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Acute effect of antiseizure drugs on background oscillations in Scn1a (A1783V) Dravet syndrome mouse model

Dravet syndrome (Dravet) is a rare and severe form of developmental epileptic encephalopathy. Antiseizure medications (ASMs) for Dravet patients include valproic acid (VA) or clobazam (CLB), with or without stiripentol (STP), while sodium channel blockers like carbamazepine (CBZ) or lamotrigine (LTG...

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Autores principales: Quinn, Shir, Brusel, Marina, Ovadia, Mor, Rubinstein, Moran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10067575/
https://www.ncbi.nlm.nih.gov/pubmed/37021051
http://dx.doi.org/10.3389/fphar.2023.1118216
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author Quinn, Shir
Brusel, Marina
Ovadia, Mor
Rubinstein, Moran
author_facet Quinn, Shir
Brusel, Marina
Ovadia, Mor
Rubinstein, Moran
author_sort Quinn, Shir
collection PubMed
description Dravet syndrome (Dravet) is a rare and severe form of developmental epileptic encephalopathy. Antiseizure medications (ASMs) for Dravet patients include valproic acid (VA) or clobazam (CLB), with or without stiripentol (STP), while sodium channel blockers like carbamazepine (CBZ) or lamotrigine (LTG) are contraindicated. In addition to their effect on epileptic phenotypes, ASMs were shown to modify the properties of background neuronal activity. Nevertheless, little is known about these background properties alterations in Dravet. Here, utilizing Dravet mice (DS, Scn1a (A1783V/WT)), we tested the acute effect of several ASMs on background electrocorticography (ECoG) activity and frequency of interictal spikes. Compared to wild-type mice, background ECoG activity in DS mice had lower power and reduced phase coherence, which was not corrected by any of the tested ASMs. However, acute administration of Dravet-recommended drugs, VA, CLB, or a combination of CLB + STP, caused, in most mice, a reduction in the frequency of interictal spikes, alongside an increase in the relative contribution of the beta frequency band. Conversely, CBZ and LTG increased the frequency of interictal spikes, with no effect on background spectral properties. Moreover, we uncovered a correlation between the reduction in interictal spike frequency, the drug-induced effect on the power of background activity, and a spectral shift toward higher frequency bands. Together, these data provide a comprehensive analysis of the effect of selected ASMs on the properties of background neuronal oscillations, and highlight a possible correlation between their effect on epilepsy and background activity.
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spelling pubmed-100675752023-04-04 Acute effect of antiseizure drugs on background oscillations in Scn1a (A1783V) Dravet syndrome mouse model Quinn, Shir Brusel, Marina Ovadia, Mor Rubinstein, Moran Front Pharmacol Pharmacology Dravet syndrome (Dravet) is a rare and severe form of developmental epileptic encephalopathy. Antiseizure medications (ASMs) for Dravet patients include valproic acid (VA) or clobazam (CLB), with or without stiripentol (STP), while sodium channel blockers like carbamazepine (CBZ) or lamotrigine (LTG) are contraindicated. In addition to their effect on epileptic phenotypes, ASMs were shown to modify the properties of background neuronal activity. Nevertheless, little is known about these background properties alterations in Dravet. Here, utilizing Dravet mice (DS, Scn1a (A1783V/WT)), we tested the acute effect of several ASMs on background electrocorticography (ECoG) activity and frequency of interictal spikes. Compared to wild-type mice, background ECoG activity in DS mice had lower power and reduced phase coherence, which was not corrected by any of the tested ASMs. However, acute administration of Dravet-recommended drugs, VA, CLB, or a combination of CLB + STP, caused, in most mice, a reduction in the frequency of interictal spikes, alongside an increase in the relative contribution of the beta frequency band. Conversely, CBZ and LTG increased the frequency of interictal spikes, with no effect on background spectral properties. Moreover, we uncovered a correlation between the reduction in interictal spike frequency, the drug-induced effect on the power of background activity, and a spectral shift toward higher frequency bands. Together, these data provide a comprehensive analysis of the effect of selected ASMs on the properties of background neuronal oscillations, and highlight a possible correlation between their effect on epilepsy and background activity. Frontiers Media S.A. 2023-03-20 /pmc/articles/PMC10067575/ /pubmed/37021051 http://dx.doi.org/10.3389/fphar.2023.1118216 Text en Copyright © 2023 Quinn, Brusel, Ovadia and Rubinstein. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Quinn, Shir
Brusel, Marina
Ovadia, Mor
Rubinstein, Moran
Acute effect of antiseizure drugs on background oscillations in Scn1a (A1783V) Dravet syndrome mouse model
title Acute effect of antiseizure drugs on background oscillations in Scn1a (A1783V) Dravet syndrome mouse model
title_full Acute effect of antiseizure drugs on background oscillations in Scn1a (A1783V) Dravet syndrome mouse model
title_fullStr Acute effect of antiseizure drugs on background oscillations in Scn1a (A1783V) Dravet syndrome mouse model
title_full_unstemmed Acute effect of antiseizure drugs on background oscillations in Scn1a (A1783V) Dravet syndrome mouse model
title_short Acute effect of antiseizure drugs on background oscillations in Scn1a (A1783V) Dravet syndrome mouse model
title_sort acute effect of antiseizure drugs on background oscillations in scn1a (a1783v) dravet syndrome mouse model
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10067575/
https://www.ncbi.nlm.nih.gov/pubmed/37021051
http://dx.doi.org/10.3389/fphar.2023.1118216
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