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A short pre-conception bout of predation risk affects both children and grandchildren
Traumatic events that affect physiology and behavior in the current generation may also impact future generations. We demonstrate that an ecologically realistic degree of predation risk prior to conception causes lasting changes in the first filial (F1) and second filial (F2) generations. We exposed...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10322924/ https://www.ncbi.nlm.nih.gov/pubmed/37407623 http://dx.doi.org/10.1038/s41598-023-37455-9 |
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author | Bhattacharya, Sriya MacCallum, Phillip E. Dayma, Mrunal McGrath-Janes, Andrea King, Brianna Dawson, Laura Bambico, Francis R. Berry, Mark D. Yuan, Qi Martin, Gerard M. Preisser, Evan L. Blundell, Jacqueline J. |
author_facet | Bhattacharya, Sriya MacCallum, Phillip E. Dayma, Mrunal McGrath-Janes, Andrea King, Brianna Dawson, Laura Bambico, Francis R. Berry, Mark D. Yuan, Qi Martin, Gerard M. Preisser, Evan L. Blundell, Jacqueline J. |
author_sort | Bhattacharya, Sriya |
collection | PubMed |
description | Traumatic events that affect physiology and behavior in the current generation may also impact future generations. We demonstrate that an ecologically realistic degree of predation risk prior to conception causes lasting changes in the first filial (F1) and second filial (F2) generations. We exposed male and female mice to a live rat (predator stress) or control (non-predator) condition for 5 min. Ten days later, stressed males and females were bred together as were control males and females. Adult F1 offspring from preconception-stressed parents responded to a mild stressor with more anxiety-like behavior and hyperarousal than offspring from control parents. Exposing these F1 offspring to the mild stressor increased neuronal activity (cFOS) in the hippocampus and altered glucocorticoid system function peripherally (plasma corticosterone levels). Even without the mild stressor, F1 offspring from preconception-stressed parents still exhibited more anxiety-like behaviors than controls. Cross-fostering studies confirmed that preconception stress, not maternal social environment, determined offspring behavioral phenotype. The effects of preconception parental stress were also unexpectedly persistent and produced similar behavioral phenotypes in the F2 offspring. Our data illustrate that a surprisingly small amount of preconception predator stress alters the brain, physiology, and behavior of future generations. A better understanding of the ‘long shadow’ cast by fearful events is critical for understanding the adaptive costs and benefits of transgenerational plasticity. It also suggests the intriguing possibility that similar risk-induced changes are the rule rather than the exception in free-living organisms, and that such multigenerational impacts are as ubiquitous as they are cryptic. |
format | Online Article Text |
id | pubmed-10322924 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-103229242023-07-07 A short pre-conception bout of predation risk affects both children and grandchildren Bhattacharya, Sriya MacCallum, Phillip E. Dayma, Mrunal McGrath-Janes, Andrea King, Brianna Dawson, Laura Bambico, Francis R. Berry, Mark D. Yuan, Qi Martin, Gerard M. Preisser, Evan L. Blundell, Jacqueline J. Sci Rep Article Traumatic events that affect physiology and behavior in the current generation may also impact future generations. We demonstrate that an ecologically realistic degree of predation risk prior to conception causes lasting changes in the first filial (F1) and second filial (F2) generations. We exposed male and female mice to a live rat (predator stress) or control (non-predator) condition for 5 min. Ten days later, stressed males and females were bred together as were control males and females. Adult F1 offspring from preconception-stressed parents responded to a mild stressor with more anxiety-like behavior and hyperarousal than offspring from control parents. Exposing these F1 offspring to the mild stressor increased neuronal activity (cFOS) in the hippocampus and altered glucocorticoid system function peripherally (plasma corticosterone levels). Even without the mild stressor, F1 offspring from preconception-stressed parents still exhibited more anxiety-like behaviors than controls. Cross-fostering studies confirmed that preconception stress, not maternal social environment, determined offspring behavioral phenotype. The effects of preconception parental stress were also unexpectedly persistent and produced similar behavioral phenotypes in the F2 offspring. Our data illustrate that a surprisingly small amount of preconception predator stress alters the brain, physiology, and behavior of future generations. A better understanding of the ‘long shadow’ cast by fearful events is critical for understanding the adaptive costs and benefits of transgenerational plasticity. It also suggests the intriguing possibility that similar risk-induced changes are the rule rather than the exception in free-living organisms, and that such multigenerational impacts are as ubiquitous as they are cryptic. Nature Publishing Group UK 2023-07-05 /pmc/articles/PMC10322924/ /pubmed/37407623 http://dx.doi.org/10.1038/s41598-023-37455-9 Text en © The Author(s) 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 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 Bhattacharya, Sriya MacCallum, Phillip E. Dayma, Mrunal McGrath-Janes, Andrea King, Brianna Dawson, Laura Bambico, Francis R. Berry, Mark D. Yuan, Qi Martin, Gerard M. Preisser, Evan L. Blundell, Jacqueline J. A short pre-conception bout of predation risk affects both children and grandchildren |
title | A short pre-conception bout of predation risk affects both children and grandchildren |
title_full | A short pre-conception bout of predation risk affects both children and grandchildren |
title_fullStr | A short pre-conception bout of predation risk affects both children and grandchildren |
title_full_unstemmed | A short pre-conception bout of predation risk affects both children and grandchildren |
title_short | A short pre-conception bout of predation risk affects both children and grandchildren |
title_sort | short pre-conception bout of predation risk affects both children and grandchildren |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10322924/ https://www.ncbi.nlm.nih.gov/pubmed/37407623 http://dx.doi.org/10.1038/s41598-023-37455-9 |
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