. No connectivity changes were observed within the nociceptive network. Furthermore, these changes were lateralized and in proportion to the tactile allodynia exhibited by SNI animals. The findings establish that SNI is primarily associated with altered information transfer of limbic regions and provides a novel translational framework for understanding brain functional reorganization in response to a persistent neuropathic injury. |
format | Online Article Text |
id | pubmed-4151103 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-41511032014-09-08 Resting-sate functional reorganization of the rat limbic system following neuropathic injury Baliki, M. N. Chang, P. C. Baria, A. T. Centeno, M. V. Apkarian, A. V. Sci Rep Article Human brain imaging studies from various clinical cohorts show that chronic pain is associated with large-scale brain functional and morphological reorganization. However, how the rat whole-brain network is topologically reorganized to support persistent pain-like behavior following neuropathic injury remains unknown. Here we compare resting state fMRI functional connectivity-based whole-brain network properties between rats receiving spared nerve injury (SNI) vs. sham injury, at 5 days (n = 11 SNI; n = 12 sham) and 28 days (n = 11 SNI; n = 12 sham) post-injury. Similar to the human, the rat brain topological properties exhibited small world features and did not differ between SNI and sham. Local neural networks in SNI animals showed minimal disruption at day 5, and more extensive reorganization at day 28 post-injury. Twenty-eight days after SNI, functional connection changes were localized mainly to within the limbic system, as well as between the limbic and nociceptive systems. No connectivity changes were observed within the nociceptive network. Furthermore, these changes were lateralized and in proportion to the tactile allodynia exhibited by SNI animals. The findings establish that SNI is primarily associated with altered information transfer of limbic regions and provides a novel translational framework for understanding brain functional reorganization in response to a persistent neuropathic injury. Nature Publishing Group 2014-09-02 /pmc/articles/PMC4151103/ /pubmed/25178478 http://dx.doi.org/10.1038/srep06186 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Article Baliki, M. N. Chang, P. C. Baria, A. T. Centeno, M. V. Apkarian, A. V. Resting-sate functional reorganization of the rat limbic system following neuropathic injury |
title | Resting-sate functional reorganization of the rat limbic system following neuropathic injury |
title_full | Resting-sate functional reorganization of the rat limbic system following neuropathic injury |
title_fullStr | Resting-sate functional reorganization of the rat limbic system following neuropathic injury |
title_full_unstemmed | Resting-sate functional reorganization of the rat limbic system following neuropathic injury |
title_short | Resting-sate functional reorganization of the rat limbic system following neuropathic injury |
title_sort | resting-sate functional reorganization of the rat limbic system following neuropathic injury |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4151103/ https://www.ncbi.nlm.nih.gov/pubmed/25178478 http://dx.doi.org/10.1038/srep06186 |
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