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Neural Correlates of Vestibular Processing During a Spaceflight Analog With Elevated Carbon Dioxide (CO(2)): A Pilot Study

Astronauts return to Earth from spaceflight missions with impaired mobility and balance; recovery can last weeks postflight. This is due in large part to the altered vestibular signaling and sensory reweighting that occurs in microgravity. The neural mechanisms of spaceflight-induced vestibular chan...

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Autores principales: Hupfeld, Kathleen E., Lee, Jessica K., Gadd, Nichole E., Kofman, Igor S., De Dios, Yiri E., Bloomberg, Jacob J., Mulavara, Ajitkumar P., Seidler, Rachael D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6965349/
https://www.ncbi.nlm.nih.gov/pubmed/31998084
http://dx.doi.org/10.3389/fnsys.2019.00080
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author Hupfeld, Kathleen E.
Lee, Jessica K.
Gadd, Nichole E.
Kofman, Igor S.
De Dios, Yiri E.
Bloomberg, Jacob J.
Mulavara, Ajitkumar P.
Seidler, Rachael D.
author_facet Hupfeld, Kathleen E.
Lee, Jessica K.
Gadd, Nichole E.
Kofman, Igor S.
De Dios, Yiri E.
Bloomberg, Jacob J.
Mulavara, Ajitkumar P.
Seidler, Rachael D.
author_sort Hupfeld, Kathleen E.
collection PubMed
description Astronauts return to Earth from spaceflight missions with impaired mobility and balance; recovery can last weeks postflight. This is due in large part to the altered vestibular signaling and sensory reweighting that occurs in microgravity. The neural mechanisms of spaceflight-induced vestibular changes are not well understood. Head-down-tilt bed rest (HDBR) is a common spaceflight analog environment that allows for study of body unloading, fluid shifts, and other consequences of spaceflight. Subjects in this context still show vestibular changes despite being in Earth’s gravitational environment, potentially due to sensory reweighting. Previously, we found evidence of sensory reweighting and reduced neural efficiency for vestibular processing in subjects who underwent a 70-day HDBR intervention. Here we extend this work by evaluating the impact of HDBR paired with elevated carbon dioxide (CO(2)) to mimic International Space Station conditions on vestibular neural processing. Eleven participants (6 males, 34 ± 8 years) completed 30 days of HDBR combined with 0.5% atmospheric CO(2) (HDBR + CO(2)). Participants underwent six functional magnetic resonance imaging (fMRI) sessions pre-, during, and post- HDBR + CO(2) while we measured brain activity in response to pneumatic skull taps (a validated method of vestibular stimulation). We also measured mobility and balance performance several times before and after the intervention. We found support for adaptive neural changes within the vestibular system during bed rest that subsequently recovered in several cortical and cerebellar regions. Further, there were multiple brain regions where greater pre- to post- deactivation was associated with reduced pre- to post- balance declines. That is, increased deactivation of certain brain regions associated with better balance post-HDBR + CO(2). We also found that, compared to HDBR alone (n = 13 males; 29 ± 3 years) HDBR + CO(2) is associated with greater increases in activation of multiple frontal, parietal, and temporal regions during vestibular stimulation. This suggests interactive or additive effects of bed rest and elevated CO(2). Finally, we found stronger correlations between pre- to post- HDBR + CO(2) brain changes and dependence on the visual system during balance for subjects who developed signs of Spaceflight-Associated Neuro-ocular Syndrome (SANS). Together, these findings have clear implications for understanding the neural mechanisms of bed rest and spaceflight-related changes in vestibular processing, as well as adaptation to altered sensory inputs.
