Evidence map›Paper›PMID 39605860›Full record

ArticleFrontiers in physiology2024

Effects of 5-ion 6-beam sequential irradiation in the presence and absence of hindlimb or control hindlimb unloading on behavioral performances and plasma metabolic pathways of Fischer 344 rats.

Jacob Raber, Mitali Chaudhari, Alexis De la Torre, Sarah Holden, Kat Kessler, Breanna Glaeser, Marek Lenarczyk, Scott Willem Leonard, Alexander Borg, Andy Kwok and 10 more

Abstract read
In one paragraph

Article in Frontiers in physiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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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

2 citing papers in PubMed.

  1. Article
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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

20 authors.

Jacob RaberDepartment of Behavioral Neuroscience, Oregon Health & Science University, Portland, OR, United States.
Mitali ChaudhariDepartment of Behavioral Neuroscience, Oregon Health & Science University, Portland, OR, United States.
Alexis De la TorreDepartment of Behavioral Neuroscience, Oregon Health & Science University, Portland, OR, United States.
Sarah HoldenDepartment of Behavioral Neuroscience, Oregon Health & Science University, Portland, OR, United States.
Kat KesslerDepartment of Behavioral Neuroscience, Oregon Health & Science University, Portland, OR, United States.
Breanna GlaeserNeuroscience Center and Department of Pharmacology and Toxicology, Medical College of Wisconsin, Milwaukee, WI, United States.
Marek LenarczykRadiation Biosciences laboratory, Medical College of Wisconsin, Milwaukee, WI, United States.
Scott Willem LeonardDepartment of Radiation Oncology, Wake Forest School of Medicine, Winston-Salem, NC, United States.
Alexander BorgDepartment of Radiation Oncology, Wake Forest School of Medicine, Winston-Salem, NC, United States.
Andy KwokDepartment of Radiation Oncology, Wake Forest School of Medicine, Winston-Salem, NC, United States.
Chirayu PatelDepartment of Radiation Oncology, Wake Forest School of Medicine, Winston-Salem, NC, United States.
Amy KronenbergBiological Systems and Engineering Division, Lawrence Berkeley National Laboratory, Berkeley, CA, United States.
Christopher M OlsenNeuroscience Center and Department of Pharmacology and Toxicology, Medical College of Wisconsin, Milwaukee, WI, United States.
Jeffrey S WilleyDepartment of Radiation Oncology, Wake Forest School of Medicine, Winston-Salem, NC, United States.
Jeffrey MorréMass Spectrometry Center, Oregon State University, Corvallis, OR, United States.
Jaewoo ChoiMass Spectrometry Center, Oregon State University, Corvallis, OR, United States.
Jan Frederik StevensCollege of Pharmacy, Oregon State University, Corvallis, OR, United States.
Gerd BobeLinus Pauling Institute, Oregon State University, Corvallis, OR, United States.
Jessica MinnierDepartment of Behavioral Neuroscience, Oregon Health & Science University, Portland, OR, United States.
John BakerRadiation Biosciences laboratory, Medical College of Wisconsin, Milwaukee, WI, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Effects and interactions between different spaceflight stressors are expected to be experienced by crew on missions when exposed to microgravity and galactic cosmic rays (GCRs). One of the limitations of previous studies on simulated weightlessness using hindlimb unloading (HU) is that a control HU condition was not included. Methods: We characterized the behavioral performance of male Fischer rats 2 months after sham or total body irradiation with a simplified 5-ion 6-mixed-beam exposure representative of GCRs in the absence or presence of HU. Six months later, the plasma, hippocampus, and cortex were processed to determine whether the behavioral effects were associated with long-term alterations in the metabolic pathways. Results: In the open field without and with objects, interactions were observed for radiation × HU. In the plasma of animals that were not under the HU or control HU condition, the riboflavin metabolic pathway was affected most for sham irradiation vs. 0.75 Gy exposure. Analysis of the effects of control HU on plasma in the sham-irradiated animals showed that the alanine, aspartate, glutamate, riboflavin, and glutamine metabolisms as well as arginine biosynthesis were affected. The effects of control HU on the hippocampus in the sham-irradiated animals showed that the phenylalanine, tyrosine, and tryptophan pathway was affected the most. Analysis of effects of 0.75 Gy irradiation on the cortex of control HU animals showed that the glutamine and glutamate metabolic pathway was affected similar to the hippocampus, while the riboflavin pathway was affected in animals that were not under the control HU condition. The effects of control HU on the cortex in sham-irradiated animals showed that the riboflavin metabolic pathway was affected. Animals receiving 0.75 Gy of irradiation showed impaired glutamine and glutamate metabolic pathway, whereas animals receiving 1.5 Gy of irradiation showed impaired riboflavin metabolic pathways. A total of 21 plasma metabolites were correlated with the behavioral measures, indicating that plasma and brain biomarkers associated with behavioral performance are dependent on the environmental conditions experienced. Discussion: Phenylalanine, tyrosine, and tryptophan metabolism as well as phenylalanine and tryptophan as plasma metabolites are biomarkers that can be considered for spaceflight as they were revealed in both Fischer and WAG/Rij rats exposed to simGCRsim and/or HU.

Indexed as

5-ion beam irradiationFischer ratshindlimb unloadingmetabolomicsobject recognitionopen-field

Identifiers

PMID39605860
PMCPMC11598337

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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.