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“Monitoring inflammatory, immune system mediators, and mitochondrial changes related to brain metabolism during space flight”

  • Darcy Tocci
  • , Tomas Ducai
  • , C. A.Barry Stoute
  • , Gabrielle Hopkins
  • , Mohammad G. Sabbir
  • , Afshin Beheshti
  • , Benedict C. Albensi

Research output: Contribution to journal › Review article › peer-review

Abstract

The possibility of impaired cognitive function during deep space flight missions or while living on a Martian colony is a critical point of concern and pleads for further research. In addition, a fundamental gap exists both in our understanding and application of countermeasures for the consequences of long duration space travel and/or living in an extreme environment such as on the Moon or Mars. Previous studies, while heavily analyzing pre- and post-flight conditions, mostly fail to appreciate the cognitive stressors associated with space radiation, microgravity, confinement, hostile or closed environments, and the long distances from earth. A specific understanding of factors that affect cognition as well as structural and/or physiological changes in the brains of those on a space mission in addition to new countermeasures should result in improved health of our astronauts and reduce risks. At the core of cognitive changes are mechanisms we typically associate with aging, such as inflammatory responses, changes in brain metabolism, depression, and memory impairments. In fact, space flight appears to accelerate aging. In this review, we will discuss the importance of monitoring inflammatory and immune system mediators such as nuclear factor kappa B (NF-κB), and mitochondrial changes related to brain metabolism. We conclude with our recommended countermeasures that include pharmacological, metabolic, and nutritional considerations for the risks on cognition during space missions.

Original languageEnglish
Article number1422864
JournalFrontiers in Immunology
Volume15
DOIs
StatePublished - Oct 1 2024

Bibliographical note

Copyright © 2024 Tocci, Ducai, Stoute, Hopkins, Sabbir, Beheshti and Albensi.

Funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. Additional funding for research related to aging, inflammation, neurodegeneration, and mitochondrial dysfunction to BA received from NIH 1R16NS134540-01 and CIHR PJT-162144.

FundersFunder number
National Institutes of Health1R16NS134540-01, CIHR PJT-162144

    ASJC Scopus Subject Areas

    • Immunology and Allergy
    • Immunology

    Keywords

    • aging
    • brain
    • CNS
    • cognition
    • countermeasures
    • memory
    • space flight
    • space medicine
    • Inflammation Mediators/metabolism
    • Mitochondria/metabolism
    • Humans
    • Weightlessness/adverse effects
    • Cognition
    • Space Flight
    • Inflammation/immunology
    • Animals
    • Brain/metabolism

    Disciplines

    • Medical Immunology
    • Allergy and Immunology

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