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spelling pubmed-69653492020-01-29 Neural Correlates of Vestibular Processing During a Spaceflight Analog With Elevated Carbon Dioxide (CO(2)): A Pilot Study Hupfeld, Kathleen E. Lee, Jessica K. Gadd, Nichole E. Kofman, Igor S. De Dios, Yiri E. Bloomberg, Jacob J. Mulavara, Ajitkumar P. Seidler, Rachael D. Front Syst Neurosci Neuroscience Astronauts return to Earth from spaceflight missions with impaired mobility and balance; recovery can last weeks postflight. This is due in large part to the altered vestibular signaling and sensory reweighting that occurs in microgravity. The neural mechanisms of spaceflight-induced vestibular changes are not well understood. Head-down-tilt bed rest (HDBR) is a common spaceflight analog environment that allows for study of body unloading, fluid shifts, and other consequences of spaceflight. Subjects in this context still show vestibular changes despite being in Earth’s gravitational environment, potentially due to sensory reweighting. Previously, we found evidence of sensory reweighting and reduced neural efficiency for vestibular processing in subjects who underwent a 70-day HDBR intervention. Here we extend this work by evaluating the impact of HDBR paired with elevated carbon dioxide (CO(2)) to mimic International Space Station conditions on vestibular neural processing. Eleven participants (6 males, 34 ± 8 years) completed 30 days of HDBR combined with 0.5% atmospheric CO(2) (HDBR + CO(2)). Participants underwent six functional magnetic resonance imaging (fMRI) sessions pre-, during, and post- HDBR + CO(2) while we measured brain activity in response to pneumatic skull taps (a validated method of vestibular stimulation). We also measured mobility and balance performance several times before and after the intervention. We found support for adaptive neural changes within the vestibular system during bed rest that subsequently recovered in several cortical and cerebellar regions. Further, there were multiple brain regions where greater pre- to post- deactivation was associated with reduced pre- to post- balance declines. That is, increased deactivation of certain brain regions associated with better balance post-HDBR + CO(2). We also found that, compared to HDBR alone (n = 13 males; 29 ± 3 years) HDBR + CO(2) is associated with greater increases in activation of multiple frontal, parietal, and temporal regions during vestibular stimulation. This suggests interactive or additive effects of bed rest and elevated CO(2). Finally, we found stronger correlations between pre- to post- HDBR + CO(2) brain changes and dependence on the visual system during balance for subjects who developed signs of Spaceflight-Associated Neuro-ocular Syndrome (SANS). Together, these findings have clear implications for understanding the neural mechanisms of bed rest and spaceflight-related changes in vestibular processing, as well as adaptation to altered sensory inputs. Frontiers Media S.A. 2020-01-10 /pmc/articles/PMC6965349/ /pubmed/31998084 http://dx.doi.org/10.3389/fnsys.2019.00080 Text en Copyright © 2020 Hupfeld, Lee, Gadd, Kofman, De Dios, Bloomberg, Mulavara and Seidler. http://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
Hupfeld, Kathleen E.
Lee, Jessica K.
Gadd, Nichole E.
Kofman, Igor S.
De Dios, Yiri E.
Bloomberg, Jacob J.
Mulavara, Ajitkumar P.
Seidler, Rachael D.
Neural Correlates of Vestibular Processing During a Spaceflight Analog With Elevated Carbon Dioxide (CO(2)): A Pilot Study
title Neural Correlates of Vestibular Processing During a Spaceflight Analog With Elevated Carbon Dioxide (CO(2)): A Pilot Study
title_full Neural Correlates of Vestibular Processing During a Spaceflight Analog With Elevated Carbon Dioxide (CO(2)): A Pilot Study
title_fullStr Neural Correlates of Vestibular Processing During a Spaceflight Analog With Elevated Carbon Dioxide (CO(2)): A Pilot Study
title_full_unstemmed Neural Correlates of Vestibular Processing During a Spaceflight Analog With Elevated Carbon Dioxide (CO(2)): A Pilot Study
title_short Neural Correlates of Vestibular Processing During a Spaceflight Analog With Elevated Carbon Dioxide (CO(2)): A Pilot Study
title_sort neural correlates of vestibular processing during a spaceflight analog with elevated carbon dioxide (co(2)): a pilot study
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6965349/
https://www.ncbi.nlm.nih.gov/pubmed/31998084
http://dx.doi.org/10.3389/fnsys.2019.00080
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