Evidence map›Paper›PMID 41987529›Full record

ArticleJournal of cellular physiology2026

Clock Modulation by Naringenin Suppresses Lipogenesis and Promotes Adipose Tissue Browning.

Xuekai Xiong, Jemima Pangemanan, Tali Kiperman, Zuoming Sun, Antoni Paul, Vijay Yechoor, Ke Ma

Abstract read
In one paragraph

Article in Journal of cellular physiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Xuekai XiongDepartment of Diabetes Complications and Metabolism, Beckman Research Institute of City of Hope, Duarte, California, USA.
Jemima PangemananDepartment of Diabetes Complications and Metabolism, Beckman Research Institute of City of Hope, Duarte, California, USA.
Tali KipermanDepartment of Diabetes Complications and Metabolism, Beckman Research Institute of City of Hope, Duarte, California, USA.
Zuoming SunDepartment of Molecular Imaging and Therapy, Beckman Research Institute of City of Hope, Duarte, California, USA.ORCID https://orcid.org/0000-0003-1896-6666
Antoni PaulDepartment of Molecular and Cellular Physiology, Albany Medical College, Albany, New York, USA.
Vijay YechoorDivision of Endocrinology and Metabolism, Diabetes and Beta Cell Biology Center, Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Ke MaDepartment of Diabetes Complications and Metabolism, Beckman Research Institute of City of Hope, Duarte, California, USA.ORCID https://orcid.org/0000-0002-5206-1038

Funding

Clock modulation in circadian desynchrony induced diabetes and atherovascular disease - mechanisms and interventionsR01DK128972 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI FIGUEIRO, MARIANA GROSS, PAUL, ANTONIO · 2021 to 2025
$3.7M
Circadian clock and temporal control in nutrient metabolismR01DK137515 · NIDDK · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI Ke Ma · 2023 to 2026
$1.8M
Circadian Clock Control of Adipose Depot Development and FunctionR01DK112794 · NIDDK · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI MA, KE · 2018 to 2021
$1.7M
Circadian Clock and Beta Cell Stress AdaptationR01DK097160 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI YECHOOR, VIJAY K · 2014 to 2018
$1.7M
Circadian clock regulation of metabolic pathways in agingR56AG080294 · NIA · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI MA, KE · 2023 to 2023
$440k
NIA NIH HHS R56 AG080294NIA NIH HHS R56AG080294NIDDK NIH HHS R01DK097160NIDDK NIH HHS R01DK112794NIDDK NIH HHS R01DK128972NIDDK NIH HHS R01 DK137515
6 · The paper itself

Abstract

The circadian clock orchestrates adipocyte development and lipid remodeling, with its disruption leading to the development of obesity and insulin resistance. Here we demonstrate that the flavonoid compound naringenin displays clock modulatory activity that suppresses adipocyte lipid storage while promoting browning. In adipogenic progenitors, naringenin activates RORα with induction of clock gene expression to promote circadian clock oscillation with protective effect against cytokine-induced dampening. The clock-enhancing properties of naringenin suppressed lipogenesis in mature adipocytes together with induction of browning characteristics. The inhibitory effect of naringenin on lipogenesis was dependent on clock modulation as it was abolished in RORα-deficient adipocytes. We further show that naringenin administration in vivo up-regulated RORα expression with clock gene induction together with browning of subcutaneous beige fat depot, resulting reduced fat mass and body weight. Naringenin treatment in vivo also lowered plasma glucose and free fatty acid levels, with markedly enhanced insulin signaling in adipose depots and skeletal muscle. Collectively, our findings uncover a new clock-activating mechanism of action in mediating the metabolic benefits of naringenin, suggesting its potential as a natural supplement for anti-obesity and metabolic disease interventions.

Indexed as

Adipose Tissue, BrownCircadian ClocksCLOCK ProteinsFlavanonesLipogenesis3T3-L1 CellsAdipocytesAdipogenesisAnimalsInsulinMaleMiceMice, Inbred C57BLNuclear Receptor Subfamily 1, Group F, Member 1Signal TransductionClock protein, mouseCLOCK ProteinsFlavanonesInsulinnaringeninNuclear Receptor Subfamily 1, Group F, Member 1beige adipocyteCircadian clockflavonoidslipogenesisobesityRORα

Identifiers

PMID41987529
PMCPMC13084208

What OpenQuestion holds

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LicenceCC BY-NC-ND
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 OpenQuestion graph.