Cargando…
Amygdala Low-Frequency Stimulation Reduces Pathological Phase-Amplitude Coupling in the Pilocarpine Model of Epilepsy
Temporal-lobe epilepsy (TLE) is the most common type of drug-resistant epilepsy and warrants the development of new therapies, such as deep-brain stimulation (DBS). DBS was applied to different brain regions for patients with epilepsy; however, the mechanisms of action are not fully understood. Ther...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7696538/ https://www.ncbi.nlm.nih.gov/pubmed/33202818 http://dx.doi.org/10.3390/brainsci10110856 |
_version_ | 1783615427697442816 |
---|---|
author | Mihály, István Orbán-Kis, Károly Gáll, Zsolt Berki, Ádám-József Bod, Réka-Barbara Szilágyi, Tibor |
author_facet | Mihály, István Orbán-Kis, Károly Gáll, Zsolt Berki, Ádám-József Bod, Réka-Barbara Szilágyi, Tibor |
author_sort | Mihály, István |
collection | PubMed |
description | Temporal-lobe epilepsy (TLE) is the most common type of drug-resistant epilepsy and warrants the development of new therapies, such as deep-brain stimulation (DBS). DBS was applied to different brain regions for patients with epilepsy; however, the mechanisms of action are not fully understood. Therefore, we tried to characterize the effect of amygdala DBS on hippocampal electrical activity in the lithium-pilocarpine model in male Wistar rats. After status epilepticus (SE) induction, seizure patterns were determined based on continuous video recordings. Recording electrodes were inserted in the left and right hippocampus and a stimulating electrode in the left basolateral amygdala of both Pilo and age-matched control rats 10 weeks after SE. Daily stimulation protocol consisted of 4 × 50 s stimulation trains (4-Hz, regular interpulse interval) for 10 days. The hippocampal electroencephalogram was analyzed offline: interictal epileptiform discharge (IED) frequency, spectral analysis, and phase-amplitude coupling (PAC) between delta band and higher frequencies were measured. We found that the seizure rate and duration decreased (by 23% and 26.5%) and the decrease in seizure rate correlated negatively with the IED frequency. PAC was elevated in epileptic animals and DBS reduced the pathologically increased PAC and increased the average theta power (25.9% ± 1.1 vs. 30.3% ± 1.1; p < 0.01). Increasing theta power and reducing the PAC could be two possible mechanisms by which DBS may exhibit its antiepileptic effect in TLE; moreover, they could be used to monitor effectiveness of stimulation. |
format | Online Article Text |
id | pubmed-7696538 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-76965382020-11-29 Amygdala Low-Frequency Stimulation Reduces Pathological Phase-Amplitude Coupling in the Pilocarpine Model of Epilepsy Mihály, István Orbán-Kis, Károly Gáll, Zsolt Berki, Ádám-József Bod, Réka-Barbara Szilágyi, Tibor Brain Sci Article Temporal-lobe epilepsy (TLE) is the most common type of drug-resistant epilepsy and warrants the development of new therapies, such as deep-brain stimulation (DBS). DBS was applied to different brain regions for patients with epilepsy; however, the mechanisms of action are not fully understood. Therefore, we tried to characterize the effect of amygdala DBS on hippocampal electrical activity in the lithium-pilocarpine model in male Wistar rats. After status epilepticus (SE) induction, seizure patterns were determined based on continuous video recordings. Recording electrodes were inserted in the left and right hippocampus and a stimulating electrode in the left basolateral amygdala of both Pilo and age-matched control rats 10 weeks after SE. Daily stimulation protocol consisted of 4 × 50 s stimulation trains (4-Hz, regular interpulse interval) for 10 days. The hippocampal electroencephalogram was analyzed offline: interictal epileptiform discharge (IED) frequency, spectral analysis, and phase-amplitude coupling (PAC) between delta band and higher frequencies were measured. We found that the seizure rate and duration decreased (by 23% and 26.5%) and the decrease in seizure rate correlated negatively with the IED frequency. PAC was elevated in epileptic animals and DBS reduced the pathologically increased PAC and increased the average theta power (25.9% ± 1.1 vs. 30.3% ± 1.1; p < 0.01). Increasing theta power and reducing the PAC could be two possible mechanisms by which DBS may exhibit its antiepileptic effect in TLE; moreover, they could be used to monitor effectiveness of stimulation. MDPI 2020-11-13 /pmc/articles/PMC7696538/ /pubmed/33202818 http://dx.doi.org/10.3390/brainsci10110856 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Mihály, István Orbán-Kis, Károly Gáll, Zsolt Berki, Ádám-József Bod, Réka-Barbara Szilágyi, Tibor Amygdala Low-Frequency Stimulation Reduces Pathological Phase-Amplitude Coupling in the Pilocarpine Model of Epilepsy |
title | Amygdala Low-Frequency Stimulation Reduces Pathological Phase-Amplitude Coupling in the Pilocarpine Model of Epilepsy |
title_full | Amygdala Low-Frequency Stimulation Reduces Pathological Phase-Amplitude Coupling in the Pilocarpine Model of Epilepsy |
title_fullStr | Amygdala Low-Frequency Stimulation Reduces Pathological Phase-Amplitude Coupling in the Pilocarpine Model of Epilepsy |
title_full_unstemmed | Amygdala Low-Frequency Stimulation Reduces Pathological Phase-Amplitude Coupling in the Pilocarpine Model of Epilepsy |
title_short | Amygdala Low-Frequency Stimulation Reduces Pathological Phase-Amplitude Coupling in the Pilocarpine Model of Epilepsy |
title_sort | amygdala low-frequency stimulation reduces pathological phase-amplitude coupling in the pilocarpine model of epilepsy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7696538/ https://www.ncbi.nlm.nih.gov/pubmed/33202818 http://dx.doi.org/10.3390/brainsci10110856 |
work_keys_str_mv | AT mihalyistvan amygdalalowfrequencystimulationreducespathologicalphaseamplitudecouplinginthepilocarpinemodelofepilepsy AT orbankiskaroly amygdalalowfrequencystimulationreducespathologicalphaseamplitudecouplinginthepilocarpinemodelofepilepsy AT gallzsolt amygdalalowfrequencystimulationreducespathologicalphaseamplitudecouplinginthepilocarpinemodelofepilepsy AT berkiadamjozsef amygdalalowfrequencystimulationreducespathologicalphaseamplitudecouplinginthepilocarpinemodelofepilepsy AT bodrekabarbara amygdalalowfrequencystimulationreducespathologicalphaseamplitudecouplinginthepilocarpinemodelofepilepsy AT szilagyitibor amygdalalowfrequencystimulationreducespathologicalphaseamplitudecouplinginthepilocarpinemodelofepilepsy |