Evidence map›Paper›PMID 35363257›Full record

ArticleThe Journal of experimental medicine2022

Intermittent prednisone treatment in mice promotes exercise tolerance in obesity through adiponectin.

Mattia Quattrocelli, Michelle Wintzinger, Karen Miz, Manoj Panta, Ashok D Prabakaran, Grant D Barish, Navdeep S Chandel, Elizabeth M McNally

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

17 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
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  6. Adipokines: masterminds of metabolic inflammation.Nature reviews. Immunology · 2025
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  7. Hydroethanolic Extract ofTheScientificWorldJournal · 2025
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  11. Genome-Wide Association Analysis Identifies LILRB2 Gene for Pathological Myopia.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  12. Article
  13. Article
  14. Review
  15. A fat- and sucrose-enriched diet causes metabolic alterations in mdx mice.American journal of physiology. Regulatory, integrative and comparative physiology · 2023
    Article
  16. Article
  17. 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

8 authors at 2 institutions in 1 country.

Mattia QuattrocelliDivision of Molecular Cardiovascular Biology, Heart Institute, Cincinnati Children's Hospital Medical Center, and Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.ORCID 0000-0001-7011-1740
Michelle WintzingerDivision of Molecular Cardiovascular Biology, Heart Institute, Cincinnati Children's Hospital Medical Center, and Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.ORCID 0000-0001-7407-2048
Karen MizDivision of Molecular Cardiovascular Biology, Heart Institute, Cincinnati Children's Hospital Medical Center, and Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.ORCID 0000-0003-2498-502X
Manoj PantaDivision of Molecular Cardiovascular Biology, Heart Institute, Cincinnati Children's Hospital Medical Center, and Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.ORCID 0000-0002-4168-3202
Ashok D PrabakaranDivision of Molecular Cardiovascular Biology, Heart Institute, Cincinnati Children's Hospital Medical Center, and Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.ORCID 0000-0001-9053-2673
Grant D BarishDivision of Endocrinology, Metabolism and Molecular Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL.ORCID 0000-0001-8753-0546
Navdeep S ChandelDepartment of Medicine and Department of Biochemistry and Molecular Genetics, Northwestern University Feinberg School of Medicine, Chicago, IL.ORCID 0000-0001-7208-3886
Elizabeth M McNallyCenter for Genetic Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL.ORCID 0000-0002-1221-719X
Cincinnati Children's Hospital Medical Center · USNorthwestern University · US

Funding

Tissue resident macrophages regulate proteostasis in the aging lungP01AG049665 · NIA · NORTHWESTERN UNIVERSITY AT CHICAGO · PI GR Scott Budinger · 2015 to 2026
$26.9M
Training and education CoreU54AR052646 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI MCNALLY, ELIZABETH M, SWEENEY, H LEE · 2005 to 2020
$24.1M
SARCOGLYCAN IN MYOPATHY AND MUSCLE MEMBRANE STABILITYR01HL061322 · NHLBI · UNIVERSITY OF CHICAGO · PI MCNALLY, ELIZABETH M · 1999 to 2022
$7.5M
Myoferlin in Muscle Membrane Fusion and RepairR01NS047726 · NINDS · UNIVERSITY OF CHICAGO · PI ALEXIS R. DEMONBREUN, Elizabeth M McNally · 2003 to 2026
$7.2M
Understanding and Improving Therapies for the Muscular Dystrophies through Noninvasive BiomarkersP50AR052646 · NIAMS · UNIVERSITY OF FLORIDA · PI SWEENEY, H LEE · 2021 to 2024
$6.2M
Nuclear Repressors in Genomic Control of Healthful ObesityR01DK108987 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI BARISH, GRANT D · 2016 to 2024
$3.4M
Integrative Genomics, Epigenomics and Bioinformatics Analyses of Human Uterine FibroidsR01HD089552 · NICHD · NORTHWESTERN UNIVERSITY AT CHICAGO · PI BARISH, GRANT D, BULUN, SERDAR E. · 2016 to 2020
$3.4M
Coordinated mechanisms to rescue bioenergetics and sarcopenia in agingR01AG078174 · NIA · CINCINNATI CHILDRENS HOSP MED CTR · PI QUATTROCELLI, MATTIA · 2022 to 2025
$1.3M
Glucocorticoid and circadian clock coregulation of insulin sensitivity and metabolismK01DK121875 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI QUATTROCELLI, MATTIA · 2019 to 2021
$444k
CHRONO-MECHANISMS of CARDIOMETABOLIC PHARMACOLOGYR56HL158531 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI QUATTROCELLI, MATTIA · 2021 to 2021
$398k
BLRD VA I01 BX004898NHLBI NIH HHS R01 HL061322NHLBI NIH HHS R56 HL158531NIAMS NIH HHS P50 AR052646NIAMS NIH HHS U54 AR052646NIA NIH HHS P01 AG049665NIA NIH HHS R01 AG078174NICHD NIH HHS R01 HD089552NIDDK NIH HHS K01 DK121875NIDDK NIH HHS R01 DK108987NINDS NIH HHS R01 NS047726
6 · The paper itself

Abstract

The fat-muscle communication regulates metabolism and involves circulating signals like adiponectin. Modulation of this cross-talk could benefit muscle bioenergetics and exercise tolerance in conditions like obesity. Chronic daily intake of exogenous glucocorticoids produces or exacerbates metabolic stress, often leading to obesity. In stark contrast to the daily intake, we discovered that intermittent pulses of glucocorticoids improve dystrophic muscle metabolism. However, the underlying mechanisms, particularly in the context of obesity, are still largely unknown. Here we report that in mice with diet-induced obesity, intermittent once-weekly prednisone increased total and high-molecular weight adiponectin levels and improved exercise tolerance and energy expenditure. These effects were dependent upon adiponectin, as shown by genetic ablation of the adipokine. Upregulation of Adipoq occurred through the glucocorticoid receptor (GR), as this effect was blocked by inducible GR ablation in adipocytes. The treatment increased the muscle metabolic response of adiponectin through the CAMKK2-AMPK cascade. Our study demonstrates that intermittent glucocorticoids produce healthful metabolic remodeling in diet-induced obesity.

Indexed as

AdiponectinExercise ToleranceAdipocytesAnimalsMiceObesityPrednisoneAdiponectinPrednisone

Identifiers

PMID35363257
PMCPMC8980841
OpenAlexW4224017544

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.