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Temporal Coordination of Hippocampal Neurons Reflects Cognitive Outcome Post-febrile Status Epilepticus()()
The coordination of dynamic neural activity within and between neural networks is believed to underlie normal cognitive processes. Conversely, cognitive deficits that occur following neurological insults may result from network discoordination. We hypothesized that cognitive outcome following febril...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4909381/ https://www.ncbi.nlm.nih.gov/pubmed/27322471 http://dx.doi.org/10.1016/j.ebiom.2016.03.039 |
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author | Barry, Jeremy M. Sakkaki, Sophie Barriere, Sylvain J. Patterson, Katelin P. Lenck-Santini, Pierre Pascal Scott, Rod C. Baram, Tallie Z. Holmes, Gregory L. |
author_facet | Barry, Jeremy M. Sakkaki, Sophie Barriere, Sylvain J. Patterson, Katelin P. Lenck-Santini, Pierre Pascal Scott, Rod C. Baram, Tallie Z. Holmes, Gregory L. |
author_sort | Barry, Jeremy M. |
collection | PubMed |
description | The coordination of dynamic neural activity within and between neural networks is believed to underlie normal cognitive processes. Conversely, cognitive deficits that occur following neurological insults may result from network discoordination. We hypothesized that cognitive outcome following febrile status epilepticus (FSE) depends on network efficacy within and between fields CA1 and CA3 to dynamically organize cell activity by theta phase. Control and FSE rats were trained to forage or perform an active avoidance spatial task. FSE rats were sorted by those that were able to reach task criterion (FSE-L) and those that could not (FSE-NL). FSE-NL CA1 place cells did not exhibit phase preference in either context and exhibited poor cross-theta interaction between CA1 and CA3. FSE-L and control CA1 place cells exhibited phase preference at peak theta that shifted during active avoidance to the same static phase preference observed in CA3. Temporal coordination of neuronal activity by theta phase may therefore explain variability in cognitive outcome following neurological insults in early development. |
format | Online Article Text |
id | pubmed-4909381 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-49093812016-06-21 Temporal Coordination of Hippocampal Neurons Reflects Cognitive Outcome Post-febrile Status Epilepticus()() Barry, Jeremy M. Sakkaki, Sophie Barriere, Sylvain J. Patterson, Katelin P. Lenck-Santini, Pierre Pascal Scott, Rod C. Baram, Tallie Z. Holmes, Gregory L. EBioMedicine Research Paper The coordination of dynamic neural activity within and between neural networks is believed to underlie normal cognitive processes. Conversely, cognitive deficits that occur following neurological insults may result from network discoordination. We hypothesized that cognitive outcome following febrile status epilepticus (FSE) depends on network efficacy within and between fields CA1 and CA3 to dynamically organize cell activity by theta phase. Control and FSE rats were trained to forage or perform an active avoidance spatial task. FSE rats were sorted by those that were able to reach task criterion (FSE-L) and those that could not (FSE-NL). FSE-NL CA1 place cells did not exhibit phase preference in either context and exhibited poor cross-theta interaction between CA1 and CA3. FSE-L and control CA1 place cells exhibited phase preference at peak theta that shifted during active avoidance to the same static phase preference observed in CA3. Temporal coordination of neuronal activity by theta phase may therefore explain variability in cognitive outcome following neurological insults in early development. Elsevier 2016-04-06 /pmc/articles/PMC4909381/ /pubmed/27322471 http://dx.doi.org/10.1016/j.ebiom.2016.03.039 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Paper Barry, Jeremy M. Sakkaki, Sophie Barriere, Sylvain J. Patterson, Katelin P. Lenck-Santini, Pierre Pascal Scott, Rod C. Baram, Tallie Z. Holmes, Gregory L. Temporal Coordination of Hippocampal Neurons Reflects Cognitive Outcome Post-febrile Status Epilepticus()() |
title | Temporal Coordination of Hippocampal Neurons Reflects Cognitive Outcome Post-febrile Status Epilepticus()() |
title_full | Temporal Coordination of Hippocampal Neurons Reflects Cognitive Outcome Post-febrile Status Epilepticus()() |
title_fullStr | Temporal Coordination of Hippocampal Neurons Reflects Cognitive Outcome Post-febrile Status Epilepticus()() |
title_full_unstemmed | Temporal Coordination of Hippocampal Neurons Reflects Cognitive Outcome Post-febrile Status Epilepticus()() |
title_short | Temporal Coordination of Hippocampal Neurons Reflects Cognitive Outcome Post-febrile Status Epilepticus()() |
title_sort | temporal coordination of hippocampal neurons reflects cognitive outcome post-febrile status epilepticus()() |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4909381/ https://www.ncbi.nlm.nih.gov/pubmed/27322471 http://dx.doi.org/10.1016/j.ebiom.2016.03.039 |
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