Evidence map›Paper›PMID 36720960›Full record

ArticleScientific reports2023

Combined space stressors induce independent behavioral deficits predicted by early peripheral blood monocytes.

Kira D A Rienecker, Katherine Grue, Maria Serena Paladini, Elma S Frias, Valentina Frattini, Mia C Borlongan, Austin Chou, Abel Torres-Espin, Karen Krukowski, Adam R Ferguson and 1 more

Abstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Review
  2. Long-term molecular effects ofNPJ microgravity · 2026
    Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
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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

11 authors.

Kira D A RieneckerDepartment of Physical Therapy and Rehabilitation Science, University of California at San Francisco, San Francisco, CA, USA.
Katherine GrueDepartment of Physical Therapy and Rehabilitation Science, University of California at San Francisco, San Francisco, CA, USA.
Maria Serena PaladiniDepartment of Physical Therapy and Rehabilitation Science, University of California at San Francisco, San Francisco, CA, USA.
Elma S FriasDepartment of Physical Therapy and Rehabilitation Science, University of California at San Francisco, San Francisco, CA, USA.
Valentina FrattiniDepartment of Physical Therapy and Rehabilitation Science, University of California at San Francisco, San Francisco, CA, USA.
Mia C BorlonganDepartment of Physical Therapy and Rehabilitation Science, University of California at San Francisco, San Francisco, CA, USA.
Austin ChouDepartment of Physical Therapy and Rehabilitation Science, University of California at San Francisco, San Francisco, CA, USA.
Abel Torres-EspinBrain and Spinal Injury Center, University of California at San Francisco, San Francisco, CA, USA.
Karen KrukowskiDepartment of Physical Therapy and Rehabilitation Science, University of California at San Francisco, San Francisco, CA, USA.
Adam R FergusonBrain and Spinal Injury Center, University of California at San Francisco, San Francisco, CA, USA.
Susanna RosiDepartment of Physical Therapy and Rehabilitation Science, University of California at San Francisco, San Francisco, CA, USA. srosi@altoslabs.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interplanetary space travel poses many hazards to the human body. To protect astronaut health and performance on critical missions, there is first a need to understand the effects of deep space hazards, including ionizing radiation, confinement, and altered gravity. Previous studies of rodents exposed to a single such stressor document significant deficits, but our study is the first to investigate possible cumulative and synergistic impacts of simultaneous ionizing radiation, confinement, and altered gravity on behavior and cognition. Our cohort was divided between 6-month-old female and male mice in group, social isolation, or hindlimb unloading housing, exposed to 0 or 50 cGy of 5 ion simplified simulated galactic cosmic radiation (GCRsim). We report interactions and independent effects of GCRsim exposure and housing conditions on behavioral and cognitive performance. Exposure to GCRsim drove changes in immune cell populations in peripheral blood collected early after irradiation, while housing conditions drove changes in blood collected at a later point. Female mice were largely resilient to deficits observed in male mice. Finally, we used principal component analysis to represent total deficits as principal component scores, which were predicted by general linear models using GCR exposure, housing condition, and early blood biomarkers.

Indexed as

Cosmic RadiationMonocytesAnimalsAstronautsCognitionFemaleHumansInfantMaleMiceSocial Isolation

Identifiers

PMID36720960
PMCPMC9889764

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.