Evidence map›Paper›PMID 35767959›Full record

ArticleCell reports2022

Flattening of circadian glucocorticoid oscillations drives acute hyperinsulinemia and adipocyte hypertrophy.

Stefan Tholen, Roma Patel, Agnieszka Agas, Kyle M Kovary, Atefeh Rabiee, Hayley T Nicholls, Ewa Bielczyk-Maczyńska, Wenting Yang, Fredric B Kraemer, Mary N Teruel

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.7field-weighted citation impact, top 16% of its field
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

9 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Circadian clock communication during homeostasis and ageing.Nature reviews. Molecular cell biology · 2025
    Review
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  7. Article
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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

10 authors at 3 institutions in 1 country.

Stefan TholenDepartment of Chemical and Systems Biology, Stanford University, Stanford, CA 94305, USA.
Roma PatelDepartment of Biochemistry and the Gale and Ira Drukier Institute of Children's Health, Weill Cornell Medical College of Cornell University, New York, NY, USA.
Agnieszka AgasDepartment of Biochemistry and the Gale and Ira Drukier Institute of Children's Health, Weill Cornell Medical College of Cornell University, New York, NY, USA.
Kyle M KovaryDepartment of Chemical and Systems Biology, Stanford University, Stanford, CA 94305, USA.
Atefeh RabieeDepartment of Chemical and Systems Biology, Stanford University, Stanford, CA 94305, USA.
Hayley T NichollsWeill Center for Metabolic Health, Division of Endocrinology, Diabetes and Metabolism, Joan and Sanford I. Weill Department of Medicine, Weill Cornell Medical College of Cornell University, New York, NY, USA.
Ewa Bielczyk-MaczyńskaDepartment of Chemical and Systems Biology, Stanford University, Stanford, CA 94305, USA.
Wenting YangDepartment of Chemical and Systems Biology, Stanford University, Stanford, CA 94305, USA.
Fredric B KraemerDepartment of Medicine, Division of Endocrinology, Stanford University, Stanford, CA, USA; VA Palo Alto Health Care System, Palo Alto, CA 94305, USA.
Mary N TeruelDepartment of Chemical and Systems Biology, Stanford University, Stanford, CA 94305, USA; Department of Bioengineering, Stanford University, Stanford, CA 94305, USA; Department of Biochemistry and the Gale and Ira Drukier Institute of Children's Health, Weill Cornell Medical College of Cornell University, New York, NY, USA; Weill Center for Metabolic Health, Division of Endocrinology, Diabetes and Metabolism, Joan and Sanford I. Weill Department of Medicine, Weill Cornell Medical College of Cornell University, New York, NY, USA. Electronic address: mnt4002@med.cornell.edu.
Stanford University · USCornell University · USVA Palo Alto Health Care System · US

Funding

TRAINING & OUTREACH COREP50GM107615 · NIGMS · STANFORD UNIVERSITY · PI FERRELL, JAMES E. · 2013 to 2017
$10.9M
Them1-Mediated Metabolic Regulation and Pathogenic Role in NAFLDR01DK103046 · NIDDK · WEILL MEDICAL COLL OF CORNELL UNIV · PI DAVID E. COHEN, Susan J Hagen · 2015 to 2026
$7.6M
Cell cycle control of adipogenesisR01DK131432 · NIDDK · WEILL MEDICAL COLL OF CORNELL UNIV · PI Mary N Teruel · 2023 to 2026
$2.0M
Controlling tissue size by noise and feedbackR01DK106241 · NIDDK · WEILL MEDICAL COLL OF CORNELL UNIV · PI TERUEL, MARY N · 2015 to 2018
$1.4M
Controlling the rate of adipocyte differentiation: Experiments and theoryR01DK101743 · NIDDK · WEILL MEDICAL COLL OF CORNELL UNIV · PI TERUEL, MARY N · 2015 to 2017
$1.1M
Cell cycle control of adipogenesisR56DK131432 · NIDDK · WEILL MEDICAL COLL OF CORNELL UNIV · PI TERUEL, MARY N · 2021 to 2021
$211k
LipolysisI01BX000398 · VA · VETERANS ADMIN PALO ALTO HEALTH CARE SYS · PI KRAEMER, FREDRIC B. · 2009 to 2020
–
BLRD VA I01 BX000398NIDDK NIH HHS R01 DK101743NIDDK NIH HHS R01 DK103046NIDDK NIH HHS R01 DK106241NIDDK NIH HHS R01 DK131432NIDDK NIH HHS R56 DK131432NIGMS NIH HHS P50 GM107615
6 · The paper itself

Abstract

Disruption of circadian glucocorticoid oscillations in Cushing's disease and chronic stress results in obesity and adipocyte hypertrophy, which is believed to be a main source of the harmful effects of obesity. Here, we recapitulate stress due to jet lag or work-life imbalances by flattening glucocorticoid oscillations in mice. Within 3 days, mice achieve a metabolic state with persistently high insulin, but surprisingly low glucose and fatty acids in the bloodstream, that precedes a more than 2-fold increase in brown and white adipose tissue mass within 3 weeks. Transcriptomic and Cd36-knockout mouse analyses show that hyperinsulinemia-mediated de novo fatty acid synthesis and Cd36-mediated fatty acid uptake drive fat mass increases. Intriguingly, this mechanism by which glucocorticoid flattening causes acute hyperinsulinemia and adipocyte hypertrophy is unexpectedly beneficial in preventing high levels of circulating fatty acids and glucose for weeks, thus serving as a protective response to preserve metabolic health during chronic stress.

Indexed as

GlucocorticoidsHyperinsulinismAdipocytesAnimalsFatty AcidsGlucoseHypertrophyMiceObesityFatty AcidsGlucocorticoidsGlucosebrown adipose tissueCd36circadian rhythmCP: Metabolismglucocorticoidshormone oscillationslipid metabolismobesitystresswhite adipose tissue

Identifiers

PMID35767959
PMCPMC9391061
OpenAlexW4283711466

What OpenQuestion holds

Textmetadata
LicenceTDM
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.