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

Abstract 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...

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Autores principales: Eva Maria Fritz, Matthias Kreuzer, Alp Altunkaya, Nicolas Singewald, Thomas Fenzl
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Lenguaje:EN
Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/761b8f8d93844bb1bd67bb3a367b3968
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spelling oai:doaj.org-article:761b8f8d93844bb1bd67bb3a367b39682021-12-02T13:41:43ZAltered sleep behavior in a genetic mouse model of impaired fear extinction10.1038/s41598-021-88475-22045-2322https://doaj.org/article/761b8f8d93844bb1bd67bb3a367b39682021-04-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-88475-2https://doaj.org/toc/2045-2322Abstract 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.Eva Maria FritzMatthias KreuzerAlp AltunkayaNicolas SingewaldThomas FenzlNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-16 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Eva Maria Fritz
Matthias Kreuzer
Alp Altunkaya
Nicolas Singewald
Thomas Fenzl
Altered sleep behavior in a genetic mouse model of impaired fear extinction
description Abstract 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.
format article
author Eva Maria Fritz
Matthias Kreuzer
Alp Altunkaya
Nicolas Singewald
Thomas Fenzl
author_facet Eva Maria Fritz
Matthias Kreuzer
Alp Altunkaya
Nicolas Singewald
Thomas Fenzl
author_sort Eva Maria Fritz
title 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_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_sort altered sleep behavior in a genetic mouse model of impaired fear extinction
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/761b8f8d93844bb1bd67bb3a367b3968
work_keys_str_mv AT evamariafritz alteredsleepbehaviorinageneticmousemodelofimpairedfearextinction
AT matthiaskreuzer alteredsleepbehaviorinageneticmousemodelofimpairedfearextinction
AT alpaltunkaya alteredsleepbehaviorinageneticmousemodelofimpairedfearextinction
AT nicolassingewald alteredsleepbehaviorinageneticmousemodelofimpairedfearextinction
AT thomasfenzl alteredsleepbehaviorinageneticmousemodelofimpairedfearextinction
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