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Life-long brain compensatory responses to galactic cosmic radiation exposure
Galactic cosmic radiation (GCR) composed of high-energy, heavy particles (HZE) poses potentially serious hazards to long-duration crewed missions in deep space beyond earth’s magnetosphere, including planned missions to Mars. Chronic effects of GCR exposure on brain structure and cognitive function...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7900210/ https://www.ncbi.nlm.nih.gov/pubmed/33619310 http://dx.doi.org/10.1038/s41598-021-83447-y |
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author | Miry, Omid Zhang, Xiao-lei Vose, Linnea R. Gopaul, Katisha R. Subah, Galadu Moncaster, Juliet A. Wojnarowicz, Mark W. Fisher, Andrew M. Tagge, Chad A. Goldstein, Lee E. Stanton, Patric K. |
author_facet | Miry, Omid Zhang, Xiao-lei Vose, Linnea R. Gopaul, Katisha R. Subah, Galadu Moncaster, Juliet A. Wojnarowicz, Mark W. Fisher, Andrew M. Tagge, Chad A. Goldstein, Lee E. Stanton, Patric K. |
author_sort | Miry, Omid |
collection | PubMed |
description | Galactic cosmic radiation (GCR) composed of high-energy, heavy particles (HZE) poses potentially serious hazards to long-duration crewed missions in deep space beyond earth’s magnetosphere, including planned missions to Mars. Chronic effects of GCR exposure on brain structure and cognitive function are poorly understood, thereby limiting risk reduction and mitigation strategies to protect against sequelae from exposure during and after deep-space travel. Given the selective vulnerability of the hippocampus to neurotoxic insult and the importance of this brain region to learning and memory, we hypothesized that GCR-relevant HZE exposure may induce long-term alterations in adult hippocampal neurogenesis, synaptic plasticity, and hippocampal-dependent learning and memory. To test this hypothesis, we irradiated 3-month-old male and female mice with a single, whole-body dose of 10, 50, or 100 cGy (56)Fe ions (600 MeV, 181 keV/μm) at Brookhaven National Laboratory. Our data reveal complex, dynamic, time-dependent effects of HZE exposure on the hippocampus. Two months post exposure, neurogenesis, synaptic plasticity and learning were impaired compared to sham-irradiated, age-matched controls. By six months post-exposure, deficits in spatial learning were absent in irradiated mice, and synaptic potentiation was enhanced. Enhanced performance in spatial learning and facilitation of synaptic plasticity in irradiated mice persisted 12 months post-exposure, concomitant with a dramatic rebound in adult-born neurons. Synaptic plasticity and spatial learning remained enhanced 20 months post-exposure, indicating a life-long influence on plasticity and cognition from a single exposure to HZE in young adulthood. These findings suggest that GCR-exposure can persistently alter brain health and cognitive function during and after long-duration travel in deep space. |
format | Online Article Text |
id | pubmed-7900210 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79002102021-02-24 Life-long brain compensatory responses to galactic cosmic radiation exposure Miry, Omid Zhang, Xiao-lei Vose, Linnea R. Gopaul, Katisha R. Subah, Galadu Moncaster, Juliet A. Wojnarowicz, Mark W. Fisher, Andrew M. Tagge, Chad A. Goldstein, Lee E. Stanton, Patric K. Sci Rep Article Galactic cosmic radiation (GCR) composed of high-energy, heavy particles (HZE) poses potentially serious hazards to long-duration crewed missions in deep space beyond earth’s magnetosphere, including planned missions to Mars. Chronic effects of GCR exposure on brain structure and cognitive function are poorly understood, thereby limiting risk reduction and mitigation strategies to protect against sequelae from exposure during and after deep-space travel. Given the selective vulnerability of the hippocampus to neurotoxic insult and the importance of this brain region to learning and memory, we hypothesized that GCR-relevant HZE exposure may induce long-term alterations in adult hippocampal neurogenesis, synaptic plasticity, and hippocampal-dependent learning and memory. To test this hypothesis, we irradiated 3-month-old male and female mice with a single, whole-body dose of 10, 50, or 100 cGy (56)Fe ions (600 MeV, 181 keV/μm) at Brookhaven National Laboratory. Our data reveal complex, dynamic, time-dependent effects of HZE exposure on the hippocampus. Two months post exposure, neurogenesis, synaptic plasticity and learning were impaired compared to sham-irradiated, age-matched controls. By six months post-exposure, deficits in spatial learning were absent in irradiated mice, and synaptic potentiation was enhanced. Enhanced performance in spatial learning and facilitation of synaptic plasticity in irradiated mice persisted 12 months post-exposure, concomitant with a dramatic rebound in adult-born neurons. Synaptic plasticity and spatial learning remained enhanced 20 months post-exposure, indicating a life-long influence on plasticity and cognition from a single exposure to HZE in young adulthood. These findings suggest that GCR-exposure can persistently alter brain health and cognitive function during and after long-duration travel in deep space. Nature Publishing Group UK 2021-02-22 /pmc/articles/PMC7900210/ /pubmed/33619310 http://dx.doi.org/10.1038/s41598-021-83447-y Text en © The Author(s) 2021 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/. |
spellingShingle | Article Miry, Omid Zhang, Xiao-lei Vose, Linnea R. Gopaul, Katisha R. Subah, Galadu Moncaster, Juliet A. Wojnarowicz, Mark W. Fisher, Andrew M. Tagge, Chad A. Goldstein, Lee E. Stanton, Patric K. Life-long brain compensatory responses to galactic cosmic radiation exposure |
title | Life-long brain compensatory responses to galactic cosmic radiation exposure |
title_full | Life-long brain compensatory responses to galactic cosmic radiation exposure |
title_fullStr | Life-long brain compensatory responses to galactic cosmic radiation exposure |
title_full_unstemmed | Life-long brain compensatory responses to galactic cosmic radiation exposure |
title_short | Life-long brain compensatory responses to galactic cosmic radiation exposure |
title_sort | life-long brain compensatory responses to galactic cosmic radiation exposure |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7900210/ https://www.ncbi.nlm.nih.gov/pubmed/33619310 http://dx.doi.org/10.1038/s41598-021-83447-y |
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