Evidence map›Paper›PMID 30087356›Full record

ArticleScientific reports2018

An orally-active adiponectin receptor agonist mitigates cutaneous fibrosis, inflammation and microvascular pathology in a murine model of systemic sclerosis.

Takashi Yamashita, Katja Lakota, Takashi Taniguchi, Ayumi Yoshizaki, Shinichi Sato, Wen Hong, Xingchun Zhou, Snezn Sodin-Semrl, Feng Fang, Yoshihide Asano and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
4.7field-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

33 citing papers in PubMed, 53 citations in OpenAlex.

  1. Trial
  2. Review
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  5. Review
  6. Immunopharmacological potential ofFrontiers in pharmacology · 2025
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Plant miR167e-5p promotes 3T3-L1 adipocyte adipogenesis by targeting β-catenin.In vitro cellular & developmental biology. Animal · 2022
    Article
  16. Article
  17. The Role of Adiponectin in the Skin.Biomolecules & therapeutics · 2022
    Review
  18. Review
  19. Review
  20. Endothelial-to-mesenchymal transition in systemic sclerosis.Clinical and experimental immunology · 2021
    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

11 authors at 4 institutions in 3 countries.

Takashi YamashitaDepartment of Dermatology, University of Tokyo Graduate School of Medicine, Tokyo, Japan.
Katja LakotaDepartment of Rheumatology, University Medical Centre Ljubljana, Ljubljana, Slovenia.
Takashi TaniguchiDepartment of Dermatology, University of Tokyo Graduate School of Medicine, Tokyo, Japan.
Ayumi YoshizakiDepartment of Dermatology, University of Tokyo Graduate School of Medicine, Tokyo, Japan.
Shinichi SatoDepartment of Dermatology, University of Tokyo Graduate School of Medicine, Tokyo, Japan.
Wen HongNorthwestern Scleroderma Program, Feinberg School of Medicine, Chicago, IL, USA.
Xingchun ZhouNorthwestern Scleroderma Program, Feinberg School of Medicine, Chicago, IL, USA.
Snezn Sodin-SemrlDepartment of Rheumatology, University Medical Centre Ljubljana, Ljubljana, Slovenia.
Feng FangNorthwestern Scleroderma Program, Feinberg School of Medicine, Chicago, IL, USA.
Yoshihide AsanoDepartment of Dermatology, University of Tokyo Graduate School of Medicine, Tokyo, Japan. yasano-tky@umin.ac.jp.ORCID 0000-0001-5560-9778
John VargaNorthwestern Scleroderma Program, Feinberg School of Medicine, Chicago, IL, USA. j-varga@northwestern.edu.
The University of Tokyo · JPScleroderma Foundation · USLjubljana University Medical Centre · SINorthwestern University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The hallmarks of systemic sclerosis (SSc) are autoimmunity, microangiopathy and fibrosis. Skin fibrosis is accompanied by attrition of the dermal white adipose tissue layer, and alterations in the levels and function of adiponectin. Since these findings potentially implicate adiponectin in the pathogenesis of SSc, we employed a novel pharmacological approach to augment adiponectin signaling using AdipoRon, an orally active adiponectin receptor agonist. Chronic treatment with AdipoRon significantly ameliorated bleomycin-induced dermal fibrosis in mice. AdipoRon attenuated fibroblast activation, adipocyte-to-myofibroblast transdifferentiation, Th2/Th17-skewed polarization of the immune response, vascular injury and endothelial-to-mesenchymal transition within the lesional skin. In vitro, AdipoRon abrogated profibrotic responses elicited by TGF-β in normal fibroblasts, and reversed the inherently-activated profibrotic phenotype of SSc fibroblasts. In view of these broadly beneficial effects on all three cardinal pathomechanisms underlying the clinical manifestations of SSc, pharmacological augmentation of adiponectin signaling might represent a novel strategy for the treatment of SSc.

Indexed as

Administration, OralAnimalsBleomycinDisease Models, AnimalFemaleFibrosisHumansInflammationMice, Inbred C57BLPiperidinesReceptors, AdiponectinScleroderma, SystemicSignal TransductionSkinVascular System InjuriesAdipoRonBleomycinPiperidinesReceptors, Adiponectin

Identifiers

PMID30087356
PMCPMC6081386
OpenAlexW2886938658

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.