Evidence map›Paper›PMID 29849865›Full record

ArticleOxidative medicine and cellular longevity2018

VDR Agonist Prevents Diabetic Endothelial Dysfunction through Inhibition of Prolyl Isomerase-1-Mediated Mitochondrial Oxidative Stress and Inflammation.

Meijin Zhang, Liming Lin, Changsheng Xu, Dajun Chai, Feng Peng, Jinxiu Lin

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Review
  3. Emerging role of vitamin DAnimal nutrition (Zhongguo xu mu shou yi xue hui) · 2024
    Article
  4. Review
  5. The molecular mechanisms of peptidyl-prolylFrontiers in pharmacology · 2024
    Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Vitamin DFrontiers in immunology · 2022
    Article
  11. Review
  12. Observational
  13. Article
  14. Juglone in Oxidative Stress and Cell Signaling.Antioxidants (Basel, Switzerland) · 2019
    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

6 authors at 1 institution in 1 country.

Meijin Zhang *The First Clinical Medical College, Fujian Medical University, Fuzhou, Fujian, China.ORCID 0000-0003-2925-1228
Liming Lin *The First Clinical Medical College, Fujian Medical University, Fuzhou, Fujian, China.ORCID 0000-0002-0259-5269
Changsheng XuFujian Provincial Institute of Hypertension, the First Affiliated Hospital, Fujian Medical University, Fuzhou, Fujian, China.
Dajun ChaiDepartment of Cardiology, the First Affiliated Hospital, Fujian Medical University, Fuzhou, Fujian, China.ORCID 0000-0001-9477-9956
Feng PengDepartment of Cardiology, the First Affiliated Hospital, Fujian Medical University, Fuzhou, Fujian, China.ORCID 0000-0001-6839-3478
Jinxiu LinDepartment of Cardiology, the First Affiliated Hospital, Fujian Medical University, Fuzhou, Fujian, China.ORCID 0000-0003-1035-2993
Fujian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimUpregulation of prolyl isomerase-1 (Pin1) protein expression and activity was associated with the pathogenesis of diabetic vasculopathy through induction of endothelial oxidative stress and inflammation. Moreover, VDR agonist protects against high glucose-induced endothelial apoptosis through the inhibition of oxidative stress. We aimed to explore the effects of the VDR agonist on diabetes-associated endothelial dysfunction and the role of Pin1 in this process.

methodsStreptozocin-induced diabetic mice were randomly treated with vehicle, VDR agonist (10

resultsBoth VDR agonist and Juglone significantly improved diabetes-associated endothelial dysfunction and reduced high glucose-induced endothelial apoptosis. Mechanistically, the circulatory levels of SOD and NO were increased compared with those of vehicle-treated diabetic mice. Additionally, Pin1 protein expression and activity, p66Shc mitochondrial translocation, and NF-

conclusionsVDR agonist prevents diabetic endothelial dysfunction through inhibition of Pin1-mediated mitochondrial oxidative stress and inflammation.

Indexed as

AnimalsDiabetes Mellitus, ExperimentalDisease Models, AnimalEndothelium, VascularHumansInflammationMaleMiceMitochondriaOxidative StressPeptidylprolyl IsomeraseReceptors, CalcitriolTransfectionPeptidylprolyl IsomeraseReceptors, CalcitriolVDR protein, human

Identifiers

PMID29849865
PMCPMC5925189
OpenAlexW2798195560

What OpenQuestion holds

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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.