Evidence map›Paper›PMID 42302962›Full record

ArticlePhysiology & behavior2026

Chronic exposure to artificial light at night dampens rhythms in locomotor activity, metabolism, and sleep in female mice.

O Hecmarie Meléndez-Fernández, James C Walton, William H Walker Ii, Jennifer A Liu, Paul D Chantler, A Courtney DeVries, Randy J Nelson

Abstract read
In one paragraph

Article in Physiology & behavior, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

O Hecmarie Meléndez-FernándezDepartment of Neuroscience, Rockefeller Neuroscience Institute, West Virginia University, Morgantown, WV 26505, USA.
James C WaltonDepartment of Neuroscience, Rockefeller Neuroscience Institute, West Virginia University, Morgantown, WV 26505, USA. Electronic address: james.walton@hsc.wvu.edu.
William H Walker IiDepartment of Neuroscience, Rockefeller Neuroscience Institute, West Virginia University, Morgantown, WV 26505, USA.
Jennifer A LiuDepartment of Neuroscience, Rockefeller Neuroscience Institute, West Virginia University, Morgantown, WV 26505, USA.
Paul D ChantlerDepartment of Neuroscience, Rockefeller Neuroscience Institute, West Virginia University, Morgantown, WV 26505, USA; Department of Human Performance and Exercise Physiology, West Virginia University, Morgantown, WV 26505, USA.
A Courtney DeVriesDepartment of Neuroscience, Rockefeller Neuroscience Institute, West Virginia University, Morgantown, WV 26505, USA; Department of Medicine, Division of Oncology/Hematology, West Virginia University, Morgantown, WV 26505, USA; West Virginia University Cancer Institute, West Virginia University, Morgantown, WV 26505, USA.
Randy J NelsonDepartment of Neuroscience, Rockefeller Neuroscience Institute, West Virginia University, Morgantown, WV 26505, USA.

Funding

Research Training Program in Behavioral and Biomedical SciencesT32GM132494 · NIGMS · WEST VIRGINIA UNIVERSITY · PI Anne Courtney DeVries, Kevin T Larkin · 2019 to 2026
$2.8M
Adverse Consequences of Light at Night for Cerebral IschemiaR01NS092388 · NINDS · WEST VIRGINIA UNIVERSITY · PI DEVRIES, ANNE COURTNEY, NELSON, RANDY J. · 2015 to 2019
$2.3M
NIGMS NIH HHS T32 GM132494NINDS NIH HHS R01 NS092388
6 · The paper itself

Abstract

Nearly every organism on Earth displays circadian organization of physiology and behavior, which is entrained to 24 h by daily exposure to bright light early during the day. However, the widespread presence of nocturnal electric lighting has blurred the boundary between day and night, leading to temporal desynchrony among individuals. Indeed, <6 weeks exposure to low levels of artificial light at night (ALAN) alters metabolism, energy, and sleep homeostasis in male mice. We hypothesized that ALAN would similarly affect female mice following prolonged exposure. After ≥20 weeks of exposure to dim ALAN, female mice had dampened locomotor rhythms, altered heat generation, respiratory exchange ratio (RER), and sleep. ALAN exposure decreased daily caloric intake, without altering body composition. The period and phase of the rhythm of sleep were significantly increased by ALAN, elevating the time spent sleeping during the active phase, without altering total sleep bout length. Taken together, these data indicate that ALAN impairs the rhythms in core physiological processes in female mice, but the mechanisms mediating these alterations may differ from those in males.

Indexed as

Circadian RhythmEnergy MetabolismLightLightingMotor ActivityPhotoperiodSleepAnimalsFemaleMaleMiceMice, Inbred C57BLArtificial light at nightCircadian rhythmsHeatLocomotor activityMetabolismRespiratory exchange ratioSleep

Identifiers

PMID42302962
PMCPMC13367374

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Registered trials

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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.