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Galactic cosmic radiation exposure causes multifaceted neurocognitive impairments
Technological advancements have facilitated the implementation of realistic, terrestrial-based complex 33-beam galactic cosmic radiation simulations (GCR Sim) to now probe central nervous system functionality. This work expands considerably on prior, simplified GCR simulations, yielding new insights...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9823026/ https://www.ncbi.nlm.nih.gov/pubmed/36607431 http://dx.doi.org/10.1007/s00018-022-04666-8 |
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author | Alaghband, Yasaman Klein, Peter M. Kramár, Eniko A. Cranston, Michael N. Perry, Bayley C. Shelerud, Lukas M. Kane, Alice E. Doan, Ngoc-Lien Ru, Ning Acharya, Munjal M. Wood, Marcelo A. Sinclair, David A. Dickstein, Dara L. Soltesz, Ivan Limoli, Charles L. Baulch, Janet E. |
author_facet | Alaghband, Yasaman Klein, Peter M. Kramár, Eniko A. Cranston, Michael N. Perry, Bayley C. Shelerud, Lukas M. Kane, Alice E. Doan, Ngoc-Lien Ru, Ning Acharya, Munjal M. Wood, Marcelo A. Sinclair, David A. Dickstein, Dara L. Soltesz, Ivan Limoli, Charles L. Baulch, Janet E. |
author_sort | Alaghband, Yasaman |
collection | PubMed |
description | Technological advancements have facilitated the implementation of realistic, terrestrial-based complex 33-beam galactic cosmic radiation simulations (GCR Sim) to now probe central nervous system functionality. This work expands considerably on prior, simplified GCR simulations, yielding new insights into responses of male and female mice exposed to 40–50 cGy acute or chronic radiations relevant to deep space travel. Results of the object in updated location task suggested that exposure to acute or chronic GCR Sim induced persistent impairments in hippocampus-dependent memory formation and reconsolidation in female mice that did not manifest robustly in irradiated male mice. Interestingly, irradiated male mice, but not females, were impaired in novel object recognition and chronically irradiated males exhibited increased aggressive behavior on the tube dominance test. Electrophysiology studies used to evaluate synaptic plasticity in the hippocampal CA1 region revealed significant reductions in long-term potentiation after each irradiation paradigm in both sexes. Interestingly, network-level disruptions did not translate to altered intrinsic electrophysiological properties of CA1 pyramidal cells, whereas acute exposures caused modest drops in excitatory synaptic signaling in males. Ultrastructural analyses of CA1 synapses found smaller postsynaptic densities in larger spines of chronically exposed mice compared to controls and acutely exposed mice. Myelination was also affected by GCR Sim with acutely exposed mice exhibiting an increase in the percent of myelinated axons; however, the myelin sheathes on small calibur (< 0.3 mm) and larger (> 0.5 mm) axons were thinner when compared to controls. Present findings might have been predicted based on previous studies using single and mixed beam exposures and provide further evidence that space-relevant radiation exposures disrupt critical cognitive processes and underlying neuronal network-level plasticity, albeit not to the extent that might have been previously predicted. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00018-022-04666-8. |
format | Online Article Text |
id | pubmed-9823026 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-98230262023-01-08 Galactic cosmic radiation exposure causes multifaceted neurocognitive impairments Alaghband, Yasaman Klein, Peter M. Kramár, Eniko A. Cranston, Michael N. Perry, Bayley C. Shelerud, Lukas M. Kane, Alice E. Doan, Ngoc-Lien Ru, Ning Acharya, Munjal M. Wood, Marcelo A. Sinclair, David A. Dickstein, Dara L. Soltesz, Ivan Limoli, Charles L. Baulch, Janet E. Cell Mol Life Sci Original Article Technological advancements have facilitated the implementation of realistic, terrestrial-based complex 33-beam galactic cosmic radiation simulations (GCR Sim) to now probe central nervous system functionality. This work expands considerably on prior, simplified GCR simulations, yielding new insights into responses of male and female mice exposed to 40–50 cGy acute or chronic radiations relevant to deep space travel. Results of the object in updated location task suggested that exposure to acute or chronic GCR Sim induced persistent impairments in hippocampus-dependent memory formation and reconsolidation in female mice that did not manifest robustly in irradiated male mice. Interestingly, irradiated male mice, but not females, were impaired in novel object recognition and chronically irradiated males exhibited increased aggressive behavior on the tube dominance test. Electrophysiology studies used to evaluate synaptic plasticity in the hippocampal CA1 region revealed significant reductions in long-term potentiation after each irradiation paradigm in both sexes. Interestingly, network-level disruptions did not translate to altered intrinsic electrophysiological properties of CA1 pyramidal cells, whereas acute exposures caused modest drops in excitatory synaptic signaling in males. Ultrastructural analyses of CA1 synapses found smaller postsynaptic densities in larger spines of chronically exposed mice compared to controls and acutely exposed mice. Myelination was also affected by GCR Sim with acutely exposed mice exhibiting an increase in the percent of myelinated axons; however, the myelin sheathes on small calibur (< 0.3 mm) and larger (> 0.5 mm) axons were thinner when compared to controls. Present findings might have been predicted based on previous studies using single and mixed beam exposures and provide further evidence that space-relevant radiation exposures disrupt critical cognitive processes and underlying neuronal network-level plasticity, albeit not to the extent that might have been previously predicted. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00018-022-04666-8. Springer International Publishing 2023-01-06 2023 /pmc/articles/PMC9823026/ /pubmed/36607431 http://dx.doi.org/10.1007/s00018-022-04666-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 | Original Article Alaghband, Yasaman Klein, Peter M. Kramár, Eniko A. Cranston, Michael N. Perry, Bayley C. Shelerud, Lukas M. Kane, Alice E. Doan, Ngoc-Lien Ru, Ning Acharya, Munjal M. Wood, Marcelo A. Sinclair, David A. Dickstein, Dara L. Soltesz, Ivan Limoli, Charles L. Baulch, Janet E. Galactic cosmic radiation exposure causes multifaceted neurocognitive impairments |
title | Galactic cosmic radiation exposure causes multifaceted neurocognitive impairments |
title_full | Galactic cosmic radiation exposure causes multifaceted neurocognitive impairments |
title_fullStr | Galactic cosmic radiation exposure causes multifaceted neurocognitive impairments |
title_full_unstemmed | Galactic cosmic radiation exposure causes multifaceted neurocognitive impairments |
title_short | Galactic cosmic radiation exposure causes multifaceted neurocognitive impairments |
title_sort | galactic cosmic radiation exposure causes multifaceted neurocognitive impairments |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9823026/ https://www.ncbi.nlm.nih.gov/pubmed/36607431 http://dx.doi.org/10.1007/s00018-022-04666-8 |
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