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Altered sleep behavior in a genetic mouse model of impaired fear extinction

Sleep disturbances are a common complaint of anxiety patients and constitute a hallmark feature of post-traumatic stress disorder (PTSD). Emerging evidence suggests that poor sleep is not only a secondary symptom of anxiety- and trauma-related disorders but represents a risk factor in their developm...

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Autores principales: Fritz, Eva Maria, Kreuzer, Matthias, Altunkaya, Alp, Singewald, Nicolas, Fenzl, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8076259/
https://www.ncbi.nlm.nih.gov/pubmed/33903668
http://dx.doi.org/10.1038/s41598-021-88475-2
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author Fritz, Eva Maria
Kreuzer, Matthias
Altunkaya, Alp
Singewald, Nicolas
Fenzl, Thomas
author_facet Fritz, Eva Maria
Kreuzer, Matthias
Altunkaya, Alp
Singewald, Nicolas
Fenzl, Thomas
author_sort Fritz, Eva Maria
collection PubMed
description Sleep disturbances are a common complaint of anxiety patients and constitute a hallmark feature of post-traumatic stress disorder (PTSD). Emerging evidence suggests that poor sleep is not only a secondary symptom of anxiety- and trauma-related disorders but represents a risk factor in their development, for example by interfering with emotional memory processing. Fear extinction is a critical mechanism for the attenuation of fearful and traumatic memories and multiple studies suggest that healthy sleep is crucial for the formation of extinction memories. However, fear extinction is often impaired in anxiety- and trauma-related disorders—an endophenotype that is perfectly modelled in the 129S1/SvImJ inbred mouse strain. To investigate whether these mice exhibit altered sleep at baseline that could predispose them towards maladaptive fear processing, we compared their circadian sleep/wake patterns to those of typically extinction-competent C57BL/6 mice. We found significant differences regarding diurnal distribution of sleep and wakefulness, but also sleep architecture, spectral features and sleep spindle events. With regard to sleep disturbances reported by anxiety- and PTSD patients, our findings strengthen the 129S1/SvImJ mouse models’ face validity and highlight it as a platform to investigate novel, sleep-focused diagnostic and therapeutic strategies. Whether the identified alterations causally contribute to its pathological anxiety/PTSD-like phenotype will, however, have to be addressed in future studies.
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spelling pubmed-80762592021-04-27 Altered sleep behavior in a genetic mouse model of impaired fear extinction Fritz, Eva Maria Kreuzer, Matthias Altunkaya, Alp Singewald, Nicolas Fenzl, Thomas Sci Rep Article Sleep disturbances are a common complaint of anxiety patients and constitute a hallmark feature of post-traumatic stress disorder (PTSD). Emerging evidence suggests that poor sleep is not only a secondary symptom of anxiety- and trauma-related disorders but represents a risk factor in their development, for example by interfering with emotional memory processing. Fear extinction is a critical mechanism for the attenuation of fearful and traumatic memories and multiple studies suggest that healthy sleep is crucial for the formation of extinction memories. However, fear extinction is often impaired in anxiety- and trauma-related disorders—an endophenotype that is perfectly modelled in the 129S1/SvImJ inbred mouse strain. To investigate whether these mice exhibit altered sleep at baseline that could predispose them towards maladaptive fear processing, we compared their circadian sleep/wake patterns to those of typically extinction-competent C57BL/6 mice. We found significant differences regarding diurnal distribution of sleep and wakefulness, but also sleep architecture, spectral features and sleep spindle events. With regard to sleep disturbances reported by anxiety- and PTSD patients, our findings strengthen the 129S1/SvImJ mouse models’ face validity and highlight it as a platform to investigate novel, sleep-focused diagnostic and therapeutic strategies. Whether the identified alterations causally contribute to its pathological anxiety/PTSD-like phenotype will, however, have to be addressed in future studies. Nature Publishing Group UK 2021-04-26 /pmc/articles/PMC8076259/ /pubmed/33903668 http://dx.doi.org/10.1038/s41598-021-88475-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Fritz, Eva Maria
Kreuzer, Matthias
Altunkaya, Alp
Singewald, Nicolas
Fenzl, Thomas
Altered sleep behavior in a genetic mouse model of impaired fear extinction
title Altered sleep behavior in a genetic mouse model of impaired fear extinction
title_full Altered sleep behavior in a genetic mouse model of impaired fear extinction
title_fullStr Altered sleep behavior in a genetic mouse model of impaired fear extinction
title_full_unstemmed Altered sleep behavior in a genetic mouse model of impaired fear extinction
title_short Altered sleep behavior in a genetic mouse model of impaired fear extinction
title_sort altered sleep behavior in a genetic mouse model of impaired fear extinction
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8076259/
https://www.ncbi.nlm.nih.gov/pubmed/33903668
http://dx.doi.org/10.1038/s41598-021-88475-2
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