Cargando…
Compensatory functional connectome changes in a rat model of traumatic brain injury
Penetrating cortical impact injuries alter neuronal communication beyond the injury epicentre, across regions involved in affective, sensorimotor and cognitive processing. Understanding how traumatic brain injury reorganizes local and brain wide nodal interactions may provide valuable quantitative p...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8557657/ https://www.ncbi.nlm.nih.gov/pubmed/34729482 http://dx.doi.org/10.1093/braincomms/fcab244 |
_version_ | 1784592414279729152 |
---|---|
author | Yang, Zhihui Zhu, Tian Pompilus, Marjory Fu, Yueqiang Zhu, Jiepei Arjona, Kefren Arja, Rawad Daniel Grudny, Matteo M Plant, H Daniel Bose, Prodip Wang, Kevin K Febo, Marcelo |
author_facet | Yang, Zhihui Zhu, Tian Pompilus, Marjory Fu, Yueqiang Zhu, Jiepei Arjona, Kefren Arja, Rawad Daniel Grudny, Matteo M Plant, H Daniel Bose, Prodip Wang, Kevin K Febo, Marcelo |
author_sort | Yang, Zhihui |
collection | PubMed |
description | Penetrating cortical impact injuries alter neuronal communication beyond the injury epicentre, across regions involved in affective, sensorimotor and cognitive processing. Understanding how traumatic brain injury reorganizes local and brain wide nodal interactions may provide valuable quantitative parameters for monitoring pathological progression and recovery. To this end, we investigated spontaneous fluctuations in the functional MRI signal obtained at 11.1 T in rats sustaining controlled cortical impact and imaged at 2- and 30-days post-injury. Graph theory-based calculations were applied to weighted undirected matrices constructed from 12 879 pairwise correlations between functional MRI signals from 162 regions. Our data indicate that on Days 2 and 30 post-controlled cortical impact there is a significant increase in connectivity strength in nodes located in contralesional cortical, thalamic and basal forebrain areas. Rats imaged on Day 2 post-injury had significantly greater network modularity than controls, with influential nodes (with high eigenvector centrality) contained within the contralesional module and participating less in cross-modular interactions. By Day 30, modularity and cross-modular interactions recover, although a cluster of nodes with low strength and low eigenvector centrality remain in the ipsilateral cortex. Our results suggest that changes in node strength, modularity, eigenvector centrality and participation coefficient track early and late traumatic brain injury effects on brain functional connectivity. We propose that the observed compensatory functional connectivity reorganization in response to controlled cortical impact may be unfavourable to brain wide communication in the early post-injury period. |
format | Online Article Text |
id | pubmed-8557657 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-85576572021-11-01 Compensatory functional connectome changes in a rat model of traumatic brain injury Yang, Zhihui Zhu, Tian Pompilus, Marjory Fu, Yueqiang Zhu, Jiepei Arjona, Kefren Arja, Rawad Daniel Grudny, Matteo M Plant, H Daniel Bose, Prodip Wang, Kevin K Febo, Marcelo Brain Commun Original Article Penetrating cortical impact injuries alter neuronal communication beyond the injury epicentre, across regions involved in affective, sensorimotor and cognitive processing. Understanding how traumatic brain injury reorganizes local and brain wide nodal interactions may provide valuable quantitative parameters for monitoring pathological progression and recovery. To this end, we investigated spontaneous fluctuations in the functional MRI signal obtained at 11.1 T in rats sustaining controlled cortical impact and imaged at 2- and 30-days post-injury. Graph theory-based calculations were applied to weighted undirected matrices constructed from 12 879 pairwise correlations between functional MRI signals from 162 regions. Our data indicate that on Days 2 and 30 post-controlled cortical impact there is a significant increase in connectivity strength in nodes located in contralesional cortical, thalamic and basal forebrain areas. Rats imaged on Day 2 post-injury had significantly greater network modularity than controls, with influential nodes (with high eigenvector centrality) contained within the contralesional module and participating less in cross-modular interactions. By Day 30, modularity and cross-modular interactions recover, although a cluster of nodes with low strength and low eigenvector centrality remain in the ipsilateral cortex. Our results suggest that changes in node strength, modularity, eigenvector centrality and participation coefficient track early and late traumatic brain injury effects on brain functional connectivity. We propose that the observed compensatory functional connectivity reorganization in response to controlled cortical impact may be unfavourable to brain wide communication in the early post-injury period. Oxford University Press 2021-10-23 /pmc/articles/PMC8557657/ /pubmed/34729482 http://dx.doi.org/10.1093/braincomms/fcab244 Text en © The Author(s) (2021). Published by Oxford University Press on behalf of the Guarantors of Brain. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Original Article Yang, Zhihui Zhu, Tian Pompilus, Marjory Fu, Yueqiang Zhu, Jiepei Arjona, Kefren Arja, Rawad Daniel Grudny, Matteo M Plant, H Daniel Bose, Prodip Wang, Kevin K Febo, Marcelo Compensatory functional connectome changes in a rat model of traumatic brain injury |
title | Compensatory functional connectome changes in a rat model of traumatic brain injury |
title_full | Compensatory functional connectome changes in a rat model of traumatic brain injury |
title_fullStr | Compensatory functional connectome changes in a rat model of traumatic brain injury |
title_full_unstemmed | Compensatory functional connectome changes in a rat model of traumatic brain injury |
title_short | Compensatory functional connectome changes in a rat model of traumatic brain injury |
title_sort | compensatory functional connectome changes in a rat model of traumatic brain injury |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8557657/ https://www.ncbi.nlm.nih.gov/pubmed/34729482 http://dx.doi.org/10.1093/braincomms/fcab244 |
work_keys_str_mv | AT yangzhihui compensatoryfunctionalconnectomechangesinaratmodeloftraumaticbraininjury AT zhutian compensatoryfunctionalconnectomechangesinaratmodeloftraumaticbraininjury AT pompilusmarjory compensatoryfunctionalconnectomechangesinaratmodeloftraumaticbraininjury AT fuyueqiang compensatoryfunctionalconnectomechangesinaratmodeloftraumaticbraininjury AT zhujiepei compensatoryfunctionalconnectomechangesinaratmodeloftraumaticbraininjury AT arjonakefren compensatoryfunctionalconnectomechangesinaratmodeloftraumaticbraininjury AT arjarawaddaniel compensatoryfunctionalconnectomechangesinaratmodeloftraumaticbraininjury AT grudnymatteom compensatoryfunctionalconnectomechangesinaratmodeloftraumaticbraininjury AT planthdaniel compensatoryfunctionalconnectomechangesinaratmodeloftraumaticbraininjury AT boseprodip compensatoryfunctionalconnectomechangesinaratmodeloftraumaticbraininjury AT wangkevink compensatoryfunctionalconnectomechangesinaratmodeloftraumaticbraininjury AT febomarcelo compensatoryfunctionalconnectomechangesinaratmodeloftraumaticbraininjury |