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BMAL1 controls the diurnal rhythm and set point for electrical seizure threshold in mice

The epilepsies are a heterogeneous group of neurological diseases defined by the occurrence of unprovoked seizures which, in many cases, are correlated with diurnal rhythms. In order to gain insight into the biological mechanisms controlling this phenomenon, we characterized time-of-day effects on e...

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Autores principales: Gerstner, Jason R., Smith, George G., Lenz, Olivia, Perron, Isaac J., Buono, Russell J., Ferraro, Thomas N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4071977/
https://www.ncbi.nlm.nih.gov/pubmed/25018707
http://dx.doi.org/10.3389/fnsys.2014.00121
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author Gerstner, Jason R.
Smith, George G.
Lenz, Olivia
Perron, Isaac J.
Buono, Russell J.
Ferraro, Thomas N.
author_facet Gerstner, Jason R.
Smith, George G.
Lenz, Olivia
Perron, Isaac J.
Buono, Russell J.
Ferraro, Thomas N.
author_sort Gerstner, Jason R.
collection PubMed
description The epilepsies are a heterogeneous group of neurological diseases defined by the occurrence of unprovoked seizures which, in many cases, are correlated with diurnal rhythms. In order to gain insight into the biological mechanisms controlling this phenomenon, we characterized time-of-day effects on electrical seizure threshold in mice. Male C57BL/6J wild-type mice were maintained on a 14/10 h light/dark cycle, from birth until 6 weeks of age for seizure testing. Seizure thresholds were measured using a step-wise paradigm involving a single daily electrical stimulus. Results showed that the current required to elicit both generalized and maximal seizures was significantly higher in mice tested during the dark phase of the diurnal cycle compared to mice tested during the light phase. This rhythm was absent in BMAL1 knockout (KO) mice. BMAL1 KO also exhibited significantly reduced seizure thresholds at all times tested, compared to C57BL/6J mice. Results document a significant influence of time-of-day on electrical seizure threshold in mice and suggest that this effect is under the control of genes that are known to regulate circadian behaviors. Furthermore, low seizure thresholds in BMAL1 KO mice suggest that BMAL1 itself is directly involved in controlling neuronal excitability.
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spelling pubmed-40719772014-07-11 BMAL1 controls the diurnal rhythm and set point for electrical seizure threshold in mice Gerstner, Jason R. Smith, George G. Lenz, Olivia Perron, Isaac J. Buono, Russell J. Ferraro, Thomas N. Front Syst Neurosci Neuroscience The epilepsies are a heterogeneous group of neurological diseases defined by the occurrence of unprovoked seizures which, in many cases, are correlated with diurnal rhythms. In order to gain insight into the biological mechanisms controlling this phenomenon, we characterized time-of-day effects on electrical seizure threshold in mice. Male C57BL/6J wild-type mice were maintained on a 14/10 h light/dark cycle, from birth until 6 weeks of age for seizure testing. Seizure thresholds were measured using a step-wise paradigm involving a single daily electrical stimulus. Results showed that the current required to elicit both generalized and maximal seizures was significantly higher in mice tested during the dark phase of the diurnal cycle compared to mice tested during the light phase. This rhythm was absent in BMAL1 knockout (KO) mice. BMAL1 KO also exhibited significantly reduced seizure thresholds at all times tested, compared to C57BL/6J mice. Results document a significant influence of time-of-day on electrical seizure threshold in mice and suggest that this effect is under the control of genes that are known to regulate circadian behaviors. Furthermore, low seizure thresholds in BMAL1 KO mice suggest that BMAL1 itself is directly involved in controlling neuronal excitability. Frontiers Media S.A. 2014-06-26 /pmc/articles/PMC4071977/ /pubmed/25018707 http://dx.doi.org/10.3389/fnsys.2014.00121 Text en Copyright © 2014 Gerstner, Smith, Lenz, Perron, Buono and Ferraro. http://creativecommons.org/licenses/by/3.0/ 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) or licensor 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 Neuroscience
Gerstner, Jason R.
Smith, George G.
Lenz, Olivia
Perron, Isaac J.
Buono, Russell J.
Ferraro, Thomas N.
BMAL1 controls the diurnal rhythm and set point for electrical seizure threshold in mice
title BMAL1 controls the diurnal rhythm and set point for electrical seizure threshold in mice
title_full BMAL1 controls the diurnal rhythm and set point for electrical seizure threshold in mice
title_fullStr BMAL1 controls the diurnal rhythm and set point for electrical seizure threshold in mice
title_full_unstemmed BMAL1 controls the diurnal rhythm and set point for electrical seizure threshold in mice
title_short BMAL1 controls the diurnal rhythm and set point for electrical seizure threshold in mice
title_sort bmal1 controls the diurnal rhythm and set point for electrical seizure threshold in mice
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4071977/
https://www.ncbi.nlm.nih.gov/pubmed/25018707
http://dx.doi.org/10.3389/fnsys.2014.00121
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