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Altered Oscillatory Dynamics of CA1 Parvalbumin Basket Cells during Theta–Gamma Rhythmopathies of Temporal Lobe Epilepsy

Recent reports in human demonstrate a role of theta–gamma coupling in memory for spatial episodes and a lack of coupling in people experiencing temporal lobe epilepsy, but the mechanisms are unknown. Using multisite silicon probe recordings of epileptic rats engaged in episodic-like object recogniti...

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Autores principales: Lopez-Pigozzi, Diego, Laurent, François, Brotons-Mas, Jorge R., Valderrama, Mario, Valero, Manuel, Fernandez-Lamo, Ivan, Cid, Elena, Gomez-Dominguez, Daniel, Gal, Beatriz, Menendez de la Prida, Liset
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5114702/
https://www.ncbi.nlm.nih.gov/pubmed/27896315
http://dx.doi.org/10.1523/ENEURO.0284-16.2016
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author Lopez-Pigozzi, Diego
Laurent, François
Brotons-Mas, Jorge R.
Valderrama, Mario
Valero, Manuel
Fernandez-Lamo, Ivan
Cid, Elena
Gomez-Dominguez, Daniel
Gal, Beatriz
Menendez de la Prida, Liset
author_facet Lopez-Pigozzi, Diego
Laurent, François
Brotons-Mas, Jorge R.
Valderrama, Mario
Valero, Manuel
Fernandez-Lamo, Ivan
Cid, Elena
Gomez-Dominguez, Daniel
Gal, Beatriz
Menendez de la Prida, Liset
author_sort Lopez-Pigozzi, Diego
collection PubMed
description Recent reports in human demonstrate a role of theta–gamma coupling in memory for spatial episodes and a lack of coupling in people experiencing temporal lobe epilepsy, but the mechanisms are unknown. Using multisite silicon probe recordings of epileptic rats engaged in episodic-like object recognition tasks, we sought to evaluate the role of theta–gamma coupling in the absence of epileptiform activities. Our data reveal a specific association between theta–gamma (30–60 Hz) coupling at the proximal stratum radiatum of CA1 and spatial memory deficits. We targeted the microcircuit mechanisms with a novel approach to identify putative interneuronal types in tetrode recordings (parvalbumin basket cells in particular) and validated classification criteria in the epileptic context with neurochemical identification of intracellularly recorded cells. In epileptic rats, putative parvalbumin basket cells fired poorly modulated at the falling theta phase, consistent with weaker inputs from Schaffer collaterals and attenuated gamma oscillations, as evaluated by theta-phase decomposition of current–source density signals. We propose that theta–gamma interneuronal rhythmopathies of the temporal lobe are intimately related to episodic memory dysfunction in this condition.
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spelling pubmed-51147022016-11-28 Altered Oscillatory Dynamics of CA1 Parvalbumin Basket Cells during Theta–Gamma Rhythmopathies of Temporal Lobe Epilepsy Lopez-Pigozzi, Diego Laurent, François Brotons-Mas, Jorge R. Valderrama, Mario Valero, Manuel Fernandez-Lamo, Ivan Cid, Elena Gomez-Dominguez, Daniel Gal, Beatriz Menendez de la Prida, Liset eNeuro New Research Recent reports in human demonstrate a role of theta–gamma coupling in memory for spatial episodes and a lack of coupling in people experiencing temporal lobe epilepsy, but the mechanisms are unknown. Using multisite silicon probe recordings of epileptic rats engaged in episodic-like object recognition tasks, we sought to evaluate the role of theta–gamma coupling in the absence of epileptiform activities. Our data reveal a specific association between theta–gamma (30–60 Hz) coupling at the proximal stratum radiatum of CA1 and spatial memory deficits. We targeted the microcircuit mechanisms with a novel approach to identify putative interneuronal types in tetrode recordings (parvalbumin basket cells in particular) and validated classification criteria in the epileptic context with neurochemical identification of intracellularly recorded cells. In epileptic rats, putative parvalbumin basket cells fired poorly modulated at the falling theta phase, consistent with weaker inputs from Schaffer collaterals and attenuated gamma oscillations, as evaluated by theta-phase decomposition of current–source density signals. We propose that theta–gamma interneuronal rhythmopathies of the temporal lobe are intimately related to episodic memory dysfunction in this condition. Society for Neuroscience 2016-11-18 /pmc/articles/PMC5114702/ /pubmed/27896315 http://dx.doi.org/10.1523/ENEURO.0284-16.2016 Text en Copyright © 2016 Lopez-Pigozzi et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle New Research
Lopez-Pigozzi, Diego
Laurent, François
Brotons-Mas, Jorge R.
Valderrama, Mario
Valero, Manuel
Fernandez-Lamo, Ivan
Cid, Elena
Gomez-Dominguez, Daniel
Gal, Beatriz
Menendez de la Prida, Liset
Altered Oscillatory Dynamics of CA1 Parvalbumin Basket Cells during Theta–Gamma Rhythmopathies of Temporal Lobe Epilepsy
title Altered Oscillatory Dynamics of CA1 Parvalbumin Basket Cells during Theta–Gamma Rhythmopathies of Temporal Lobe Epilepsy
title_full Altered Oscillatory Dynamics of CA1 Parvalbumin Basket Cells during Theta–Gamma Rhythmopathies of Temporal Lobe Epilepsy
title_fullStr Altered Oscillatory Dynamics of CA1 Parvalbumin Basket Cells during Theta–Gamma Rhythmopathies of Temporal Lobe Epilepsy
title_full_unstemmed Altered Oscillatory Dynamics of CA1 Parvalbumin Basket Cells during Theta–Gamma Rhythmopathies of Temporal Lobe Epilepsy
title_short Altered Oscillatory Dynamics of CA1 Parvalbumin Basket Cells during Theta–Gamma Rhythmopathies of Temporal Lobe Epilepsy
title_sort altered oscillatory dynamics of ca1 parvalbumin basket cells during theta–gamma rhythmopathies of temporal lobe epilepsy
topic New Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5114702/
https://www.ncbi.nlm.nih.gov/pubmed/27896315
http://dx.doi.org/10.1523/ENEURO.0284-16.2016
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