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The estrous cycle modulates early-life adversity effects on mouse avoidance behavior through progesterone signaling
Early-life adversity (ELA) increases the likelihood of neuropsychiatric diagnoses, which are more prevalent in women than men. Since changes in reproductive hormone levels can also increase the probability of anxiety disorders in women, we examined the effects of ELA on adult female mice across the...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9729614/ https://www.ncbi.nlm.nih.gov/pubmed/36476469 http://dx.doi.org/10.1038/s41467-022-35068-w |
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author | Laham, Blake J. Murthy, Sahana S. Hanani, Monica Clappier, Mona Boyer, Sydney Vasquez, Betsy Gould, Elizabeth |
author_facet | Laham, Blake J. Murthy, Sahana S. Hanani, Monica Clappier, Mona Boyer, Sydney Vasquez, Betsy Gould, Elizabeth |
author_sort | Laham, Blake J. |
collection | PubMed |
description | Early-life adversity (ELA) increases the likelihood of neuropsychiatric diagnoses, which are more prevalent in women than men. Since changes in reproductive hormone levels can also increase the probability of anxiety disorders in women, we examined the effects of ELA on adult female mice across the estrous cycle. We found that during diestrus, when progesterone levels are relatively high, ELA mice exhibit increased avoidance behavior and increased theta oscillation power in the ventral hippocampus (vHIP). We also found that diestrus ELA mice had higher levels of progesterone and lower levels of allopregnanolone, a neurosteroid metabolite of progesterone, in the vHIP compared with control-reared mice. Progesterone receptor antagonism normalized avoidance behavior in ELA mice, while treatment with a negative allosteric modulator of allopregnanolone promoted avoidance behavior in control mice. These results suggest that altered vHIP progesterone and allopregnanolone signaling during diestrus increases avoidance behavior in ELA mice. |
format | Online Article Text |
id | pubmed-9729614 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-97296142022-12-09 The estrous cycle modulates early-life adversity effects on mouse avoidance behavior through progesterone signaling Laham, Blake J. Murthy, Sahana S. Hanani, Monica Clappier, Mona Boyer, Sydney Vasquez, Betsy Gould, Elizabeth Nat Commun Article Early-life adversity (ELA) increases the likelihood of neuropsychiatric diagnoses, which are more prevalent in women than men. Since changes in reproductive hormone levels can also increase the probability of anxiety disorders in women, we examined the effects of ELA on adult female mice across the estrous cycle. We found that during diestrus, when progesterone levels are relatively high, ELA mice exhibit increased avoidance behavior and increased theta oscillation power in the ventral hippocampus (vHIP). We also found that diestrus ELA mice had higher levels of progesterone and lower levels of allopregnanolone, a neurosteroid metabolite of progesterone, in the vHIP compared with control-reared mice. Progesterone receptor antagonism normalized avoidance behavior in ELA mice, while treatment with a negative allosteric modulator of allopregnanolone promoted avoidance behavior in control mice. These results suggest that altered vHIP progesterone and allopregnanolone signaling during diestrus increases avoidance behavior in ELA mice. Nature Publishing Group UK 2022-12-07 /pmc/articles/PMC9729614/ /pubmed/36476469 http://dx.doi.org/10.1038/s41467-022-35068-w Text en © The Author(s) 2022, corrected publication 2023 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Laham, Blake J. Murthy, Sahana S. Hanani, Monica Clappier, Mona Boyer, Sydney Vasquez, Betsy Gould, Elizabeth The estrous cycle modulates early-life adversity effects on mouse avoidance behavior through progesterone signaling |
title | The estrous cycle modulates early-life adversity effects on mouse avoidance behavior through progesterone signaling |
title_full | The estrous cycle modulates early-life adversity effects on mouse avoidance behavior through progesterone signaling |
title_fullStr | The estrous cycle modulates early-life adversity effects on mouse avoidance behavior through progesterone signaling |
title_full_unstemmed | The estrous cycle modulates early-life adversity effects on mouse avoidance behavior through progesterone signaling |
title_short | The estrous cycle modulates early-life adversity effects on mouse avoidance behavior through progesterone signaling |
title_sort | estrous cycle modulates early-life adversity effects on mouse avoidance behavior through progesterone signaling |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9729614/ https://www.ncbi.nlm.nih.gov/pubmed/36476469 http://dx.doi.org/10.1038/s41467-022-35068-w |
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