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Multi-Domain Touchscreen-Based Cognitive Assessment of C57BL/6J Female Mice Shows Whole-Body Exposure to (56)Fe Particle Space Radiation in Maturity Improves Discrimination Learning Yet Impairs Stimulus-Response Rule-Based Habit Learning

Astronauts during interplanetary missions will be exposed to galactic cosmic radiation, including charged particles like (56)Fe. Most preclinical studies with mature, “astronaut-aged” rodents suggest space radiation diminishes performance in classical hippocampal- and prefrontal cortex-dependent tas...

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Autores principales: Soler, Ivan, Yun, Sanghee, Reynolds, Ryan P., Whoolery, Cody W., Tran, Fionya H., Kumar, Priya L., Rong, Yuying, DeSalle, Matthew J., Gibson, Adam D., Stowe, Ann M., Kiffer, Frederico C., Eisch, Amelia J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8543003/
https://www.ncbi.nlm.nih.gov/pubmed/34707486
http://dx.doi.org/10.3389/fnbeh.2021.722780
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author Soler, Ivan
Yun, Sanghee
Reynolds, Ryan P.
Whoolery, Cody W.
Tran, Fionya H.
Kumar, Priya L.
Rong, Yuying
DeSalle, Matthew J.
Gibson, Adam D.
Stowe, Ann M.
Kiffer, Frederico C.
Eisch, Amelia J.
author_facet Soler, Ivan
Yun, Sanghee
Reynolds, Ryan P.
Whoolery, Cody W.
Tran, Fionya H.
Kumar, Priya L.
Rong, Yuying
DeSalle, Matthew J.
Gibson, Adam D.
Stowe, Ann M.
Kiffer, Frederico C.
Eisch, Amelia J.
author_sort Soler, Ivan
collection PubMed
description Astronauts during interplanetary missions will be exposed to galactic cosmic radiation, including charged particles like (56)Fe. Most preclinical studies with mature, “astronaut-aged” rodents suggest space radiation diminishes performance in classical hippocampal- and prefrontal cortex-dependent tasks. However, a rodent cognitive touchscreen battery unexpectedly revealed (56)Fe radiation improves the performance of C57BL/6J male mice in a hippocampal-dependent task (discrimination learning) without changing performance in a striatal-dependent task (rule-based learning). As there are conflicting results on whether the female rodent brain is preferentially injured by or resistant to charged particle exposure, and as the proportion of female vs. male astronauts is increasing, further study on how charged particles influence the touchscreen cognitive performance of female mice is warranted. We hypothesized that, similar to mature male mice, mature female C57BL/6J mice exposed to fractionated whole-body (56)Fe irradiation (3 × 6.7cGy (56)Fe over 5 days, 600 MeV/n) would improve performance vs. Sham conditions in touchscreen tasks relevant to hippocampal and prefrontal cortical function [e.g., location discrimination reversal (LDR) and extinction, respectively]. In LDR, (56)Fe female mice more accurately discriminated two discrete conditioned stimuli relative to Sham mice, suggesting improved hippocampal function. However, (56)Fe and Sham female mice acquired a new simple stimulus-response behavior and extinguished this acquired behavior at similar rates, suggesting similar prefrontal cortical function. Based on prior work on multiple memory systems, we next tested whether improved hippocampal-dependent function (discrimination learning) came at the expense of striatal stimulus-response rule-based habit learning (visuomotor conditional learning). Interestingly, (56)Fe female mice took more days to reach criteria in this striatal-dependent rule-based test relative to Sham mice. Together, our data support the idea of competition between memory systems, as an (56)Fe-induced decrease in striatal-based learning is associated with enhanced hippocampal-based learning. These data emphasize the power of using a touchscreen-based battery to advance our understanding of the effects of space radiation on mission critical cognitive function in females, and underscore the importance of preclinical space radiation risk studies measuring multiple cognitive processes, thereby preventing NASA’s risk assessments from being based on a single cognitive domain.
