Evidence map›Paper›PMID 35673387›Full record

ArticlePeerJ2022

Quercetin prevents chronic kidney disease on mesangial cells model by regulating inflammation, oxidative stress, and TGF-β1/SMADs pathway.

Wahyu Widowati, Sijani Prahastuti, Rita Tjokropranoto, Philips Onggowidjaja, Hanna Sari Widya Kusuma, Ervi Afifah, Seila Arumwardana, Muhamad Aldi Maulana, Rizal Rizal

Open access · goldAbstract read
In one paragraph

Article in PeerJ, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
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  11. Renoprotective Effects of Brown-StrainInternational journal of molecular sciences · 2024
    Article
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  16. Protective effect of yacon leaves extract (Research in pharmaceutical sciences
    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

9 authors at 2 institutions in 1 country.

Wahyu WidowatiFaculty of Medicine, Maranatha Christian University, Bandung, West Java, Indonesia.
Sijani PrahastutiFaculty of Medicine, Maranatha Christian University, Bandung, West Java, Indonesia.
Rita TjokropranotoFaculty of Medicine, Maranatha Christian University, Bandung, West Java, Indonesia.
Philips OnggowidjajaFaculty of Medicine, Maranatha Christian University, Bandung, West Java, Indonesia.
Hanna Sari Widya KusumaBiomolecular and Biomedical Research Center, Aretha Medika Utama, Bandung, West Java, Indonesia.
Ervi AfifahBiomolecular and Biomedical Research Center, Aretha Medika Utama, Bandung, West Java, Indonesia.
Seila ArumwardanaBiomolecular and Biomedical Research Center, Aretha Medika Utama, Bandung, West Java, Indonesia.
Muhamad Aldi MaulanaBiomolecular and Biomedical Research Center, Aretha Medika Utama, Bandung, West Java, Indonesia.
Rizal RizalBiomolecular and Biomedical Research Center, Aretha Medika Utama, Bandung, West Java, Indonesia.
Maranatha Christian University · IDUniversity of Indonesia · ID

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Chronic kidney disease (CKD) happens due to decreasing kidney function. Inflammation and oxidative stress have been shown to result in the progression of CKD. Quercetin is widely known to have various bioactivities including antioxidant, anticancer, and anti-inflammatory activities. Objective: To evaluate the activity of quercetin to inhibit inflammation, stress oxidative, and fibrosis on CKD cells model (mouse mesangial cells induced by glucose). Methods and Material: The SV40 MES 13 cells were plated in a 6-well plate with cell density at 5,000 cells/well. The medium had been substituted for 3 days with a glucose-induced medium with a concentration of 20 mM. Quercetin was added with 50, 10, and 5 µg/mL concentrations. The negative control was the untreated cell. The levels of TGF-β1, TNF-α, and MDA were determined using ELISA KIT. The gene expressions of the SMAD7, SMAD3, SMAD2, and SMAD4 were analyzed using qRT-PCR. Results: Glucose can lead to an increase in inflammatory cytokines TNF-α, TGF-β1, MDA as well as the expressions of the SMAD2, SMAD3, SMAD4, and a decrease in SMAD7. Quercetin caused the reduction of TNF-α, TGF-β1, MDA as well as the expression of the SMAD2, SMAD3, SMAD4, and increased SMAD7. Conclusion: Quercetin has anti-inflammation, antioxidant, antifibrosis activity in the CKD cells model. Thus, quercetin is a promising substance for CKD therapy and further research is needed to prove this in CKD animal model.

Indexed as

Renal Insufficiency, ChronicTransforming Growth Factor beta1AnimalsAntioxidantsInflammationMesangial CellsMiceOxidative StressQuercetinTumor Necrosis Factor-alphaAntioxidantsQuercetinTransforming Growth Factor beta1Tumor Necrosis Factor-alphaAnti-inflammationAntioxidantChronic kidney diseaseQuercetin

Identifiers

PMID35673387
PMCPMC9167587
OpenAlexW4281637778

What OpenQuestion holds

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LicenceCC BY
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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.