Evidence mapPaperPMID 41511549Full record

ArticleCellular and molecular life sciences : CMLS2026

Modeling the dynamics of hepatic metabolism: the predominance of 12-hour rhythmicity in metabolic adaptation.

Madlen Matz-Soja, Christiane Körner, Fritzi Ott, Janett Fischer, Eugenia Marbach-Breitrück, Christian Bergmann, Ute Hofmann, Andrej Shevchenko, Iwona Wallach, Kathrin Textoris-Taube and 4 more

Abstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

14 authors.

Madlen Matz-Soja *Division of Hepatology, Department of Medicine II, Laboratory for Clinical and Experimental Hepatology, Leipzig University Medical Center, Leipzig, Germany.
Christiane Körner *Division of Hepatology, Department of Medicine II, Laboratory for Clinical and Experimental Hepatology, Leipzig University Medical Center, Leipzig, Germany.
Fritzi OttDivision of Hepatology, Department of Medicine II, Laboratory for Clinical and Experimental Hepatology, Leipzig University Medical Center, Leipzig, Germany.
Janett FischerDivision of Hepatology, Department of Medicine II, Laboratory for Clinical and Experimental Hepatology, Leipzig University Medical Center, Leipzig, Germany.
Eugenia Marbach-BreitrückRudolf-Schönheimer-Institute of Biochemistry, Faculty of Medicine, Leipzig University, Leipzig, Germany.
Christian BergmannDivision of Hepatology, Department of Medicine II, Laboratory for Clinical and Experimental Hepatology, Leipzig University Medical Center, Leipzig, Germany.
Ute HofmannDr. Margarete Fischer‑Bosch Institute of Clinical Pharmacology, University of Tübingen, Stuttgart, Germany.
Andrej ShevchenkoMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Iwona WallachDepartment of Radiology, , Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.
Kathrin Textoris-TaubeCore Facility High Throughput Mass Spectrometry, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.
Michael MüllederCore Facility High Throughput Mass Spectrometry, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.
Rolf GebhardtRudolf-Schönheimer-Institute of Biochemistry, Faculty of Medicine, Leipzig University, Leipzig, Germany.
Thomas BergDivision of Hepatology, Department of Medicine II, Laboratory for Clinical and Experimental Hepatology, Leipzig University Medical Center, Leipzig, Germany.
Nikolaus BerndtDepartment of Radiology, , Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany. nikolaus.berndt@dife.de.ORCID http://orcid.org/0000-0001-5594-9940

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesThe liver continuously adjusts its metabolic activity to synchronize the nutrient supply with the body's demands. This synchronization involves the complex coordination of acute metabolic needs, nutrient availability, and activity levels, which is orchestrated according to cyclic internal rhythms governed by the circadian clock. This study aimed to decipher the role of circadian rhythms in liver metabolic functions, including mitochondrial activities that are critical for energy production and metabolic adaptation.

methodsWe investigated rhythmic changes in liver metabolism via comprehensive multiomics and kinetic mathematical modeling. The liver proteome of male mice was analyzed and modeled, and complementary serum lipidomic and metabolomic analyses were performed. Mitochondrial proteins were examined to evaluate the role of mitochondria in the oscillating regulation of energy production.

resultsMost metabolic functions, particularly those related to carbohydrate and fatty acid metabolism, exhibit rhythmic patterns on a 12-hour rather than a 24-hour cycle. The importance of this rhythmicity is function-dependent and can account for 25% to 50% of the overall variability. Mitochondrial activities also exhibit temporal fluctuations that are closely linked to nutrient availability. The strong correlation between metabolic functions and serum metabolites highlights the precise alignment between physiological demand and metabolic performance.

conclusionsHepatic metabolic functions follow a 12-hour cycle rather than a 24-hour cycle, significantly contributing to the liver's ability to meet nutrient demands throughout the day. Mitochondrial dynamics, which are influenced by nutrient availability, play a central role in adapting energy production to the body's metabolic needs.

Indexed as

Adaptation, PhysiologicalCircadian RhythmLiverModels, BiologicalAnimalsEnergy MetabolismFatty AcidsMaleMiceMice, Inbred C57BLMitochondriaMultiomicsProteomeFatty AcidsProteomeCircadian/diurnal rhythmHEPATOKIN1Kinetic modelingLiverMetabolismMitochondriaMultiomics

Identifiers

PMID41511549
PMCPMC12819941

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 Socratic graph.