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Epigenetic determinants of space radiation-induced cognitive dysfunction

Among the dangers to astronauts engaging in deep space missions such as a Mars expedition is exposure to radiations that put them at risk for severe cognitive dysfunction. These radiation-induced cognitive impairments are accompanied by functional and structural changes including oxidative stress, n...

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Autores principales: Acharya, Munjal M., Baddour, Al Anoud D., Kawashita, Takumi, Allen, Barrett D., Syage, Amber R., Nguyen, Thuan H., Yoon, Nicole, Giedzinski, Erich, Yu, Liping, Parihar, Vipan K., Baulch, Janet E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5318883/
https://www.ncbi.nlm.nih.gov/pubmed/28220892
http://dx.doi.org/10.1038/srep42885
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author Acharya, Munjal M.
Baddour, Al Anoud D.
Kawashita, Takumi
Allen, Barrett D.
Syage, Amber R.
Nguyen, Thuan H.
Yoon, Nicole
Giedzinski, Erich
Yu, Liping
Parihar, Vipan K.
Baulch, Janet E.
author_facet Acharya, Munjal M.
Baddour, Al Anoud D.
Kawashita, Takumi
Allen, Barrett D.
Syage, Amber R.
Nguyen, Thuan H.
Yoon, Nicole
Giedzinski, Erich
Yu, Liping
Parihar, Vipan K.
Baulch, Janet E.
author_sort Acharya, Munjal M.
collection PubMed
description Among the dangers to astronauts engaging in deep space missions such as a Mars expedition is exposure to radiations that put them at risk for severe cognitive dysfunction. These radiation-induced cognitive impairments are accompanied by functional and structural changes including oxidative stress, neuroinflammation, and degradation of neuronal architecture. The molecular mechanisms that dictate CNS function are multifaceted and it is unclear how irradiation induces persistent alterations in the brain. Among those determinants of cognitive function are neuroepigenetic mechanisms that translate radiation responses into altered gene expression and cellular phenotype. In this study, we have demonstrated a correlation between epigenetic aberrations and adverse effects of space relevant irradiation on cognition. In cognitively impaired irradiated mice we observed increased 5-methylcytosine and 5-hydroxymethylcytosine levels in the hippocampus that coincided with increased levels of the DNA methylating enzymes DNMT3a, TET1 and TET3. By inhibiting methylation using 5-iodotubercidin, we demonstrated amelioration of the epigenetic effects of irradiation. In addition to protecting against those molecular effects of irradiation, 5-iodotubercidin restored behavioral performance to that of unirradiated animals. The findings of this study establish the possibility that neuroepigenetic mechanisms significantly contribute to the functional and structural changes that affect the irradiated brain and cognition.
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spelling pubmed-53188832017-02-24 Epigenetic determinants of space radiation-induced cognitive dysfunction Acharya, Munjal M. Baddour, Al Anoud D. Kawashita, Takumi Allen, Barrett D. Syage, Amber R. Nguyen, Thuan H. Yoon, Nicole Giedzinski, Erich Yu, Liping Parihar, Vipan K. Baulch, Janet E. Sci Rep Article Among the dangers to astronauts engaging in deep space missions such as a Mars expedition is exposure to radiations that put them at risk for severe cognitive dysfunction. These radiation-induced cognitive impairments are accompanied by functional and structural changes including oxidative stress, neuroinflammation, and degradation of neuronal architecture. The molecular mechanisms that dictate CNS function are multifaceted and it is unclear how irradiation induces persistent alterations in the brain. Among those determinants of cognitive function are neuroepigenetic mechanisms that translate radiation responses into altered gene expression and cellular phenotype. In this study, we have demonstrated a correlation between epigenetic aberrations and adverse effects of space relevant irradiation on cognition. In cognitively impaired irradiated mice we observed increased 5-methylcytosine and 5-hydroxymethylcytosine levels in the hippocampus that coincided with increased levels of the DNA methylating enzymes DNMT3a, TET1 and TET3. By inhibiting methylation using 5-iodotubercidin, we demonstrated amelioration of the epigenetic effects of irradiation. In addition to protecting against those molecular effects of irradiation, 5-iodotubercidin restored behavioral performance to that of unirradiated animals. The findings of this study establish the possibility that neuroepigenetic mechanisms significantly contribute to the functional and structural changes that affect the irradiated brain and cognition. Nature Publishing Group 2017-02-21 /pmc/articles/PMC5318883/ /pubmed/28220892 http://dx.doi.org/10.1038/srep42885 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Acharya, Munjal M.
Baddour, Al Anoud D.
Kawashita, Takumi
Allen, Barrett D.
Syage, Amber R.
Nguyen, Thuan H.
Yoon, Nicole
Giedzinski, Erich
Yu, Liping
Parihar, Vipan K.
Baulch, Janet E.
Epigenetic determinants of space radiation-induced cognitive dysfunction
title Epigenetic determinants of space radiation-induced cognitive dysfunction
title_full Epigenetic determinants of space radiation-induced cognitive dysfunction
title_fullStr Epigenetic determinants of space radiation-induced cognitive dysfunction
title_full_unstemmed Epigenetic determinants of space radiation-induced cognitive dysfunction
title_short Epigenetic determinants of space radiation-induced cognitive dysfunction
title_sort epigenetic determinants of space radiation-induced cognitive dysfunction
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5318883/
https://www.ncbi.nlm.nih.gov/pubmed/28220892
http://dx.doi.org/10.1038/srep42885
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