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From sleep spindles of natural sleep to spike and wave discharges of typical absence seizures: is the hypothesis still valid?

The temporal coincidence of sleep spindles and spike-and-wave discharges (SWDs) in patients with idiopathic generalized epilepsies, together with the transformation of spindles into SWDs following intramuscular injection of the weak GABAA receptor (GABAAR) antagonist, penicillin, in an experimental...

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Detalles Bibliográficos
Autores principales: Leresche, Nathalie, Lambert, Régis C., Errington, Adam C., Crunelli, Vincenzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3256322/
https://www.ncbi.nlm.nih.gov/pubmed/21861061
http://dx.doi.org/10.1007/s00424-011-1009-3
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author Leresche, Nathalie
Lambert, Régis C.
Errington, Adam C.
Crunelli, Vincenzo
author_facet Leresche, Nathalie
Lambert, Régis C.
Errington, Adam C.
Crunelli, Vincenzo
author_sort Leresche, Nathalie
collection PubMed
description The temporal coincidence of sleep spindles and spike-and-wave discharges (SWDs) in patients with idiopathic generalized epilepsies, together with the transformation of spindles into SWDs following intramuscular injection of the weak GABAA receptor (GABAAR) antagonist, penicillin, in an experimental model, brought about the view that SWDs may represent ‘perverted’ sleep spindles. Over the last 20 years, this hypothesis has received considerable support, in particular by in vitro studies of thalamic oscillations following pharmacological/genetic manipulations of GABAARs. However, from a critical appraisal of the evidence in absence epilepsy patients and well-established models of absence epilepsy it emerges that SWDs can occur as frequently during wakefulness as during sleep, with their preferential occurrence in either one of these behavioural states often being patient dependent. Moreover, whereas the EEG expression of both SWDs and sleep spindles requires the integrity of the entire cortico-thalamo-cortical network, SWDs initiates in cortex while sleep spindles in thalamus. Furthermore, the hypothesis of a reduction in GABAAR function across the entire cortico-thalamo-cortical network as the basis for the transformation of sleep spindles into SWDs is no longer tenable. In fact, while a decreased GABAAR function may be present in some cortical layers and in the reticular thalamic nucleus, both phasic and tonic GABAAR inhibitions of thalamo-cortical neurons are either unchanged or increased in this epileptic phenotype. In summary, these differences between SWDs and sleep spindles question the view that the EEG hallmark of absence seizures results from a transformation of this EEG oscillation of natural sleep.
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spelling pubmed-32563222012-01-23 From sleep spindles of natural sleep to spike and wave discharges of typical absence seizures: is the hypothesis still valid? Leresche, Nathalie Lambert, Régis C. Errington, Adam C. Crunelli, Vincenzo Pflugers Arch Invited Review The temporal coincidence of sleep spindles and spike-and-wave discharges (SWDs) in patients with idiopathic generalized epilepsies, together with the transformation of spindles into SWDs following intramuscular injection of the weak GABAA receptor (GABAAR) antagonist, penicillin, in an experimental model, brought about the view that SWDs may represent ‘perverted’ sleep spindles. Over the last 20 years, this hypothesis has received considerable support, in particular by in vitro studies of thalamic oscillations following pharmacological/genetic manipulations of GABAARs. However, from a critical appraisal of the evidence in absence epilepsy patients and well-established models of absence epilepsy it emerges that SWDs can occur as frequently during wakefulness as during sleep, with their preferential occurrence in either one of these behavioural states often being patient dependent. Moreover, whereas the EEG expression of both SWDs and sleep spindles requires the integrity of the entire cortico-thalamo-cortical network, SWDs initiates in cortex while sleep spindles in thalamus. Furthermore, the hypothesis of a reduction in GABAAR function across the entire cortico-thalamo-cortical network as the basis for the transformation of sleep spindles into SWDs is no longer tenable. In fact, while a decreased GABAAR function may be present in some cortical layers and in the reticular thalamic nucleus, both phasic and tonic GABAAR inhibitions of thalamo-cortical neurons are either unchanged or increased in this epileptic phenotype. In summary, these differences between SWDs and sleep spindles question the view that the EEG hallmark of absence seizures results from a transformation of this EEG oscillation of natural sleep. Springer-Verlag 2011-08-23 2012-01 /pmc/articles/PMC3256322/ /pubmed/21861061 http://dx.doi.org/10.1007/s00424-011-1009-3 Text en © Springer-Verlag 2011
spellingShingle Invited Review
Leresche, Nathalie
Lambert, Régis C.
Errington, Adam C.
Crunelli, Vincenzo
From sleep spindles of natural sleep to spike and wave discharges of typical absence seizures: is the hypothesis still valid?
title From sleep spindles of natural sleep to spike and wave discharges of typical absence seizures: is the hypothesis still valid?
title_full From sleep spindles of natural sleep to spike and wave discharges of typical absence seizures: is the hypothesis still valid?
title_fullStr From sleep spindles of natural sleep to spike and wave discharges of typical absence seizures: is the hypothesis still valid?
title_full_unstemmed From sleep spindles of natural sleep to spike and wave discharges of typical absence seizures: is the hypothesis still valid?
title_short From sleep spindles of natural sleep to spike and wave discharges of typical absence seizures: is the hypothesis still valid?
title_sort from sleep spindles of natural sleep to spike and wave discharges of typical absence seizures: is the hypothesis still valid?
topic Invited Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3256322/
https://www.ncbi.nlm.nih.gov/pubmed/21861061
http://dx.doi.org/10.1007/s00424-011-1009-3
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