Cargando…
The effective connectivity of the seizure onset zone and ictal perfusion changes in amygdala kindled rhesus monkeys
Epileptic seizures are network-level phenomena. Hence, epilepsy may be regarded as a circuit-level disorder that cannot be understood outside this context. Better insight into the effective connectivity of the seizure onset zone and the manner in which seizure activity spreads could lead to specific...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4959940/ https://www.ncbi.nlm.nih.gov/pubmed/27489773 http://dx.doi.org/10.1016/j.nicl.2016.05.020 |
_version_ | 1782444462564179968 |
---|---|
author | Cleeren, Evy Premereur, Elsie Casteels, Cindy Goffin, Karolien Janssen, Peter Van Paesschen, Wim |
author_facet | Cleeren, Evy Premereur, Elsie Casteels, Cindy Goffin, Karolien Janssen, Peter Van Paesschen, Wim |
author_sort | Cleeren, Evy |
collection | PubMed |
description | Epileptic seizures are network-level phenomena. Hence, epilepsy may be regarded as a circuit-level disorder that cannot be understood outside this context. Better insight into the effective connectivity of the seizure onset zone and the manner in which seizure activity spreads could lead to specifically-tailored therapies for epilepsy. We applied the electrical amygdala kindling model in two rhesus monkeys until these animals displayed consistent stage IV seizures. At this stage, we investigated the effective connectivity of the amygdala by means of electrical microstimulation during fMRI (EM-fMRI). In addition, we imaged changes in perfusion during a seizure using ictal SPECT perfusion imaging. The spatial overlap between the connectivity network and the ictal perfusion network was assessed both at the regional level, by calculating Dice coefficients using anatomically defined regions of interest, and at the voxel level. The kindled amygdala was extensively connected to bilateral cortical and subcortical structures, which in many cases were connected multisynaptically to the amygdala. At the regional level, the spatial extents of many of these fMRI activations and deactivations corresponded to the respective increases and decreases in perfusion imaged during a stage IV seizure. At the voxel level, however, some regions showed residual seizure-specific activity (not overlapping with the EM-fMRI activations) or fMRI-specific activation (not overlapping with the ictal SPECT activations), indicating that frequently, only a part of a region anatomically connected to the seizure onset zone participated in seizure propagation. Thus, EM-fMRI in the amygdala of electrically-kindled monkeys reveals widespread areas that are often connected multisynaptically to the seizure focus. Seizure activity appears to spread, to a large extent, via these connected areas. |
format | Online Article Text |
id | pubmed-4959940 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-49599402016-08-03 The effective connectivity of the seizure onset zone and ictal perfusion changes in amygdala kindled rhesus monkeys Cleeren, Evy Premereur, Elsie Casteels, Cindy Goffin, Karolien Janssen, Peter Van Paesschen, Wim Neuroimage Clin Regular Article Epileptic seizures are network-level phenomena. Hence, epilepsy may be regarded as a circuit-level disorder that cannot be understood outside this context. Better insight into the effective connectivity of the seizure onset zone and the manner in which seizure activity spreads could lead to specifically-tailored therapies for epilepsy. We applied the electrical amygdala kindling model in two rhesus monkeys until these animals displayed consistent stage IV seizures. At this stage, we investigated the effective connectivity of the amygdala by means of electrical microstimulation during fMRI (EM-fMRI). In addition, we imaged changes in perfusion during a seizure using ictal SPECT perfusion imaging. The spatial overlap between the connectivity network and the ictal perfusion network was assessed both at the regional level, by calculating Dice coefficients using anatomically defined regions of interest, and at the voxel level. The kindled amygdala was extensively connected to bilateral cortical and subcortical structures, which in many cases were connected multisynaptically to the amygdala. At the regional level, the spatial extents of many of these fMRI activations and deactivations corresponded to the respective increases and decreases in perfusion imaged during a stage IV seizure. At the voxel level, however, some regions showed residual seizure-specific activity (not overlapping with the EM-fMRI activations) or fMRI-specific activation (not overlapping with the ictal SPECT activations), indicating that frequently, only a part of a region anatomically connected to the seizure onset zone participated in seizure propagation. Thus, EM-fMRI in the amygdala of electrically-kindled monkeys reveals widespread areas that are often connected multisynaptically to the seizure focus. Seizure activity appears to spread, to a large extent, via these connected areas. Elsevier 2016-06-01 /pmc/articles/PMC4959940/ /pubmed/27489773 http://dx.doi.org/10.1016/j.nicl.2016.05.020 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Regular Article Cleeren, Evy Premereur, Elsie Casteels, Cindy Goffin, Karolien Janssen, Peter Van Paesschen, Wim The effective connectivity of the seizure onset zone and ictal perfusion changes in amygdala kindled rhesus monkeys |
title | The effective connectivity of the seizure onset zone and ictal perfusion changes in amygdala kindled rhesus monkeys |
title_full | The effective connectivity of the seizure onset zone and ictal perfusion changes in amygdala kindled rhesus monkeys |
title_fullStr | The effective connectivity of the seizure onset zone and ictal perfusion changes in amygdala kindled rhesus monkeys |
title_full_unstemmed | The effective connectivity of the seizure onset zone and ictal perfusion changes in amygdala kindled rhesus monkeys |
title_short | The effective connectivity of the seizure onset zone and ictal perfusion changes in amygdala kindled rhesus monkeys |
title_sort | effective connectivity of the seizure onset zone and ictal perfusion changes in amygdala kindled rhesus monkeys |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4959940/ https://www.ncbi.nlm.nih.gov/pubmed/27489773 http://dx.doi.org/10.1016/j.nicl.2016.05.020 |
work_keys_str_mv | AT cleerenevy theeffectiveconnectivityoftheseizureonsetzoneandictalperfusionchangesinamygdalakindledrhesusmonkeys AT premereurelsie theeffectiveconnectivityoftheseizureonsetzoneandictalperfusionchangesinamygdalakindledrhesusmonkeys AT casteelscindy theeffectiveconnectivityoftheseizureonsetzoneandictalperfusionchangesinamygdalakindledrhesusmonkeys AT goffinkarolien theeffectiveconnectivityoftheseizureonsetzoneandictalperfusionchangesinamygdalakindledrhesusmonkeys AT janssenpeter theeffectiveconnectivityoftheseizureonsetzoneandictalperfusionchangesinamygdalakindledrhesusmonkeys AT vanpaesschenwim theeffectiveconnectivityoftheseizureonsetzoneandictalperfusionchangesinamygdalakindledrhesusmonkeys AT cleerenevy effectiveconnectivityoftheseizureonsetzoneandictalperfusionchangesinamygdalakindledrhesusmonkeys AT premereurelsie effectiveconnectivityoftheseizureonsetzoneandictalperfusionchangesinamygdalakindledrhesusmonkeys AT casteelscindy effectiveconnectivityoftheseizureonsetzoneandictalperfusionchangesinamygdalakindledrhesusmonkeys AT goffinkarolien effectiveconnectivityoftheseizureonsetzoneandictalperfusionchangesinamygdalakindledrhesusmonkeys AT janssenpeter effectiveconnectivityoftheseizureonsetzoneandictalperfusionchangesinamygdalakindledrhesusmonkeys AT vanpaesschenwim effectiveconnectivityoftheseizureonsetzoneandictalperfusionchangesinamygdalakindledrhesusmonkeys |