Evidence map›Paper›PMID 40580317›Full record

ArticleCellular and molecular life sciences : CMLS2025

Circadian ontogenetic metabolomics atlas: an interactive resource with insights from rat plasma, tissues, and feces.

Lucie Rudl Kulhava, Pavel Houdek, Michaela Novakova, Jiri Hricko, Michaela Paucova, Ondrej Kuda, Martin Sladek, Oliver Fiehn, Alena Sumova, Tomas Cajka

Abstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2025. 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

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

2 citing papers in PubMed.

  1. Article
  2. Article
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.

Lucie Rudl Kulhava *Institute of Physiology of the Czech Academy of Sciences, Videnska 1083, Prague, 14200, Czech Republic.
Pavel Houdek *Institute of Physiology of the Czech Academy of Sciences, Videnska 1083, Prague, 14200, Czech Republic.
Michaela Novakova *Institute of Physiology of the Czech Academy of Sciences, Videnska 1083, Prague, 14200, Czech Republic.
Jiri HrickoInstitute of Physiology of the Czech Academy of Sciences, Videnska 1083, Prague, 14200, Czech Republic.
Michaela PaucovaInstitute of Physiology of the Czech Academy of Sciences, Videnska 1083, Prague, 14200, Czech Republic.
Ondrej KudaInstitute of Physiology of the Czech Academy of Sciences, Videnska 1083, Prague, 14200, Czech Republic.
Martin SladekInstitute of Physiology of the Czech Academy of Sciences, Videnska 1083, Prague, 14200, Czech Republic.
Oliver FiehnUniversity of California, Davis, 451 Health Sciences Drive, Davis, CA, 95616, USA.
Alena SumovaInstitute of Physiology of the Czech Academy of Sciences, Videnska 1083, Prague, 14200, Czech Republic. alena.sumova@fgu.cas.cz.
Tomas CajkaInstitute of Physiology of the Czech Academy of Sciences, Videnska 1083, Prague, 14200, Czech Republic. tomas.cajka@fgu.cas.cz.ORCID http://orcid.org/0000-0002-9728-3355

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Circadian rhythms regulate key physiological processes through clock genes in central and peripheral tissues. While circadian gene expression during development has been well studied, the temporal dynamics of metabolism across tissues remain less understood. Here, we present the Circadian Ontogenetic Metabolomics Atlas (COMA), which maps circadian metabolic rhythms across 16 rat anatomical structures. The brain (suprachiasmatic nuclei, medial prefrontal cortex) and periphery (liver, plasma) span developmental stages from embryonic E19 to postnatal P2, P10, P20, and P28. Fecal samples include all four postnatal stages, while additional peripheral tissues were analyzed at P20 and P28. Using a multiplatform liquid chromatography-mass spectrometry approach, we annotated 851 metabolites from 1610 samples. We identified distinct circadian shifts, particularly during the transition from nursing to solid food intake (P10-P20), with an average of 24% of metabolites exhibiting circadian oscillations across sample types, as determined by JTK_CYCLE. Our study also underscores the importance of standardized sampling, as metabolite intensities fluctuate with both circadian rhythms and development. COMA serves as an open-access resource ( https://coma.metabolomics.fgu.cas.cz ) for exploring circadian metabolic regulation and its role in developmental biology.

Indexed as

Circadian RhythmFecesMetabolomeMetabolomicsAnimalsChromatography, LiquidFemaleLiverMaleRatsAtlasCircadian rhythmLipidomicsMetabolomicsResource

Identifiers

PMID40580317
PMCPMC12206216

What Socratic holds

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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 Socratic graph.