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Restraint stress of female mice during oocyte development facilitates oocyte postovulatory aging

Studies suggest that psychological stress on women can impair their reproduction and that postovulatory oocyte aging (POA) might increase the risk of early pregnancy loss and affect offspring’s reproductive fitness and longevity. However, whether psychological stress during oocyte development would...

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Autores principales: Chen, Ren-Ren, Wang, Jia, Zhang, Min, Kong, Qiao-Qiao, Sun, Guang-Yi, Jin, Chun-Hui, Luo, Ming-Jiu, Tan, Jing-He
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9740362/
https://www.ncbi.nlm.nih.gov/pubmed/36441534
http://dx.doi.org/10.18632/aging.204400
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author Chen, Ren-Ren
Wang, Jia
Zhang, Min
Kong, Qiao-Qiao
Sun, Guang-Yi
Jin, Chun-Hui
Luo, Ming-Jiu
Tan, Jing-He
author_facet Chen, Ren-Ren
Wang, Jia
Zhang, Min
Kong, Qiao-Qiao
Sun, Guang-Yi
Jin, Chun-Hui
Luo, Ming-Jiu
Tan, Jing-He
author_sort Chen, Ren-Ren
collection PubMed
description Studies suggest that psychological stress on women can impair their reproduction and that postovulatory oocyte aging (POA) might increase the risk of early pregnancy loss and affect offspring’s reproductive fitness and longevity. However, whether psychological stress during oocyte development would facilitate POA is unknown but worth exploring to understand the mechanisms by which psychological stress and POA damage oocytes. This study observed effects of female restraint stress during oocyte development (FRSOD) on oocyte resistance to POA. Female mice were restrained for 48 h before superovulation, and they were sacrificed at different intervals after ovulation to recover aging oocytes for analyzing their early and late aged characteristics. The effects of FRSOD on aging oocytes included: (1) increasing their susceptibility to activation stimulus with elevated cytoplasmic calcium; (2) impairing their developmental potential with downregulated expression of development-beneficial genes; (3) facilitating degeneration, cytoplasmic fragmentation and apoptosis; (4) worsening the disorganization of cortical granules and spindle/chromosomes; and (5) impairing redox potential with increased oxidative stress. In conclusion, FRSOD impairs oocyte resistance to POA, so that stressed oocytes become aged significantly quicker than unstressed controls. Thus, couples wishing to achieve pregnancy should take steps to avoid not only fertilization of aged oocytes but also pregestational stressful life events.
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spelling pubmed-97403622022-12-12 Restraint stress of female mice during oocyte development facilitates oocyte postovulatory aging Chen, Ren-Ren Wang, Jia Zhang, Min Kong, Qiao-Qiao Sun, Guang-Yi Jin, Chun-Hui Luo, Ming-Jiu Tan, Jing-He Aging (Albany NY) Research Paper Studies suggest that psychological stress on women can impair their reproduction and that postovulatory oocyte aging (POA) might increase the risk of early pregnancy loss and affect offspring’s reproductive fitness and longevity. However, whether psychological stress during oocyte development would facilitate POA is unknown but worth exploring to understand the mechanisms by which psychological stress and POA damage oocytes. This study observed effects of female restraint stress during oocyte development (FRSOD) on oocyte resistance to POA. Female mice were restrained for 48 h before superovulation, and they were sacrificed at different intervals after ovulation to recover aging oocytes for analyzing their early and late aged characteristics. The effects of FRSOD on aging oocytes included: (1) increasing their susceptibility to activation stimulus with elevated cytoplasmic calcium; (2) impairing their developmental potential with downregulated expression of development-beneficial genes; (3) facilitating degeneration, cytoplasmic fragmentation and apoptosis; (4) worsening the disorganization of cortical granules and spindle/chromosomes; and (5) impairing redox potential with increased oxidative stress. In conclusion, FRSOD impairs oocyte resistance to POA, so that stressed oocytes become aged significantly quicker than unstressed controls. Thus, couples wishing to achieve pregnancy should take steps to avoid not only fertilization of aged oocytes but also pregestational stressful life events. Impact Journals 2022-11-26 /pmc/articles/PMC9740362/ /pubmed/36441534 http://dx.doi.org/10.18632/aging.204400 Text en Copyright: © 2022 Chen et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Chen, Ren-Ren
Wang, Jia
Zhang, Min
Kong, Qiao-Qiao
Sun, Guang-Yi
Jin, Chun-Hui
Luo, Ming-Jiu
Tan, Jing-He
Restraint stress of female mice during oocyte development facilitates oocyte postovulatory aging
title Restraint stress of female mice during oocyte development facilitates oocyte postovulatory aging
title_full Restraint stress of female mice during oocyte development facilitates oocyte postovulatory aging
title_fullStr Restraint stress of female mice during oocyte development facilitates oocyte postovulatory aging
title_full_unstemmed Restraint stress of female mice during oocyte development facilitates oocyte postovulatory aging
title_short Restraint stress of female mice during oocyte development facilitates oocyte postovulatory aging
title_sort restraint stress of female mice during oocyte development facilitates oocyte postovulatory aging
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9740362/
https://www.ncbi.nlm.nih.gov/pubmed/36441534
http://dx.doi.org/10.18632/aging.204400
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