Evidence map›Paper›PMID 31037316›Full record

ArticleInflammation research : official journal of the European Histamine Research Society ... [et al.]2019

Chicoric acid prevents methotrexate-induced kidney injury by suppressing NF-κB/NLRP3 inflammasome activation and up-regulating Nrf2/ARE/HO-1 signaling.

Sanaa M Abd El-Twab, Omnia E Hussein, Walaa G Hozayen, May Bin-Jumah, Ayman M Mahmoud

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In one paragraph

Article in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
11.3field-weighted citation impact, top 1% 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

49 citing papers in PubMed, 98 citations in OpenAlex.

  1. Review
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  7. International journal of molecular sciences · 2025
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  20. Antioxidants (Basel, Switzerland) · 2023
    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

5 authors at 2 institutions in 2 countries.

Sanaa M Abd El-TwabPhysiology Division, Department of Zoology, Faculty of Science, Beni-Suef University, Beni-Suef, Egypt.ORCID http://orcid.org/0000-0003-0279-6500
Omnia E HusseinPhysiology Division, Department of Zoology, Faculty of Science, Beni-Suef University, Beni-Suef, Egypt.
Walaa G HozayenBiochemistry Division, Chemistry Department, Faculty of Science, Beni-Suef University, Beni-Suef, Egypt.
May Bin-JumahDepartment of Biology, College of Science, Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia.
Ayman M MahmoudPhysiology Division, Department of Zoology, Faculty of Science, Beni-Suef University, Beni-Suef, Egypt. ayman.mahmoud@science.bsu.edu.eg.
Beni-Suef University · EGPrincess Nourah bint Abdulrahman University · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveChicoric acid (CA) is a natural product with promising antioxidant and anti-inflammatory properties; however, its protective effect on methotrexate (MTX)-induced acute kidney injury (AKI) hasn't been reported. We investigated the effect of CA on MTX-induced AKI in rats, pointing to the role of NF-κB/NLRP3 inflammasome and Nrf2/ARE/HO-1 signaling. MATERIALS AND

methodsWistar rats received 25 mg/kg and 50 mg/kg CA for 15 days and a single injection of MTX at day 16. At day 19, the rats were killed, and samples were collected for analyses.

resultsMTX induced a significant increase in serum creatinine and urea, and kidney Kim-1, reactive oxygen species (ROS), malondialdehyde and nitric oxide levels. In addition, MTX-induced rats exhibited multiple histopathological alterations, diminished antioxidant defenses, and decreased expression of Nrf2, NQO-1 and HO-1. CA prevented histological alterations, ameliorated kidney function markers, attenuated ROS production and lipid peroxidation, and boosted antioxidant defenses. CA suppressed the expression of NF-κB p65, NLRP3, caspase-1 and IL-1β in the kidney of MTX-induced rats. Furthermore, CA inhibited MTX-induced apoptosis as evidenced by the decreased expression of BAX and caspase-3, and increased Bcl-2 gene expression.

conclusionsCA prevented MTX-induced AKI through activation of Nrf2/ARE/HO-1 signaling, and attenuation of ROS-induced activation of NF-κB/NLRP3 inflammasome signaling.

Indexed as

Acute Kidney InjuryAnimalsAntioxidant Response ElementsApoptosisCaffeic AcidsFolic Acid AntagonistsHeme Oxygenase (Decyclizing)KidneyMaleMethotrexateNF-E2-Related Factor 2NF-kappa BNLR Family, Pyrin Domain-Containing 3 ProteinRats, WistarSignal TransductionSuccinatesCaffeic Acidschicoric acidFolic Acid AntagonistsHeme Oxygenase (Decyclizing)Hmox1 protein, ratMethotrexateNfe2l2 protein, ratNF-E2-Related Factor 2NF-kappa BNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, ratSuccinatesChicoric acidMethotrexateNLRP3 inflammasomeNrf2ROS

Identifiers

PMID31037316
OpenAlexW2943810953

What OpenQuestion holds

Textmetadata
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.