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Combined space stressors induce independent behavioral deficits predicted by early peripheral blood monocytes
Interplanetary space travel poses many hazards to the human body. To protect astronaut health and performance on critical missions, there is first a need to understand the effects of deep space hazards, including ionizing radiation, confinement, and altered gravity. Previous studies of rodents expos...
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/PMC9889764/ https://www.ncbi.nlm.nih.gov/pubmed/36720960 http://dx.doi.org/10.1038/s41598-023-28508-0 |
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author | Rienecker, Kira D. A. Grue, Katherine Paladini, Maria Serena Frias, Elma S. Frattini, Valentina Borlongan, Mia C. Chou, Austin Torres-Espin, Abel Krukowski, Karen Ferguson, Adam R. Rosi, Susanna |
author_facet | Rienecker, Kira D. A. Grue, Katherine Paladini, Maria Serena Frias, Elma S. Frattini, Valentina Borlongan, Mia C. Chou, Austin Torres-Espin, Abel Krukowski, Karen Ferguson, Adam R. Rosi, Susanna |
author_sort | Rienecker, Kira D. A. |
collection | PubMed |
description | Interplanetary space travel poses many hazards to the human body. To protect astronaut health and performance on critical missions, there is first a need to understand the effects of deep space hazards, including ionizing radiation, confinement, and altered gravity. Previous studies of rodents exposed to a single such stressor document significant deficits, but our study is the first to investigate possible cumulative and synergistic impacts of simultaneous ionizing radiation, confinement, and altered gravity on behavior and cognition. Our cohort was divided between 6-month-old female and male mice in group, social isolation, or hindlimb unloading housing, exposed to 0 or 50 cGy of 5 ion simplified simulated galactic cosmic radiation (GCRsim). We report interactions and independent effects of GCRsim exposure and housing conditions on behavioral and cognitive performance. Exposure to GCRsim drove changes in immune cell populations in peripheral blood collected early after irradiation, while housing conditions drove changes in blood collected at a later point. Female mice were largely resilient to deficits observed in male mice. Finally, we used principal component analysis to represent total deficits as principal component scores, which were predicted by general linear models using GCR exposure, housing condition, and early blood biomarkers. |
format | Online Article Text |
id | pubmed-9889764 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98897642023-02-02 Combined space stressors induce independent behavioral deficits predicted by early peripheral blood monocytes Rienecker, Kira D. A. Grue, Katherine Paladini, Maria Serena Frias, Elma S. Frattini, Valentina Borlongan, Mia C. Chou, Austin Torres-Espin, Abel Krukowski, Karen Ferguson, Adam R. Rosi, Susanna Sci Rep Article Interplanetary space travel poses many hazards to the human body. To protect astronaut health and performance on critical missions, there is first a need to understand the effects of deep space hazards, including ionizing radiation, confinement, and altered gravity. Previous studies of rodents exposed to a single such stressor document significant deficits, but our study is the first to investigate possible cumulative and synergistic impacts of simultaneous ionizing radiation, confinement, and altered gravity on behavior and cognition. Our cohort was divided between 6-month-old female and male mice in group, social isolation, or hindlimb unloading housing, exposed to 0 or 50 cGy of 5 ion simplified simulated galactic cosmic radiation (GCRsim). We report interactions and independent effects of GCRsim exposure and housing conditions on behavioral and cognitive performance. Exposure to GCRsim drove changes in immune cell populations in peripheral blood collected early after irradiation, while housing conditions drove changes in blood collected at a later point. Female mice were largely resilient to deficits observed in male mice. Finally, we used principal component analysis to represent total deficits as principal component scores, which were predicted by general linear models using GCR exposure, housing condition, and early blood biomarkers. Nature Publishing Group UK 2023-01-31 /pmc/articles/PMC9889764/ /pubmed/36720960 http://dx.doi.org/10.1038/s41598-023-28508-0 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 Rienecker, Kira D. A. Grue, Katherine Paladini, Maria Serena Frias, Elma S. Frattini, Valentina Borlongan, Mia C. Chou, Austin Torres-Espin, Abel Krukowski, Karen Ferguson, Adam R. Rosi, Susanna Combined space stressors induce independent behavioral deficits predicted by early peripheral blood monocytes |
title | Combined space stressors induce independent behavioral deficits predicted by early peripheral blood monocytes |
title_full | Combined space stressors induce independent behavioral deficits predicted by early peripheral blood monocytes |
title_fullStr | Combined space stressors induce independent behavioral deficits predicted by early peripheral blood monocytes |
title_full_unstemmed | Combined space stressors induce independent behavioral deficits predicted by early peripheral blood monocytes |
title_short | Combined space stressors induce independent behavioral deficits predicted by early peripheral blood monocytes |
title_sort | combined space stressors induce independent behavioral deficits predicted by early peripheral blood monocytes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9889764/ https://www.ncbi.nlm.nih.gov/pubmed/36720960 http://dx.doi.org/10.1038/s41598-023-28508-0 |
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