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spelling pubmed-85430032021-10-26 Multi-Domain Touchscreen-Based Cognitive Assessment of C57BL/6J Female Mice Shows Whole-Body Exposure to (56)Fe Particle Space Radiation in Maturity Improves Discrimination Learning Yet Impairs Stimulus-Response Rule-Based Habit Learning Soler, Ivan Yun, Sanghee Reynolds, Ryan P. Whoolery, Cody W. Tran, Fionya H. Kumar, Priya L. Rong, Yuying DeSalle, Matthew J. Gibson, Adam D. Stowe, Ann M. Kiffer, Frederico C. Eisch, Amelia J. Front Behav Neurosci Neuroscience Astronauts during interplanetary missions will be exposed to galactic cosmic radiation, including charged particles like (56)Fe. Most preclinical studies with mature, “astronaut-aged” rodents suggest space radiation diminishes performance in classical hippocampal- and prefrontal cortex-dependent tasks. However, a rodent cognitive touchscreen battery unexpectedly revealed (56)Fe radiation improves the performance of C57BL/6J male mice in a hippocampal-dependent task (discrimination learning) without changing performance in a striatal-dependent task (rule-based learning). As there are conflicting results on whether the female rodent brain is preferentially injured by or resistant to charged particle exposure, and as the proportion of female vs. male astronauts is increasing, further study on how charged particles influence the touchscreen cognitive performance of female mice is warranted. We hypothesized that, similar to mature male mice, mature female C57BL/6J mice exposed to fractionated whole-body (56)Fe irradiation (3 × 6.7cGy (56)Fe over 5 days, 600 MeV/n) would improve performance vs. Sham conditions in touchscreen tasks relevant to hippocampal and prefrontal cortical function [e.g., location discrimination reversal (LDR) and extinction, respectively]. In LDR, (56)Fe female mice more accurately discriminated two discrete conditioned stimuli relative to Sham mice, suggesting improved hippocampal function. However, (56)Fe and Sham female mice acquired a new simple stimulus-response behavior and extinguished this acquired behavior at similar rates, suggesting similar prefrontal cortical function. Based on prior work on multiple memory systems, we next tested whether improved hippocampal-dependent function (discrimination learning) came at the expense of striatal stimulus-response rule-based habit learning (visuomotor conditional learning). Interestingly, (56)Fe female mice took more days to reach criteria in this striatal-dependent rule-based test relative to Sham mice. Together, our data support the idea of competition between memory systems, as an (56)Fe-induced decrease in striatal-based learning is associated with enhanced hippocampal-based learning. These data emphasize the power of using a touchscreen-based battery to advance our understanding of the effects of space radiation on mission critical cognitive function in females, and underscore the importance of preclinical space radiation risk studies measuring multiple cognitive processes, thereby preventing NASA’s risk assessments from being based on a single cognitive domain. Frontiers Media S.A. 2021-10-11 /pmc/articles/PMC8543003/ /pubmed/34707486 http://dx.doi.org/10.3389/fnbeh.2021.722780 Text en Copyright © 2021 Soler, Yun, Reynolds, Whoolery, Tran, Kumar, Rong, DeSalle, Gibson, Stowe, Kiffer and Eisch. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Soler, Ivan
Yun, Sanghee
Reynolds, Ryan P.
Whoolery, Cody W.
Tran, Fionya H.
Kumar, Priya L.
Rong, Yuying
DeSalle, Matthew J.
Gibson, Adam D.
Stowe, Ann M.
Kiffer, Frederico C.
Eisch, Amelia J.
Multi-Domain Touchscreen-Based Cognitive Assessment of C57BL/6J Female Mice Shows Whole-Body Exposure to (56)Fe Particle Space Radiation in Maturity Improves Discrimination Learning Yet Impairs Stimulus-Response Rule-Based Habit Learning
title Multi-Domain Touchscreen-Based Cognitive Assessment of C57BL/6J Female Mice Shows Whole-Body Exposure to (56)Fe Particle Space Radiation in Maturity Improves Discrimination Learning Yet Impairs Stimulus-Response Rule-Based Habit Learning
title_full Multi-Domain Touchscreen-Based Cognitive Assessment of C57BL/6J Female Mice Shows Whole-Body Exposure to (56)Fe Particle Space Radiation in Maturity Improves Discrimination Learning Yet Impairs Stimulus-Response Rule-Based Habit Learning
title_fullStr Multi-Domain Touchscreen-Based Cognitive Assessment of C57BL/6J Female Mice Shows Whole-Body Exposure to (56)Fe Particle Space Radiation in Maturity Improves Discrimination Learning Yet Impairs Stimulus-Response Rule-Based Habit Learning
title_full_unstemmed Multi-Domain Touchscreen-Based Cognitive Assessment of C57BL/6J Female Mice Shows Whole-Body Exposure to (56)Fe Particle Space Radiation in Maturity Improves Discrimination Learning Yet Impairs Stimulus-Response Rule-Based Habit Learning
title_short Multi-Domain Touchscreen-Based Cognitive Assessment of C57BL/6J Female Mice Shows Whole-Body Exposure to (56)Fe Particle Space Radiation in Maturity Improves Discrimination Learning Yet Impairs Stimulus-Response Rule-Based Habit Learning
title_sort multi-domain touchscreen-based cognitive assessment of c57bl/6j female mice shows whole-body exposure to (56)fe particle space radiation in maturity improves discrimination learning yet impairs stimulus-response rule-based habit learning
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8543003/
https://www.ncbi.nlm.nih.gov/pubmed/34707486
http://dx.doi.org/10.3389/fnbeh.2021.722780
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