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Decreased Resting Functional Connectivity after Traumatic Brain Injury in the Rat
Traumatic brain injury (TBI) contributes to about 10% of acquired epilepsy. Even though the mechanisms of post-traumatic epileptogenesis are poorly known, a disruption of neuronal networks predisposing to altered neuronal synchrony remains a viable candidate mechanism. We tested a hypothesis that re...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3991600/ https://www.ncbi.nlm.nih.gov/pubmed/24748279 http://dx.doi.org/10.1371/journal.pone.0095280 |
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author | Mishra, Asht Mangal Bai, Xiaoxiao Sanganahalli, Basavaraju G. Waxman, Stephen G. Shatillo, Olena Grohn, Olli Hyder, Fahmeed Pitkänen, Asla Blumenfeld, Hal |
author_facet | Mishra, Asht Mangal Bai, Xiaoxiao Sanganahalli, Basavaraju G. Waxman, Stephen G. Shatillo, Olena Grohn, Olli Hyder, Fahmeed Pitkänen, Asla Blumenfeld, Hal |
author_sort | Mishra, Asht Mangal |
collection | PubMed |
description | Traumatic brain injury (TBI) contributes to about 10% of acquired epilepsy. Even though the mechanisms of post-traumatic epileptogenesis are poorly known, a disruption of neuronal networks predisposing to altered neuronal synchrony remains a viable candidate mechanism. We tested a hypothesis that resting state BOLD-fMRI functional connectivity can reveal network abnormalities in brain regions that are connected to the lesioned cortex, and that these changes associate with functional impairment, particularly epileptogenesis. TBI was induced using lateral fluid-percussion injury in seven adult male Sprague-Dawley rats followed by functional imaging at 9.4T 4 months later. As controls we used six sham-operated animals that underwent all surgical operations but were not injured. Electroencephalogram (EEG)-functional magnetic resonance imaging (fMRI) was performed to measure resting functional connectivity. A week after functional imaging, rats were implanted with bipolar skull electrodes. After recovery, rats underwent pentyleneterazol (PTZ) seizure-susceptibility test under EEG. For image analysis, four pairs of regions of interests were analyzed in each hemisphere: ipsilateral and contralateral frontal and parietal cortex, hippocampus, and thalamus. High-pass and low-pass filters were applied to functional imaging data. Group statistics comparing injured and sham-operated rats and correlations over time between each region were calculated. In the end, rats were perfused for histology. None of the rats had epileptiform discharges during functional imaging. PTZ-test, however revealed increased seizure susceptibility in injured rats as compared to controls. Group statistics revealed decreased connectivity between the ipsilateral and contralateral parietal cortex and between the parietal cortex and hippocampus on the side of injury as compared to sham-operated animals. Injured animals also had abnormal negative connectivity between the ipsilateral and contralateral parietal cortex and other regions. Our data provide the first evidence on abnormal functional connectivity after experimental TBI assessed with resting state BOLD-fMRI. |
format | Online Article Text |
id | pubmed-3991600 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-39916002014-04-21 Decreased Resting Functional Connectivity after Traumatic Brain Injury in the Rat Mishra, Asht Mangal Bai, Xiaoxiao Sanganahalli, Basavaraju G. Waxman, Stephen G. Shatillo, Olena Grohn, Olli Hyder, Fahmeed Pitkänen, Asla Blumenfeld, Hal PLoS One Research Article Traumatic brain injury (TBI) contributes to about 10% of acquired epilepsy. Even though the mechanisms of post-traumatic epileptogenesis are poorly known, a disruption of neuronal networks predisposing to altered neuronal synchrony remains a viable candidate mechanism. We tested a hypothesis that resting state BOLD-fMRI functional connectivity can reveal network abnormalities in brain regions that are connected to the lesioned cortex, and that these changes associate with functional impairment, particularly epileptogenesis. TBI was induced using lateral fluid-percussion injury in seven adult male Sprague-Dawley rats followed by functional imaging at 9.4T 4 months later. As controls we used six sham-operated animals that underwent all surgical operations but were not injured. Electroencephalogram (EEG)-functional magnetic resonance imaging (fMRI) was performed to measure resting functional connectivity. A week after functional imaging, rats were implanted with bipolar skull electrodes. After recovery, rats underwent pentyleneterazol (PTZ) seizure-susceptibility test under EEG. For image analysis, four pairs of regions of interests were analyzed in each hemisphere: ipsilateral and contralateral frontal and parietal cortex, hippocampus, and thalamus. High-pass and low-pass filters were applied to functional imaging data. Group statistics comparing injured and sham-operated rats and correlations over time between each region were calculated. In the end, rats were perfused for histology. None of the rats had epileptiform discharges during functional imaging. PTZ-test, however revealed increased seizure susceptibility in injured rats as compared to controls. Group statistics revealed decreased connectivity between the ipsilateral and contralateral parietal cortex and between the parietal cortex and hippocampus on the side of injury as compared to sham-operated animals. Injured animals also had abnormal negative connectivity between the ipsilateral and contralateral parietal cortex and other regions. Our data provide the first evidence on abnormal functional connectivity after experimental TBI assessed with resting state BOLD-fMRI. Public Library of Science 2014-04-18 /pmc/articles/PMC3991600/ /pubmed/24748279 http://dx.doi.org/10.1371/journal.pone.0095280 Text en © 2014 Mishra et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Mishra, Asht Mangal Bai, Xiaoxiao Sanganahalli, Basavaraju G. Waxman, Stephen G. Shatillo, Olena Grohn, Olli Hyder, Fahmeed Pitkänen, Asla Blumenfeld, Hal Decreased Resting Functional Connectivity after Traumatic Brain Injury in the Rat |
title | Decreased Resting Functional Connectivity after Traumatic Brain Injury in the Rat |
title_full | Decreased Resting Functional Connectivity after Traumatic Brain Injury in the Rat |
title_fullStr | Decreased Resting Functional Connectivity after Traumatic Brain Injury in the Rat |
title_full_unstemmed | Decreased Resting Functional Connectivity after Traumatic Brain Injury in the Rat |
title_short | Decreased Resting Functional Connectivity after Traumatic Brain Injury in the Rat |
title_sort | decreased resting functional connectivity after traumatic brain injury in the rat |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3991600/ https://www.ncbi.nlm.nih.gov/pubmed/24748279 http://dx.doi.org/10.1371/journal.pone.0095280 |
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