Brain and Behavioral Evidence for Reweighting of Vestibular Inputs with Long-Duration Spaceflight

Author:

Hupfeld K E1ORCID,McGregor H R1,Koppelmans V2,Beltran N E3,Kofman I S3,De Dios Y E3,Riascos R F4,Reuter-Lorenz P A5,Wood S J6,Bloomberg J J6,Mulavara A P6,Seidler R D17ORCID

Affiliation:

1. Department of Applied Physiology and Kinesiology, University of Florida, Gainesville, FL, USA

2. Department of Psychiatry, University of Utah, Salt Lake City, UT, USA

3. KBR, Houston, TX, USA

4. Department of Diagnostic and Interventional Imaging, University of Texas Health Science Center at Houston, Houston, TX, USA

5. Department of Psychology, University of Michigan, Ann Arbor, MI, USA

6. NASA Johnson Space Center, Houston, TX, USA

7. Norman Fixel Institute for Neurological Diseases, University of Florida, Gainesville, FL, USA

Abstract

Abstract Microgravity alters vestibular signaling. In-flight adaptation to altered vestibular afferents is reflected in post-spaceflight aftereffects, evidenced by declines in vestibularly mediated behaviors (e.g., walking/standing balance), until readaptation to Earth’s 1G environment occurs. Here we examine how spaceflight affects neural processing of applied vestibular stimulation. We used fMRI to measure brain activity in response to vestibular stimulation in 15 astronauts pre- and post-spaceflight. We also measured vestibularly-mediated behaviors, including balance, mobility, and rod-and-frame test performance. Data were collected twice preflight and four times postflight. As expected, vestibular stimulation at the preflight sessions elicited activation of the parietal opercular area (“vestibular cortex”) and deactivation of somatosensory and visual cortices. Pre- to postflight, we found widespread reductions in this somatosensory and visual cortical deactivation, supporting sensory compensation and reweighting with spaceflight. These pre- to postflight changes in brain activity correlated with changes in eyes closed standing balance, and greater pre- to postflight reductions in deactivation of the visual cortices associated with less postflight balance decline. The observed brain changes recovered to baseline values by 3 months postflight. Together, these findings provide evidence for sensory reweighting and adaptive cortical neuroplasticity with spaceflight. These results have implications for better understanding compensation and adaptation to vestibular functional disruption.

Funder

NASA Human Research Program

Natural Sciences and Engineering Research Council of Canada

National Institute on Aging

National Institute of Neurological Disorders and Stroke

National Science Foundation Graduate Research

National Space Biomedical Research Institute

National Aeronautics and Space Administration

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience

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