Evidence map›Paper›PMID 31206703›Full record

ArticleThe Journal of physiology2019

Anti-inflammatory effects of oestrogen mediate the sexual dimorphic response to lipid-induced insulin resistance.

João Paulo Camporez, Kun Lyu, Emily L Goldberg, Dongyan Zhang, Gary W Cline, Michael J Jurczak, Vishwa Deep Dixit, Kitt Falk Petersen, Gerald I Shulman

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of physiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

55 citing papers in PubMed, 66 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Insulin receptorNature communications · 2026
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Growth hormone receptor in VGLUT2 or Sim1 cells regulates glycemia and insulin sensitivity.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  13. Article
  14. Article
  15. Sex-Dependent T Cell Dysregulation in Mice with Diet-Induced Obesity.International journal of molecular sciences · 2024
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. The Metabolic Syndrome, a Human Disease.International journal of molecular sciences · 2024
    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

9 authors at 4 institutions in 3 countries.

João Paulo CamporezDepartment of Internal Medicine, Yale University School of Medicine, New Haven, CT, 06520, USA.ORCID 0000-0003-3486-4301
Kun LyuDepartment of Internal Medicine, Yale University School of Medicine, New Haven, CT, 06520, USA.
Emily L GoldbergComparative Medicine, Yale University School of Medicine, New Haven, CT, 06520, USA.
Dongyan ZhangDepartment of Internal Medicine, Yale University School of Medicine, New Haven, CT, 06520, USA.
Gary W ClineDepartment of Internal Medicine, Yale University School of Medicine, New Haven, CT, 06520, USA.
Michael J JurczakDepartment of Medicine, University of Pittsburgh, Pittsburgh, PA, 15261, USA.
Vishwa Deep DixitComparative Medicine, Yale University School of Medicine, New Haven, CT, 06520, USA.
Kitt Falk PetersenDepartment of Internal Medicine, Yale University School of Medicine, New Haven, CT, 06520, USA.
Gerald I ShulmanDepartment of Internal Medicine, Yale University School of Medicine, New Haven, CT, 06520, USA.
Yale University · USHoward Hughes Medical Institute · USUniversidade de São Paulo · BRUniversity of Pittsburgh · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Yale Diabetes Research CenterP30DK045735 · NIDDK · YALE UNIVERSITY · PI Kevan C Herold, GERALD I SHULMAN · 1993 to 2026
$44.0M
The role of AgRP/Auga-ALK pathway in FGF21's brain action on agingP01AG051459 · NIA · YALE UNIVERSITY · PI VISHWA DEEP DIXIT · 2016 to 2026
$25.7M
Mechanism of Insulin Resistance in the Aged.R01AG023686 · NIA · YALE UNIVERSITY · PI PETERSEN, KITT F · 2003 to 2014
$3.4M
Thymic adipogenesis and age-related thymic demiseR01AI105097 · NIAID · YALE UNIVERSITY · PI DIXIT, VISHWA DEEP · 2015 to 2018
$1.9M
Impact of Ketone Metabolites on Inflammasome Deactivation in GoutR01AR070811 · NIAMS · YALE UNIVERSITY · PI DIXIT, VISHWA DEEP · 2017 to 2021
$1.8M
Inflammasomes and the mechanism of thymic demise in agingR01AG043608 · NIA · YALE UNIVERSITY · PI DIXIT, VISHWA DEEP · 2013 to 2017
$1.8M
Glucagon Regulation of Hepatic Mitochondrial Activity and Glucose Metabolism by InsP3R-1R01DK116774 · NIDDK · YALE UNIVERSITY · PI SHULMAN, GERALD I · 2018 to 2021
$1.7M
Parkin's role in hepatic mitochondrial turnover, steatosis and insulin resistanceK01DK099402 · NIDDK · YALE UNIVERSITY · PI JURCZAK, MICHAEL J. · 2013 to 2015
$441k
Thymic adipogenesis and age-related thymic demiseR56AI105097 · NIAID · YALE UNIVERSITY · PI DIXIT, VISHWA DEEP · 2013 to 2013
$348k
Impact of ketone bodies on age-related inflammation and healthspan extensionK99AG058801 · NIA · YALE UNIVERSITY · PI GOLDBERG, EMILY LAUREN · 2019 to 2020
$203k
NCATS NIH HHS UL1 TR001863NIAID NIH HHS R01 AI105097NIAID NIH HHS R56 AI105097NIAMS NIH HHS R01 AR070811NIA NIH HHS K99 AG058801NIA NIH HHS P01 AG051459NIA NIH HHS R01 AG023686NIA NIH HHS R01 AG043608NIDDK NIH HHS K01 DK099402NIDDK NIH HHS P30 DK045735NIDDK NIH HHS R01 DK116774
6 · The paper itself

Abstract

key pointsOestrogen has been shown to play an important role in the regulation of metabolic homeostasis and insulin sensitivity in both human and rodent studies. Insulin sensitivity is greater in premenopausal women compared with age-matched men, and metabolism-related cardiovascular diseases and type 2 diabetes are less frequent in these same women. Both female and male mice treated with oestradiol are protected against obesity-induced insulin resistance. The protection against obesity-induced insulin resistance is associated with reduced ectopic lipid content in liver and skeletal muscle. These results were associated with increased insulin-stimulated suppression of white adipose tissue lipolysis and reduced inflammation. ABSTRACT: Oestrogen has been shown to play an important role in the regulation of metabolic homeostasis and insulin sensitivity in both human and rodent studies. Overall, females are protected against obesity-induced insulin resistance; yet, the mechanisms responsible for this protection are not well understood. Therefore, the aim of the present work was to evaluate the underlying mechanism(s) by which female mice are protected against obesity-induced insulin resistance compared with male mice. We studied male and female mice in age-matched or body weight-matched conditions. They were fed a high-fat diet (HFD) or regular chow for 4 weeks. We also studied HFD male mice treated with oestradiol or vehicle. Both HFD female and HFD male mice treated with oestradiol displayed increased whole-body insulin sensitivity, associated with reduction in ectopic hepatic and muscle lipid content compared to HFD male mice. Reductions in ectopic lipid content in these mice were associated with increased insulin-stimulated suppression of white adipose tissue (WAT) lipolysis. Both HFD female and HFD male mice treated with oestradiol also displayed striking reductions in WAT inflammation, represented by reductions in plasma and adipose tissue tumour necrosis factor α and interleukin 6 concentrations. Taken together these data support the hypothesis that HFD female mice are protected from obesity-induced insulin resistance due to oestradiol-mediated reductions in WAT inflammation, leading to improved insulin-mediated suppression of WAT lipolysis and reduced ectopic lipid content in liver and skeletal muscle.

Indexed as

Insulin ResistanceSex CharacteristicsAdipose Tissue, WhiteAnimalsBody WeightCell LineCells, CulturedDiet, High-FatEstrogensFemaleInterleukin-6LipolysisLiverMaleMiceMice, Inbred C57BLEstrogensInterleukin-6Tumor Necrosis Factor-alphaEstradiolInsulin resistanceNAFLDSexual dimorphism

Identifiers

PMID31206703
PMCPMC6876753
OpenAlexW2953132933

What OpenQuestion holds

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Registered trials

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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.