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Loss of Circadian Timing Disrupts Theta Episodes during Object Exploration
This study examined whether theta oscillations were compromised by the type of circadian disruption that impairs hippocampal-dependent memory processes. In prior studies on Siberian hamsters, we developed a one-time light treatment that eliminated circadian timing in the central pacemaker, the supra...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7711584/ https://www.ncbi.nlm.nih.gov/pubmed/33271811 http://dx.doi.org/10.3390/clockssleep2040038 |
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author | Loewke, Adrienne C. Garrett, Alex Steiger, Athreya Fisher, Nathan Heller, H. Craig Colas, Damien Ruby, Norman F. |
author_facet | Loewke, Adrienne C. Garrett, Alex Steiger, Athreya Fisher, Nathan Heller, H. Craig Colas, Damien Ruby, Norman F. |
author_sort | Loewke, Adrienne C. |
collection | PubMed |
description | This study examined whether theta oscillations were compromised by the type of circadian disruption that impairs hippocampal-dependent memory processes. In prior studies on Siberian hamsters, we developed a one-time light treatment that eliminated circadian timing in the central pacemaker, the suprachiasmatic nucleus (SCN). These arrhythmic animals had impaired hippocampal-dependent memory whereas animals made arrhythmic with SCN lesions did not. The current study examined whether theta oscillations are compromised by the same light treatment that produced memory impairments in these animals. We found that both methods of inducing circadian-arrhythmia shortened theta episodes in the EEG by nearly 50%. SCN-lesioned animals, however, exhibited a 3-fold increase in the number of theta episodes and more than doubled the total time that theta dominated the EEG compared to SCN-intact circadian-arrhythmic animals. Video tracking showed that changes in theta were paralleled by similar changes in exploration behavior. These results suggest that the circadian-arrhythmic SCN interferes with hippocampal memory encoding by fragmenting theta oscillations. SCN-lesioned animals can, however, compensate for the shortened theta episodes by increasing their frequency. Implications for rhythm coherence and theta sequence models of memory formation are discussed. |
format | Online Article Text |
id | pubmed-7711584 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77115842020-12-04 Loss of Circadian Timing Disrupts Theta Episodes during Object Exploration Loewke, Adrienne C. Garrett, Alex Steiger, Athreya Fisher, Nathan Heller, H. Craig Colas, Damien Ruby, Norman F. Clocks Sleep Article This study examined whether theta oscillations were compromised by the type of circadian disruption that impairs hippocampal-dependent memory processes. In prior studies on Siberian hamsters, we developed a one-time light treatment that eliminated circadian timing in the central pacemaker, the suprachiasmatic nucleus (SCN). These arrhythmic animals had impaired hippocampal-dependent memory whereas animals made arrhythmic with SCN lesions did not. The current study examined whether theta oscillations are compromised by the same light treatment that produced memory impairments in these animals. We found that both methods of inducing circadian-arrhythmia shortened theta episodes in the EEG by nearly 50%. SCN-lesioned animals, however, exhibited a 3-fold increase in the number of theta episodes and more than doubled the total time that theta dominated the EEG compared to SCN-intact circadian-arrhythmic animals. Video tracking showed that changes in theta were paralleled by similar changes in exploration behavior. These results suggest that the circadian-arrhythmic SCN interferes with hippocampal memory encoding by fragmenting theta oscillations. SCN-lesioned animals can, however, compensate for the shortened theta episodes by increasing their frequency. Implications for rhythm coherence and theta sequence models of memory formation are discussed. MDPI 2020-12-01 /pmc/articles/PMC7711584/ /pubmed/33271811 http://dx.doi.org/10.3390/clockssleep2040038 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Loewke, Adrienne C. Garrett, Alex Steiger, Athreya Fisher, Nathan Heller, H. Craig Colas, Damien Ruby, Norman F. Loss of Circadian Timing Disrupts Theta Episodes during Object Exploration |
title | Loss of Circadian Timing Disrupts Theta Episodes during Object Exploration |
title_full | Loss of Circadian Timing Disrupts Theta Episodes during Object Exploration |
title_fullStr | Loss of Circadian Timing Disrupts Theta Episodes during Object Exploration |
title_full_unstemmed | Loss of Circadian Timing Disrupts Theta Episodes during Object Exploration |
title_short | Loss of Circadian Timing Disrupts Theta Episodes during Object Exploration |
title_sort | loss of circadian timing disrupts theta episodes during object exploration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7711584/ https://www.ncbi.nlm.nih.gov/pubmed/33271811 http://dx.doi.org/10.3390/clockssleep2040038 |
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