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Altered brain rhythms and behaviour in the accelerated ovarian failure mouse model of human menopause
To date, potential mechanisms of menopause-related memory and cognitive deficits have not been elucidated. Therefore, we studied brain oscillations, their phase–amplitude coupling, sleep and vigilance state patterns, running wheel use and other behavioural measures in a translationally valid mouse m...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9253886/ https://www.ncbi.nlm.nih.gov/pubmed/35794872 http://dx.doi.org/10.1093/braincomms/fcac166 |
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author | Vrontou, Sophia Bédécarrats, Alexis Wei, Xiaofei Ayodeji, Morikeoluwa Brassai, Attila Molnár, László Mody, Istvan |
author_facet | Vrontou, Sophia Bédécarrats, Alexis Wei, Xiaofei Ayodeji, Morikeoluwa Brassai, Attila Molnár, László Mody, Istvan |
author_sort | Vrontou, Sophia |
collection | PubMed |
description | To date, potential mechanisms of menopause-related memory and cognitive deficits have not been elucidated. Therefore, we studied brain oscillations, their phase–amplitude coupling, sleep and vigilance state patterns, running wheel use and other behavioural measures in a translationally valid mouse model of menopause, the 4-vinylcyclohexene-diepoxide-induced accelerated ovarian failure. After accelerated ovarian failure, female mice show significant alterations in brain rhythms, including changes in the frequencies of θ (5–12 Hz) and γ (30–120 Hz) oscillations, a reversed phase–amplitude coupling, altered coupling of hippocampal sharp-wave ripples to medial prefrontal cortical sleep spindles and reduced δ oscillation (0.5–4 Hz) synchrony between the two regions during non-rapid eye movement sleep. In addition, we report on significant circadian variations in the frequencies of θ and γ oscillations, and massive synchronous δ oscillations during wheel running. Our results reveal novel and specific network alterations and feasible signs for diminished brain connectivity in the accelerated ovarian failure mouse model of menopause. Taken together, our results may have identified changes possibly responsible for some of the memory and cognitive deficits previously described in this model. Corresponding future studies in menopausal women could shed light on fundamental mechanisms underlying the neurological and psychiatric comorbidities present during this important transitional phase in women’s lives. |
format | Online Article Text |
id | pubmed-9253886 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-92538862022-07-05 Altered brain rhythms and behaviour in the accelerated ovarian failure mouse model of human menopause Vrontou, Sophia Bédécarrats, Alexis Wei, Xiaofei Ayodeji, Morikeoluwa Brassai, Attila Molnár, László Mody, Istvan Brain Commun Original Article To date, potential mechanisms of menopause-related memory and cognitive deficits have not been elucidated. Therefore, we studied brain oscillations, their phase–amplitude coupling, sleep and vigilance state patterns, running wheel use and other behavioural measures in a translationally valid mouse model of menopause, the 4-vinylcyclohexene-diepoxide-induced accelerated ovarian failure. After accelerated ovarian failure, female mice show significant alterations in brain rhythms, including changes in the frequencies of θ (5–12 Hz) and γ (30–120 Hz) oscillations, a reversed phase–amplitude coupling, altered coupling of hippocampal sharp-wave ripples to medial prefrontal cortical sleep spindles and reduced δ oscillation (0.5–4 Hz) synchrony between the two regions during non-rapid eye movement sleep. In addition, we report on significant circadian variations in the frequencies of θ and γ oscillations, and massive synchronous δ oscillations during wheel running. Our results reveal novel and specific network alterations and feasible signs for diminished brain connectivity in the accelerated ovarian failure mouse model of menopause. Taken together, our results may have identified changes possibly responsible for some of the memory and cognitive deficits previously described in this model. Corresponding future studies in menopausal women could shed light on fundamental mechanisms underlying the neurological and psychiatric comorbidities present during this important transitional phase in women’s lives. Oxford University Press 2022-06-22 /pmc/articles/PMC9253886/ /pubmed/35794872 http://dx.doi.org/10.1093/braincomms/fcac166 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the Guarantors of Brain. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Vrontou, Sophia Bédécarrats, Alexis Wei, Xiaofei Ayodeji, Morikeoluwa Brassai, Attila Molnár, László Mody, Istvan Altered brain rhythms and behaviour in the accelerated ovarian failure mouse model of human menopause |
title | Altered brain rhythms and behaviour in the accelerated ovarian failure mouse model of human menopause |
title_full | Altered brain rhythms and behaviour in the accelerated ovarian failure mouse model of human menopause |
title_fullStr | Altered brain rhythms and behaviour in the accelerated ovarian failure mouse model of human menopause |
title_full_unstemmed | Altered brain rhythms and behaviour in the accelerated ovarian failure mouse model of human menopause |
title_short | Altered brain rhythms and behaviour in the accelerated ovarian failure mouse model of human menopause |
title_sort | altered brain rhythms and behaviour in the accelerated ovarian failure mouse model of human menopause |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9253886/ https://www.ncbi.nlm.nih.gov/pubmed/35794872 http://dx.doi.org/10.1093/braincomms/fcac166 |
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