Evidence map›Paper›PMID 39796454›Full record

ArticleNutrients2024

Urolithin A Modulates PER2 Degradation via SIRT1 and Enhances the Amplitude of Circadian Clocks in Human Senescent Cells.

Rassul Kuatov, Jiro Takano, Hideyuki Arie, Masaru Kominami, Norifumi Tateishi, Ken-Ichi Wakabayashi, Daisuke Takemoto, Takayuki Izumo, Yoshihiro Nakao, Wataru Nakamura and 2 more

Abstract read
In one paragraph

Article in Nutrients, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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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

12 authors.

Rassul KuatovDepartment of Neurobiology & Behavior, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki 852-8523, Japan.
Jiro TakanoInstitute for Science of Life, Suntory Wellness Limited, Kyoto 619-0284, Japan.
Hideyuki ArieInstitute for Science of Life, Suntory Wellness Limited, Kyoto 619-0284, Japan.ORCID 0000-0001-9166-9831
Masaru KominamiInstitute for Science of Life, Suntory Wellness Limited, Kyoto 619-0284, Japan.
Norifumi TateishiInstitute for Science of Life, Suntory Wellness Limited, Kyoto 619-0284, Japan.
Ken-Ichi WakabayashiInstitute for Science of Life, Suntory Wellness Limited, Kyoto 619-0284, Japan.
Daisuke TakemotoInstitute for Science of Life, Suntory Wellness Limited, Kyoto 619-0284, Japan.ORCID 0000-0003-3465-0581
Takayuki IzumoInstitute for Science of Life, Suntory Wellness Limited, Kyoto 619-0284, Japan.
Yoshihiro NakaoInstitute for Science of Life, Suntory Wellness Limited, Kyoto 619-0284, Japan.
Wataru NakamuraDepartment of Oral-Chrono Physiology, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki 852-8588, Japan.
Kazuyuki ShinoharaDepartment of Neurobiology & Behavior, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki 852-8523, Japan.
Yasukazu NakahataDepartment of Neurobiology & Behavior, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki 852-8523, Japan.ORCID 0000-0003-3814-5822

Funding

JSPS KAKENHI 22K06320Suntory Wellness Limited
6 · The paper itself

Abstract

BACKGROUND/

objectivesCircadian clocks are endogenous systems that regulate numerous biological, physiological, and behavioral events in living organisms. Aging attenuates the precision and robustness of circadian clocks, leading to prolonged and dampened circadian gene oscillation rhythms and amplitudes. This study investigated the effects of food-derived polyphenols such as ellagic acid and its metabolites (urolithin A, B, and C) on the aging clock at the cellular level using senescent human fibroblast cells, TIG-3 cells.

methodsLentivirus-infected TIG-3 cells expressing Bmal1-luciferase were used for real-time luciferase monitoring assays.

resultsWe revealed that urolithins boosted the amplitude of circadian gene oscillations at different potentials; urolithin A (UA) amplified the best. Furthermore, we discovered that UA unstabilizes PER2 protein while stabilizing SIRT1 protein, which provably enhances

conclusionsThe findings suggest that urolithins, particularly UA, have the potential to modulate the aging clock and may serve as therapeutic nutraceuticals for age-related disorders associated with circadian dysfunction.

Indexed as

Cellular SenescenceCircadian ClocksCoumarinsPeriod Circadian ProteinsSirtuin 1ARNTL Transcription FactorsCell LineCircadian RhythmFibroblastsHumans3,8-dihydroxy-6H-dibenzo(b,d)pyran-6-oneARNTL Transcription FactorsBMAL1 protein, humanCoumarinsPER2 protein, humanPeriod Circadian ProteinsSIRT1 protein, humanSirtuin 1antiagingcircadian clockellagic acidsenescent cellsurolithin A

Identifiers

PMID39796454
PMCPMC11722880

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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.