Evidence map›Paper›PMID 42550878›Full record

ArticlePLoS biology2026

Meal timing entrains circadian rhythms in the dorsal vagal complex, a brainstem satiety centre.

Lukasz Chrobok, Charlotte Muir, Tanya Chonkria Kaur, Emily Birt, Iliana Veneri, Jingyi Kathy Li, Timna Hitrec, Michael Ambler, Anthony Edward Pickering, Hugh David Piggins

Abstract read
In one paragraph

Article in PLoS 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

10 authors.

Lukasz ChrobokSchool of Physiology, Pharmacology, and Neuroscience, Faculty of Life Sciences, University of Bristol, Bristol, United Kingdom.ORCID https://orcid.org/0000-0002-0118-2833
Charlotte MuirSchool of Physiology, Pharmacology, and Neuroscience, Faculty of Life Sciences, University of Bristol, Bristol, United Kingdom.
Tanya Chonkria KaurSchool of Physiology, Pharmacology, and Neuroscience, Faculty of Life Sciences, University of Bristol, Bristol, United Kingdom.
Emily BirtSchool of Physiology, Pharmacology, and Neuroscience, Faculty of Life Sciences, University of Bristol, Bristol, United Kingdom.
Iliana VeneriSchool of Physiology, Pharmacology, and Neuroscience, Faculty of Life Sciences, University of Bristol, Bristol, United Kingdom.
Jingyi Kathy LiSchool of Physiology, Pharmacology, and Neuroscience, Faculty of Life Sciences, University of Bristol, Bristol, United Kingdom.
Timna HitrecSchool of Physiology, Pharmacology, and Neuroscience, Faculty of Life Sciences, University of Bristol, Bristol, United Kingdom.
Michael AmblerSchool of Physiology, Pharmacology, and Neuroscience, Faculty of Life Sciences, University of Bristol, Bristol, United Kingdom.
Anthony Edward PickeringSchool of Physiology, Pharmacology, and Neuroscience, Faculty of Life Sciences, University of Bristol, Bristol, United Kingdom.
Hugh David PigginsSchool of Physiology, Pharmacology, and Neuroscience, Faculty of Life Sciences, University of Bristol, Bristol, United Kingdom.

Funding

Wellcome Trust
6 · The paper itself

Abstract

The dorsal vagal complex (DVC) includes a multi-component brainstem satiety centre which has gained attention as a key target of anti-obesity pharmacotherapies. Our recent studies revealed its circadian timekeeping properties, with molecular and electrophysiological 24 h rhythms persisting independently of the primary hypothalamic clock. However, the factors entraining these brainstem oscillators and the downstream transcriptional targets of the DVC molecular clock remain unclear. Here, using PERIOD2::LUCIFERASE reporter mice and fluorescent in situ hybridisation, we quantitatively demonstrate rhythms in core clock gene expression in the caudal DVC ex vivo and in vivo. We show that the molecular clock is associated with rhythmic expression of numerous neurotransmitter receptor genes in the DVC in vivo, with the phase of both clock and clock-controlled gene expression tightly regulated by meal timing. These findings uncover food-entrained circadian rhythms in the DVC and have important implications for clinical studies targeting brainstem satiety mechanisms.

Indexed as

Brain StemCircadian RhythmFeeding BehaviorMealsSatiety ResponseVagus NerveAnimalsGene Expression RegulationMaleMiceMice, Inbred C57BLMice, TransgenicPeriod Circadian ProteinsPer2 protein, mousePeriod Circadian Proteins

Identifiers

PMID42550878
PMCPMC13460586

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LicenceCC BY
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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.