Evidence map›Paper›PMID 23819014›Full record

ArticleOxidative medicine and cellular longevity2013

Resveratrol suppresses PAI-1 gene expression in a human in vitro model of inflamed adipose tissue.

Ivana Zagotta, Elitsa Y Dimova, Jan-Bernd Funcke, Martin Wabitsch, Thomas Kietzmann, Pamela Fischer-Posovszky

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.3field-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

19 citing papers in PubMed, 33 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Article
  6. Role of TGF-β1/SMADs signalling pathway in resveratrol-induced reduction of extracellular matrix deposition by dexamethasone-treated human trabecular meshwork cells.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2024
    Article
  7. SARS-CoV-2 Infection Alters the Phenotype and Gene Expression of Adipocytes.International journal of molecular sciences · 2024
    Article
  8. Review
  9. PAI-1, the Plasminogen System, and Skeletal Muscle.International journal of molecular sciences · 2020
    Review
  10. Triterpenoids Extracted FromFrontiers in microbiology · 2020
    Article
  11. Article
  12. The Effects of Resveratrol in the Treatment of Metabolic Syndrome.International journal of molecular sciences · 2019
    Review
  13. Article
  14. Article
  15. Article
  16. PAI-1 and TNF-α profiles of adipose tissue in obese cardiovascular disease patients.International journal of clinical and experimental pathology · 2015
    Article
  17. Article
  18. Review
  19. 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

6 authors at 2 institutions in 2 countries.

Ivana ZagottaDivision of Pediatric Endocrinology and Diabetes, Department of Pediatrics and Adolescent Medicine, Ulm University Medical Center, Ulm, Germany.
Elitsa Y Dimova
Jan-Bernd Funcke
Martin Wabitsch
Thomas Kietzmann
Pamela Fischer-Posovszky
Universität Ulm · DEUniversity of Oulu · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Increased plasminogen activator inhibitor-1 (PAI-1) levels are associated with a number of pathophysiological complications; among them is obesity. Resveratrol was proposed to improve obesity-related health problems, but the effect of resveratrol on PAI-1 gene expression in obesity is not completely understood. In this study, we used SGBS adipocytes and a model of human adipose tissue inflammation to examine the effects of resveratrol on the production of PAI-1. Treatment of SGBS adipocytes with resveratrol reduced PAI-1 mRNA and protein in a time- and concentration-dependent manner. Further experiments showed that obesity-associated inflammatory conditions lead to the upregulation of PAI-1 gene expression which was antagonized by resveratrol. Although signaling via PI3K, Sirt1, AMPK, ROS, and Nrf2 appeared to play a significant role in the modulation of PAI-1 gene expression under noninflammatory conditions, those signaling components were not involved in mediating the resveratrol effects on PAI-1 production under inflammatory conditions. Instead, we demonstrate that the resveratrol effects on PAI-1 induction under inflammatory conditions were mediated via inhibition of the NF κ B pathway. Together, resveratrol can act as NF κ B inhibitor in adipocytes and thus the subsequently reduced PAI-1 expression in inflamed adipose tissue might provide a new insight towards novel treatment options of obesity.

Indexed as

Models, BiologicalAdipocytesAdipose TissueAMP-Activated Protein KinasesAnimalsArrhythmias, CardiacCulture Media, ConditionedDNADown-RegulationFemaleGene Expression RegulationGenetic Diseases, X-LinkedGigantismHeart Defects, CongenitalHumansInflammationAMP-Activated Protein KinasesCulture Media, ConditionedDNANF-E2-Related Factor 2NF-kappa BPhosphatidylinositol 3-KinasesPlasminogen Activator Inhibitor 1Reactive Oxygen SpeciesResveratrolRNA, MessengerSirtuin 1Stilbenes

Identifiers

PMID23819014
PMCPMC3684090
OpenAlexW2080744941

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.