Evidence map›Paper›PMID 42539322›Full record

ArticlebioRxiv : the preprint server for biology2026

Circadian rhythm disruption alters rhythmic properties of clock and memory gene expression in the hippocampi of rats.

Scott H Deibel, Andrew B Lehr, Stavroula Michalopoulou, Incé Husain, Eugenio F Fornasiero, Cameron Bye, Nancy S Hong, Olga Kovalchuk, Robert J McDonald

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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

9 authors.

Scott H DeibelCanadian Centre for Behavioural Neuroscience, Department of Neuroscience, University of Lethbridge, Lethbridge, Alberta, Canada.
Andrew B LehrDepartment of Neuro- and Sensory Physiology, University Medical Center Göttingen, Göttingen, Germany.ORCID 0000-0002-1838-1847
Stavroula MichalopoulouDepartment of Neuro- and Sensory Physiology, University Medical Center Göttingen, Göttingen, Germany.
Incé HusainUniversity of New Brunswick, Department of Psychology, Fredericton, New Brunswick, Canada.
Eugenio F FornasieroDepartment of Neuro- and Sensory Physiology, University Medical Center Göttingen, Göttingen, Germany.ORCID 0000-0001-7643-4962
Cameron ByeCanadian Centre for Behavioural Neuroscience, Department of Neuroscience, University of Lethbridge, Lethbridge, Alberta, Canada.
Nancy S HongCanadian Centre for Behavioural Neuroscience, Department of Neuroscience, University of Lethbridge, Lethbridge, Alberta, Canada.
Olga KovalchukCanadian Centre for Behavioural Neuroscience, Department of Neuroscience, University of Lethbridge, Lethbridge, Alberta, Canada.
Robert J McDonaldCanadian Centre for Behavioural Neuroscience, Department of Neuroscience, University of Lethbridge, Lethbridge, Alberta, Canada.

Funding

Understanding protein turnover alterations in physiological brain agingR21AG085062 · NIA · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI FORNASIERO, EUGENIO FRANCESCO, JOVANOVIC, MARKO · 2024 to 2024
$413k
NIA NIH HHS R21 AG085062
6 · The paper itself

Abstract

Our modern environment - with its artificial lighting, irregular work hours, and frequent travel - often disrupts our circadian rhythms, which can lead to health problems, particularly in learning and memory. This is especially concerning given the aging population and the rising prevalence of dementia. Yet, the biological mechanisms linking circadian disruption to cognitive impairment remain poorly understood. At the molecular level, genetic techniques have been used to attenuate or abolish expression of key genes involved in circadian rhythms and these manipulations have detrimental effects on memory function. However, whether environmentally induced circadian disruption, impairs memory via changes in overall gene expression levels in the hippocampus or rather via changes in the coordinated rhythmic patterns of circadian expression across groups of genes is less known. Here, we examined how environmental circadian disruption affects the expression of genes involved in the circadian clock and memory in the hippocampus of rats using a forced desynchrony model. Circadian disruption changed the rhythmic properties of gene expression in most genes assessed but had no measurable effect on average expression levels across the day. These findings suggest that the inability to maintain circadian synchrony rather than overall expression may underlie the cognitive deficits observed in circadian-related disorders.

Indexed as

Circadian rhythm disruptionforced desynchronygene expressionhealthmemoryrats

Identifiers

PMID42539322
PMCPMC13419804

What OpenQuestion holds

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LicenceCC BY-ND
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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.