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Long-Term Changes in Cognition and Physiology after Low-Dose (16)O Irradiation

Astronauts traveling to Mars will be exposed to high levels of ionizing radiation upon leaving low-Earth orbit. During prolonged space travel, astronauts are exposed to galactic cosmic rays (GCRs) composed of protons; oxygen molecules; and high energy, high mass charged particles. Notably, oxygen mo...

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Autores principales: Howe, Alexis, Kiffer, Frederico, Alexander, Tyler C., Sridharan, Vijayalakshmi, Wang, Jing, Ntagwabira, Fabio, Rodriguez, Analiz, Boerma, Marjan, Allen, Antiño R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6337104/
https://www.ncbi.nlm.nih.gov/pubmed/30621014
http://dx.doi.org/10.3390/ijms20010188
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author Howe, Alexis
Kiffer, Frederico
Alexander, Tyler C.
Sridharan, Vijayalakshmi
Wang, Jing
Ntagwabira, Fabio
Rodriguez, Analiz
Boerma, Marjan
Allen, Antiño R.
author_facet Howe, Alexis
Kiffer, Frederico
Alexander, Tyler C.
Sridharan, Vijayalakshmi
Wang, Jing
Ntagwabira, Fabio
Rodriguez, Analiz
Boerma, Marjan
Allen, Antiño R.
author_sort Howe, Alexis
collection PubMed
description Astronauts traveling to Mars will be exposed to high levels of ionizing radiation upon leaving low-Earth orbit. During prolonged space travel, astronauts are exposed to galactic cosmic rays (GCRs) composed of protons; oxygen molecules; and high energy, high mass charged particles. Notably, oxygen molecules can travel through the shielding of spacecraft, potentially impacting 25% of the hippocampus. The aim of the current study was to assess whether (16)O-particle radiation induced a behavioral deficit and histological changes in mice. Mice were sent to the National Aeronautics and Space Administration (NASA) Space Radiation Laboratory at Brookhaven National Laboratory and exposed to particulate (16)O radiation at doses of 0 and 0.05 Gy. Nine months after irradiation, the mice were tested for novel object recognition and in the Y-maze, after which the animals were sacrificed. The brains were then dissected along the midsagittal plane for Golgi staining. Exposure to 0.05 Gy significantly impaired novel object recognition. However, short term memory and exploratory activity in the Y-maze were not affected. Micromorphometric analysis revealed significant decreases in mushroom spine density in the dentate gyrus and cornu Ammonis-1 and -3 of the hippocampus. Sholl analysis revealed a significant decrease in dendritic complexity in the dentate gyrus. The present data provide evidence that space radiation has deleterious effects on mature neurons associated with hippocampal learning and memory.
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spelling pubmed-63371042019-01-22 Long-Term Changes in Cognition and Physiology after Low-Dose (16)O Irradiation Howe, Alexis Kiffer, Frederico Alexander, Tyler C. Sridharan, Vijayalakshmi Wang, Jing Ntagwabira, Fabio Rodriguez, Analiz Boerma, Marjan Allen, Antiño R. Int J Mol Sci Article Astronauts traveling to Mars will be exposed to high levels of ionizing radiation upon leaving low-Earth orbit. During prolonged space travel, astronauts are exposed to galactic cosmic rays (GCRs) composed of protons; oxygen molecules; and high energy, high mass charged particles. Notably, oxygen molecules can travel through the shielding of spacecraft, potentially impacting 25% of the hippocampus. The aim of the current study was to assess whether (16)O-particle radiation induced a behavioral deficit and histological changes in mice. Mice were sent to the National Aeronautics and Space Administration (NASA) Space Radiation Laboratory at Brookhaven National Laboratory and exposed to particulate (16)O radiation at doses of 0 and 0.05 Gy. Nine months after irradiation, the mice were tested for novel object recognition and in the Y-maze, after which the animals were sacrificed. The brains were then dissected along the midsagittal plane for Golgi staining. Exposure to 0.05 Gy significantly impaired novel object recognition. However, short term memory and exploratory activity in the Y-maze were not affected. Micromorphometric analysis revealed significant decreases in mushroom spine density in the dentate gyrus and cornu Ammonis-1 and -3 of the hippocampus. Sholl analysis revealed a significant decrease in dendritic complexity in the dentate gyrus. The present data provide evidence that space radiation has deleterious effects on mature neurons associated with hippocampal learning and memory. MDPI 2019-01-07 /pmc/articles/PMC6337104/ /pubmed/30621014 http://dx.doi.org/10.3390/ijms20010188 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Howe, Alexis
Kiffer, Frederico
Alexander, Tyler C.
Sridharan, Vijayalakshmi
Wang, Jing
Ntagwabira, Fabio
Rodriguez, Analiz
Boerma, Marjan
Allen, Antiño R.
Long-Term Changes in Cognition and Physiology after Low-Dose (16)O Irradiation
title Long-Term Changes in Cognition and Physiology after Low-Dose (16)O Irradiation
title_full Long-Term Changes in Cognition and Physiology after Low-Dose (16)O Irradiation
title_fullStr Long-Term Changes in Cognition and Physiology after Low-Dose (16)O Irradiation
title_full_unstemmed Long-Term Changes in Cognition and Physiology after Low-Dose (16)O Irradiation
title_short Long-Term Changes in Cognition and Physiology after Low-Dose (16)O Irradiation
title_sort long-term changes in cognition and physiology after low-dose (16)o irradiation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6337104/
https://www.ncbi.nlm.nih.gov/pubmed/30621014
http://dx.doi.org/10.3390/ijms20010188
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