Evidence map›Paper›PMID 40138271›Full record

ArticlePloS one2025

37-Day microgravity exposure in 16-Week female C57BL/6J mice is associated with bone loss specific to weight-bearing skeletal sites.

Rukmani Cahill, Elizabeth A Blaber, Cassandra M Juran, Margareth Cheng-Campbell, Joshua S Alwood, Yasaman Shirazi-Fard, Eduardo A C Almeida

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Rukmani CahillBlue Marble Space Institute of Science, Seattle, Washington, United States of America.
Elizabeth A BlaberBlue Marble Space Institute of Science, Seattle, Washington, United States of America.
Cassandra M JuranBlue Marble Space Institute of Science, Seattle, Washington, United States of America.
Margareth Cheng-CampbellBlue Marble Space Institute of Science, Seattle, Washington, United States of America.
Joshua S AlwoodSpace Biosciences Division, NASA Ames Research Center, Moffett Field, California, United States of America.
Yasaman Shirazi-FardSpace Biosciences Division, NASA Ames Research Center, Moffett Field, California, United States of America.
Eduardo A C AlmeidaSpace Biosciences Division, NASA Ames Research Center, Moffett Field, California, United States of America.ORCID 0000-0002-3420-6651

Funding

NASA NNH14ZTT001N14-14SF
6 · The paper itself

Abstract

Exposure to weightlessness in microgravity and elevated space radiation are associated with rapid bone loss in mammals, but questions remain about their mechanisms of action and relative importance. In this study, we tested the hypothesis that bone loss during spaceflight in Low Earth Orbit is primarily associated with site-specific microgravity unloading of weight-bearing sites in the skeleton. Microcomputed tomography and histological analyses of bones from mice space flown on ISS for 37 days in the NASA Rodent Research-1 experiment show significant site-specific cancellous and cortical bone loss occurring in the femur, but not in L2 vertebrae. The lack of bone degenerative effects in the spine in combination with same-animal paired losses in the femur suggests that space radiation levels in Low Earth Orbit or other systemic stresses are not likely to significantly contribute to the observed bone loss. Remarkably, spaceflight is also associated with accelerated progression of femoral head endochondral ossification. This suggests the microgravity environment promotes premature progression of secondary ossification during late stages of skeletal maturation at 21 weeks. Furthermore, mice housed in the NASA ISS Rodent Habitat during 1g ground controls maintained or gained bone relative to mice housed in standard vivarium cages that showed significant bone mass declines. These findings suggest that housing in the Rodent Habitat with greater topological enrichment from 3D wire-mesh surfaces may promote increased mechanical loading of weight-bearing bones and maintenance of bone mass. In summary, our results indicate that in female mice approaching skeletal maturity, mechanical unloading of weight-bearing sites is the major cause of bone loss in microgravity, while sites loaded predominantly by muscle activity, such as the spine, appear unaffected. Additionally, we identified early-onset of femoral head epiphyseal plate secondary ossification as a novel spaceflight skeletal unloading effect that may lead to premature long bone growth arrest in microgravity.

Indexed as

Weight-BearingWeightlessnessAnimalsFemaleFemurMiceMice, Inbred C57BLOsteogenesisSpace FlightX-Ray Microtomography

Identifiers

PMID40138271
PMCPMC11940681

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.