Evidence map›Paper›PMID 30483779›Full record

ArticleMolecular medicine reports2019

Visfatin is regulated by interleukin‑6 and affected by the PPAR‑γ pathway in BeWo cells.

Yanhong Zhang, Yan Huo, Wenhui He, Suxin Liu, Hongyan Li, Li Li

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 21% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
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  3. Review
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  5. Review
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  7. Article
  8. Review
  9. Role of visfatin in obesity-induced insulin resistance.World journal of clinical cases · 2022
    Review
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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 1 country.

Yanhong ZhangDepartment of Obstetrics, Hebei General Hospital, Shijiazhuang, Hebei 050051, P.R. China.
Yan HuoDepartment of Obstetrics, Hebei General Hospital, Shijiazhuang, Hebei 050051, P.R. China.
Wenhui HeDepartment of Obstetrics, Cangzhou People's Hospital, Cangzhou, Hebei 061000, P.R. China.
Suxin LiuDepartment of Obstetrics, Hebei General Hospital, Shijiazhuang, Hebei 050051, P.R. China.
Hongyan LiDepartment of Obstetrics, Hebei General Hospital, Shijiazhuang, Hebei 050051, P.R. China.
Li LiDepartment of Obstetrics, Hebei General Hospital, Shijiazhuang, Hebei 050051, P.R. China.
Hebei General Hospital · CNPeople's Hospital of Cangzhou · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Visfatin, an adipocytokine and cytosolic enzyme with nicotinamide phosphoribosyltransferase (Nampt) activity, is involved in the pathogenesis of numerous metabolic disorders. In addition, the nuclear receptor peroxisome proliferator‑activated receptor‑γ (PPAR‑γ) serves important roles in anti‑inflammatory reactions and regulates glucose and lipid metabolism. The aim of the present study was to investigate the effect of interleukin‑6 (IL‑6) on the expression and secretion of visfatin in BeWo cells, and to determine whether the PPAR‑γ pathway is involved in the regulation of visfatin by IL‑6. Therefore, BeWo cells were stimulated with serial concentrations of IL‑6 or pioglitazone, and the expression levels of visfatin and PPAR‑γ were determined by reverse transcription‑quantitative polymerase chain reaction and western blotting. The results of the present study demonstrated that IL‑6 downregulated the mRNA levels of visfatin and PPAR‑γ, which were strongly associated. Activation of PPAR‑γ by pioglitazone resulted in significantly increased expression of visfatin, which abrogated the inhibitory effect of IL‑6 on visfatin in BeWo cells. Furthermore, treatment using pioglitazone alone increased the expression and secretion of the visfatin protein, compared with the control or IL‑6 alone group. In summary, the findings of the present study suggested that IL‑6 inhibited the expression of visfatin and PPAR‑γ at the transcriptional level; in addition, activation of PPAR‑γ upregulated visfatin at the mRNA and protein expression levels. Therefore, the PPAR‑γ signaling pathway may be involved in the regulation of visfatin by IL‑6 in BeWo cells. These results may provide novel insight into the roles of visfatin in trophoblastic cells. Furthermore, thiazolidinedione pioglitazone, by upregulating visfatin expression, may promote the energy metabolism of trophoblastic cells, maintain the function of the placenta and improve the outcome of pregnancy.

Indexed as

Cells, CulturedCytokinesDown-RegulationHumansInterleukin-6Nicotinamide PhosphoribosyltransferasePPAR gammaRNA, MessengerSignal TransductionTranscription, GeneticTrophoblastsUp-RegulationCytokinesIL6 protein, humanInterleukin-6Nicotinamide Phosphoribosyltransferasenicotinamide phosphoribosyltransferase, humanPPAR gammaRNA, MessengerIL-6inflammationNamptPPAR-γvisfatin

Identifiers

PMID30483779
PMCPMC6297763
OpenAlexW2900936180

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.