Cargando…
Retrosplenial Cortex Contributes to Network Changes during Seizures in the GAERS Absence Epilepsy Rat Model
Resting state-fMRI was performed to explore brain networks in Genetic Absence Epilepsy Rats from Strasbourg and in nonepileptic controls (NEC) during monitoring of the brain state by simultaneous optical Ca(2+)-recordings. Graph theoretical analysis allowed for the identification of acute and chroni...
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/PMC8263073/ https://www.ncbi.nlm.nih.gov/pubmed/34296168 http://dx.doi.org/10.1093/texcom/tgab023 |
_version_ | 1783719310524416000 |
---|---|
author | Wachsmuth, Lydia Datunashvili, Maia Kemper, Katharina Albers, Franziska Lambers, Henriette Lüttjohann, Annika Kreitz, Silke Budde, Thomas Faber, Cornelius |
author_facet | Wachsmuth, Lydia Datunashvili, Maia Kemper, Katharina Albers, Franziska Lambers, Henriette Lüttjohann, Annika Kreitz, Silke Budde, Thomas Faber, Cornelius |
author_sort | Wachsmuth, Lydia |
collection | PubMed |
description | Resting state-fMRI was performed to explore brain networks in Genetic Absence Epilepsy Rats from Strasbourg and in nonepileptic controls (NEC) during monitoring of the brain state by simultaneous optical Ca(2+)-recordings. Graph theoretical analysis allowed for the identification of acute and chronic network changes and revealed preserved small world topology before and after seizure onset. The most prominent acute change in network organization during seizures was the segregation of cortical regions from the remaining brain. Stronger connections between thalamic with limbic regions compared with preseizure state indicated network regularization during seizures. When comparing between strains, intrathalamic connections were prominent in NEC, on local level represented by higher thalamic strengths and hub scores. Subtle differences were observed for retrosplenial cortex (RS), forming more connections beyond cortex in epileptic rats, and showing a tendency to lateralization during seizures. A potential role of RS as hub between subcortical and cortical regions in epilepsy was supported by increased numbers of parvalbumin-positive (PV+) interneurons together with enhanced inhibitory synaptic activity and neuronal excitability in pyramidal neurons. By combining multimodal fMRI data, graph theoretical methods, and electrophysiological recordings, we identified the RS as promising target for modulation of seizure activity and/or comorbidities. |
format | Online Article Text |
id | pubmed-8263073 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-82630732021-07-21 Retrosplenial Cortex Contributes to Network Changes during Seizures in the GAERS Absence Epilepsy Rat Model Wachsmuth, Lydia Datunashvili, Maia Kemper, Katharina Albers, Franziska Lambers, Henriette Lüttjohann, Annika Kreitz, Silke Budde, Thomas Faber, Cornelius Cereb Cortex Commun Original Article Resting state-fMRI was performed to explore brain networks in Genetic Absence Epilepsy Rats from Strasbourg and in nonepileptic controls (NEC) during monitoring of the brain state by simultaneous optical Ca(2+)-recordings. Graph theoretical analysis allowed for the identification of acute and chronic network changes and revealed preserved small world topology before and after seizure onset. The most prominent acute change in network organization during seizures was the segregation of cortical regions from the remaining brain. Stronger connections between thalamic with limbic regions compared with preseizure state indicated network regularization during seizures. When comparing between strains, intrathalamic connections were prominent in NEC, on local level represented by higher thalamic strengths and hub scores. Subtle differences were observed for retrosplenial cortex (RS), forming more connections beyond cortex in epileptic rats, and showing a tendency to lateralization during seizures. A potential role of RS as hub between subcortical and cortical regions in epilepsy was supported by increased numbers of parvalbumin-positive (PV+) interneurons together with enhanced inhibitory synaptic activity and neuronal excitability in pyramidal neurons. By combining multimodal fMRI data, graph theoretical methods, and electrophysiological recordings, we identified the RS as promising target for modulation of seizure activity and/or comorbidities. Oxford University Press 2021-03-23 /pmc/articles/PMC8263073/ /pubmed/34296168 http://dx.doi.org/10.1093/texcom/tgab023 Text en © The Author(s) 2021. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Wachsmuth, Lydia Datunashvili, Maia Kemper, Katharina Albers, Franziska Lambers, Henriette Lüttjohann, Annika Kreitz, Silke Budde, Thomas Faber, Cornelius Retrosplenial Cortex Contributes to Network Changes during Seizures in the GAERS Absence Epilepsy Rat Model |
title | Retrosplenial Cortex Contributes to Network Changes during Seizures in the GAERS Absence Epilepsy Rat Model |
title_full | Retrosplenial Cortex Contributes to Network Changes during Seizures in the GAERS Absence Epilepsy Rat Model |
title_fullStr | Retrosplenial Cortex Contributes to Network Changes during Seizures in the GAERS Absence Epilepsy Rat Model |
title_full_unstemmed | Retrosplenial Cortex Contributes to Network Changes during Seizures in the GAERS Absence Epilepsy Rat Model |
title_short | Retrosplenial Cortex Contributes to Network Changes during Seizures in the GAERS Absence Epilepsy Rat Model |
title_sort | retrosplenial cortex contributes to network changes during seizures in the gaers absence epilepsy rat model |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8263073/ https://www.ncbi.nlm.nih.gov/pubmed/34296168 http://dx.doi.org/10.1093/texcom/tgab023 |
work_keys_str_mv | AT wachsmuthlydia retrosplenialcortexcontributestonetworkchangesduringseizuresinthegaersabsenceepilepsyratmodel AT datunashvilimaia retrosplenialcortexcontributestonetworkchangesduringseizuresinthegaersabsenceepilepsyratmodel AT kemperkatharina retrosplenialcortexcontributestonetworkchangesduringseizuresinthegaersabsenceepilepsyratmodel AT albersfranziska retrosplenialcortexcontributestonetworkchangesduringseizuresinthegaersabsenceepilepsyratmodel AT lambershenriette retrosplenialcortexcontributestonetworkchangesduringseizuresinthegaersabsenceepilepsyratmodel AT luttjohannannika retrosplenialcortexcontributestonetworkchangesduringseizuresinthegaersabsenceepilepsyratmodel AT kreitzsilke retrosplenialcortexcontributestonetworkchangesduringseizuresinthegaersabsenceepilepsyratmodel AT buddethomas retrosplenialcortexcontributestonetworkchangesduringseizuresinthegaersabsenceepilepsyratmodel AT fabercornelius retrosplenialcortexcontributestonetworkchangesduringseizuresinthegaersabsenceepilepsyratmodel |