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Sleep loss diminishes hippocampal reactivation and replay

Memories benefit from sleep, and sleep loss immediately following learning has a negative impact on subsequent memory storage. Several prominent hypotheses ascribe a central role to hippocampal sharp-wave ripples (SWRs), and the concurrent reactivation and replay of neuronal patterns from waking exp...

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Autores principales: Giri, Bapun, Kaya, Utku, Maboudi, Kourosh, Abel, Ted, Diba, Kamran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Journal Experts 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9949250/
https://www.ncbi.nlm.nih.gov/pubmed/36824950
http://dx.doi.org/10.21203/rs.3.rs-2540186/v1
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author Giri, Bapun
Kaya, Utku
Maboudi, Kourosh
Abel, Ted
Diba, Kamran
author_facet Giri, Bapun
Kaya, Utku
Maboudi, Kourosh
Abel, Ted
Diba, Kamran
author_sort Giri, Bapun
collection PubMed
description Memories benefit from sleep, and sleep loss immediately following learning has a negative impact on subsequent memory storage. Several prominent hypotheses ascribe a central role to hippocampal sharp-wave ripples (SWRs), and the concurrent reactivation and replay of neuronal patterns from waking experience, in the offline memory consolidation process that occurs during sleep. However, little is known about how SWRs, reactivation, and replay are affected when animals are subjected to sleep deprivation. We performed long duration (~12 h), high-density silicon probe recordings from rat hippocampal CA1 neurons, in animals that were either sleeping or sleep deprived following exposure to a novel maze environment. We found that SWRs showed a sustained rate of activity during sleep deprivation, similar to or higher than in natural sleep, but with decreased amplitudes for the sharp-waves combined with higher frequencies for the ripples. Furthermore, while hippocampal pyramidal cells showed a log-normal distribution of firing rates during sleep, these distributions were negatively skewed with a higher mean firing rate in both pyramidal cells and interneurons during sleep deprivation. During SWRs, however, firing rates were remarkably similar between both groups. Despite the abundant quantity of SWRs and the robust firing activity during these events in both groups, we found that reactivation of neurons was either completely abolished or significantly diminished during sleep deprivation compared to sleep. Interestingly, reactivation partially rebounded upon recovery sleep, but failed to reach the levels characteristic of natural sleep. Similarly, the number of replays were significantly lower during sleep deprivation and recovery sleep compared to natural sleep. These results provide a network-level account for the negative impact of sleep loss on hippocampal function and demonstrate that sleep loss impacts memory storage by causing a dissociation between the amount of SWRs and the replays and reactivations that take place during these events.
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spelling pubmed-99492502023-02-24 Sleep loss diminishes hippocampal reactivation and replay Giri, Bapun Kaya, Utku Maboudi, Kourosh Abel, Ted Diba, Kamran Res Sq Article Memories benefit from sleep, and sleep loss immediately following learning has a negative impact on subsequent memory storage. Several prominent hypotheses ascribe a central role to hippocampal sharp-wave ripples (SWRs), and the concurrent reactivation and replay of neuronal patterns from waking experience, in the offline memory consolidation process that occurs during sleep. However, little is known about how SWRs, reactivation, and replay are affected when animals are subjected to sleep deprivation. We performed long duration (~12 h), high-density silicon probe recordings from rat hippocampal CA1 neurons, in animals that were either sleeping or sleep deprived following exposure to a novel maze environment. We found that SWRs showed a sustained rate of activity during sleep deprivation, similar to or higher than in natural sleep, but with decreased amplitudes for the sharp-waves combined with higher frequencies for the ripples. Furthermore, while hippocampal pyramidal cells showed a log-normal distribution of firing rates during sleep, these distributions were negatively skewed with a higher mean firing rate in both pyramidal cells and interneurons during sleep deprivation. During SWRs, however, firing rates were remarkably similar between both groups. Despite the abundant quantity of SWRs and the robust firing activity during these events in both groups, we found that reactivation of neurons was either completely abolished or significantly diminished during sleep deprivation compared to sleep. Interestingly, reactivation partially rebounded upon recovery sleep, but failed to reach the levels characteristic of natural sleep. Similarly, the number of replays were significantly lower during sleep deprivation and recovery sleep compared to natural sleep. These results provide a network-level account for the negative impact of sleep loss on hippocampal function and demonstrate that sleep loss impacts memory storage by causing a dissociation between the amount of SWRs and the replays and reactivations that take place during these events. American Journal Experts 2023-02-16 /pmc/articles/PMC9949250/ /pubmed/36824950 http://dx.doi.org/10.21203/rs.3.rs-2540186/v1 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. https://creativecommons.org/licenses/by/4.0/License: This work is licensed under a Creative Commons Attribution 4.0 International License. Read Full License (https://creativecommons.org/licenses/by/4.0/)
spellingShingle Article
Giri, Bapun
Kaya, Utku
Maboudi, Kourosh
Abel, Ted
Diba, Kamran
Sleep loss diminishes hippocampal reactivation and replay
title Sleep loss diminishes hippocampal reactivation and replay
title_full Sleep loss diminishes hippocampal reactivation and replay
title_fullStr Sleep loss diminishes hippocampal reactivation and replay
title_full_unstemmed Sleep loss diminishes hippocampal reactivation and replay
title_short Sleep loss diminishes hippocampal reactivation and replay
title_sort sleep loss diminishes hippocampal reactivation and replay
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9949250/
https://www.ncbi.nlm.nih.gov/pubmed/36824950
http://dx.doi.org/10.21203/rs.3.rs-2540186/v1
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