Evidence map›Paper›PMID 39763085›Full record

ArticleMedicine and science in sports and exercise2025

Acute and Lifelong Endurance Exercise Yields Differential Effects During Circadian Disruption in Mice.

Cole F Nelson, Cole R Wyatt, Evan C Johnson, William D Todd, Emily E Schmitt

Abstract read
In one paragraph

Article in Medicine and science in sports and exercise, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

0 citing papers in PubMed.

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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

5 authors.

Cole F NelsonDivision of Kinesiology and Health, University of Wyoming, Laramie, WY.
Cole R WyattDivision of Kinesiology and Health, University of Wyoming, Laramie, WY.
Evan C JohnsonDivision of Kinesiology and Health, University of Wyoming, Laramie, WY.
William D ToddDepartment of Zoology and Physiology, Program in Neuroscience, University of Wyoming, Laramie, WY.
Emily E Schmitt

Funding

Wyoming INBRE Phase 4- Equipment Supplement for x-ray diffractometer for Center for Advanced Scientific InstrumentationP20GM103432 · NIGMS · UNIVERSITY OF WYOMING · PI Nicolas A. Blouin · 2012 to 2026
$56.8M
Zebrafish Models of CNS Injury and Locomotor RecoveryP20GM121310 · NIGMS · UNIVERSITY OF WYOMING · PI Qian-Quan Sun · 2017 to 2026
$27.2M
NIGMS NIH HHS P20 GM103432NIGMS NIH HHS P20 GM121310
6 · The paper itself

Abstract

introductionCircadian rhythms are responsible for physiological and behavioral processes coordinated in a 24-h cycle. We investigated whether untimed, long-term voluntary wheel access mitigated circadian disruption and facilitated re-entrainment.

methodsThirty-five C57Bl/6J mice ( n = 21 males, n = 14 females) were used in this experiment. Long-term exercised (LTEx) mice ran from 3 wk to 12 months of age. At 12 months, animals were circadian disrupted for 14 d and then re-entrained for 7 d. Long-term sedentary (LTSed) animals were disrupted but had no access to a wheel. Another long-term sedentary group had access to a wheel only during disruption (LTSed+Ex). SubCue data loggers were used to track internal rhythm of core body temperature (Tb). RNA was extracted from skeletal muscle and RT-qPCR was used to analyze gene expression.

resultsOverall, all three experimental groups had an initial entrained period lengths of ~24 h at baseline. There was a main effect of time ( P = 0.012), treatment ( P = 0.005), and time-treatment interaction ( P = 0.033) from baseline to disruption. A post hoc analysis within-group one-way ANOVA showed no difference between baseline and disruption period lengths in the LTSed+Ex treatment, yet a difference from baseline to disruption in LTSed and LTEx. Lastly, there is a difference in entrained period lengths between all three treatment groups at the re-entrainment time point ( P = 0.026) with a difference in change between disruption and re-entrainment with LTEx being lower than LTSed+Ex.

conclusionsOur results suggest that acute-like exercise during circadian disruption aided in mitigating circadian disruption. When all treatment groups were re-entrained back to a normal rhythm, the LTEx animals that had access to a wheel before, during, and after disruption had period lengths closest to baseline values.

Indexed as

Circadian RhythmPhysical Conditioning, AnimalPhysical EnduranceAnimalsBody TemperatureFemaleMaleMiceMice, Inbred C57BLMuscle, SkeletalCIRCADIAN RHYTHMPHYSICAL ACTIVITYWHEEL RUNNING

Identifiers

PMID39763085
PMCPMC12081177

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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.