Cited by 108Spaceflight effects on biologyMetabolomics and Mass Spectrometry StudiesLiver Disease Diagnosis and Treatment

Spaceflight Activates Lipotoxic Pathways in Mouse Liver

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Jonscher, Karen R., Alfonso-Garcia, Alba, Suhalim, Jeffrey L., Orlicky, David J., Potma, Eric O., Ferguson, Virginia L., Bouxsein, Mary L., Bateman, Ted A. +5 more·2016·PLOS ONE

Abstract

Spaceflight affects numerous organ systems in the body, leading to metabolic dysfunction that may have long-term consequences. Microgravity-induced alterations in liver metabolism, particularly with respect to lipids, remain largely unexplored. Here we utilize a novel systems biology approach, combining metabolomics and transcriptomics with advanced Raman microscopy, to investigate altered hepatic lipid metabolism in mice following short duration spaceflight. Mice flown aboard Space Transportation System -135, the last Shuttle mission, lose weight but redistribute lipids, particularly to the liver. Intriguingly, spaceflight mice lose retinol from lipid droplets. Both mRNA and metabolite changes suggest the retinol loss is linked to activation of PPARα-mediated pathways and potentially to hepatic stellate cell activation, both of which may be coincident with increased bile acids and early signs of liver injury. Although the 13-day flight duration is too short for frank fibrosis to develop, the retinol loss plus changes in markers of extracellular matrix remodeling raise the concern that longer duration exposure to the space environment may result in progressive liver damage, increasing the risk for nonalcoholic fatty liver disease.

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  • Mice aboard the Space Transportation System (STS)-135 had liver damage due to increased liver lipid drops, elevated triglyceride levels, and loss of retinoids from lipid drops of liver stellate cells.

    “Interestingly, it was shown that mice aboard the Space Transportation System (STS)-135 had liver damage due to increased liver lipid drops, elevated triglyceride levels, and loss of retinoids from lipid drops of liver stellate cells75.”

    From Key points for the development of antioxidant cocktails to prevent cellular stress and damage caused by reactive oxygen species (ROS) during manned space missions (2021) · cites this paper as [75]

    The Results report increased hepatic lipid storage and elevated total triglycerides, and the Conclusions report loss of retinoids from hepatic stellate-cell lipid droplets. But the Introduction and Abstract describe early signs of liver injury and a concern about future damage, not established liver damage caused by those changes. (LLM, conf=0.88)

    Experimental — accuracy not yet measured
  • Pro-inflammatory responses negatively regulate PPARα in rodent models of atherosclerosis and early NAFLD, which could be affecting astronauts as well.

    “Pro-inflammatory responses negatively regulate PPARα in rodent models of atherosclerosis and early NAFLD that could be affecting astronauts as well75,76,79,80.”

    From Key points for the development of antioxidant cocktails to prevent cellular stress and damage caused by reactive oxygen species (ROS) during manned space missions (2021) · cites this paper as [75]

    The Introduction describes pro-inflammatory cytokines in NAFLD, and the Conclusions suggest that spaceflight may lead to early NAFLD with implications for astronaut health. But the paper does not say that inflammation negatively regulates PPARα in rodent models of atherosclerosis or early NAFLD; its Results instead report activation of PPARα pathways in spaceflight mice. (LLM, conf=0.82)

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Authors
Jonscher, K. R., Alfonso-Garcia, A., Suhalim, J. L., Orlicky, D. J., Potma, E. O., Ferguson, V. L., Bouxsein, M. L., Bateman, T. A., Stodieck, L. S., Levi, M., Friedman, J. E., Gridley, D. S., & Pecaut, M. J.
Affiliations
  • University of Colorado Anschutz (US)
  • University of California, Irvine (US)
  • University of Colorado Boulder (US)
  • Harvard University (US)
  • University of North Carolina at Chapel Hill (US)
  • Loma Linda University Medical Center (US)
Corresponding author
Jonscher, Karen R.
Venue
PLOS ONE
Published
2016-04-20
Volume
11
Issue
4
Pages
e0152877
ISSN
1932-6203 (ISSN-L)
OpenAlex
W2339163193
Cited by
108
References
3
Citations by year
2026: 8 · 2025: 12 · 2024: 15 · 2023: 12 · 2022: 9 · 2021: 8 · 2020: 13 · 2019: 9 · 2018: 14 · 2017: 6 · 2016: 2
FWCI
8.32
Type
journal article
Language
en
Open access
Locations
  • PLoS ONE (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • Carolina Digital Repository (University of North Carolina at Chapel Hill) (submittedVersion, other-oa)
  • CU Scholar (University of Colorado Boulder) (submittedVersion)
  • Digital Access to Scholarship at Harvard (DASH) (Harvard University) (submittedVersion, cc-by)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
  • eScholarship (California Digital Library) (submittedVersion)
  • eScholarship (California Digital Library) (submittedVersion, cc-by)
  • Figshare (submittedVersion, cc-by)
  • UNC Libraries
Funders
  • National Aeronautics and Space Administration (NNX10AJ31G, NNX10AE39G)
  • Amgen
  • Kennedy Space Center
  • University of Colorado Denver
  • Anschutz Medical Campus, University of Colorado
Topics
  • Health Sciences › Medicine › Physiology › Spaceflight effects on biology
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolomics and Mass Spectrometry Studies
  • Health Sciences › Medicine › Epidemiology › Liver Disease Diagnosis and Treatment
Keywords
spaceflight, microgravity, hepatic lipid metabolism, lipotoxicity, retinol, lipid droplets, PPARα, hepatic stellate cells, bile acids, liver injury, extracellular matrix remodeling, non-alcoholic fatty liver disease, mouse liver
MeSH terms
Animals, Body Weight, Female, Liver, Mice, Inbred C57BL, RNA, Messenger, Space Flight, Biomarkers, Gene Expression Profiling, PPAR alpha, Systems Biology, Mice, Hepatic Stellate Cells, Metabolomics, Lipid Droplets

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