Evidence map›Paper›PMID 33379332›Full record

ArticleInternational journal of molecular sciences2020

Kaempferol Inhibits Zearalenone-Induced Oxidative Stress and Apoptosis via the PI3K/Akt-Mediated Nrf2 Signaling Pathway: In Vitro and In Vivo Studies.

Peramaiyan Rajendran, Rebai Ben Ammar, Fatma J Al-Saeedi, Maged E Mohamed, Medhat A ElNaggar, Saeed Y Al-Ramadan, Gamal M Bekhet, Ahmed M Soliman

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
15.8field-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

58 citing papers in PubMed, 111 citations in OpenAlex.

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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

8 authors at 5 institutions in 4 countries.

Peramaiyan RajendranDepartment of Biological Sciences, College of Science, King Faisal University, Al-Ahsa 31982, Saudi Arabia.ORCID 0000-0001-6354-4388
Rebai Ben AmmarDepartment of Biological Sciences, College of Science, King Faisal University, Al-Ahsa 31982, Saudi Arabia.ORCID 0000-0002-9454-6295
Fatma J Al-SaeediDepartment of Nuclear Medicine, Faculty of Medicine, Kuwait University, Safat 13110, Kuwait.ORCID 0000-0003-0932-6261
Maged E MohamedPharmaceutical Sciences Department, College of Clinical Pharmacy, King Faisal University, Al-Ahsa 31982, Saudi Arabia.
Medhat A ElNaggarPlant Pathology Research Institute, Agricultural Research Center, Giza Governorate 12619, Egypt.ORCID 0000-0002-8914-5091
Saeed Y Al-RamadanDepartment of Anatomy, College of Veterinary Medicine, King Faisal University, Al-Ahsa 31982, Saudi Arabia.
Gamal M BekhetDepartment of Biological Sciences, College of Science, King Faisal University, Al-Ahsa 31982, Saudi Arabia.
Ahmed M SolimanDepartment of Arid Land Agriculture, College of Agricultural & Food Sciences, King Faisal University, Al Ahsa 31982, Saudi Arabia.ORCID 0000-0001-7896-8538
King Faisal University · SAAgricultural Research Center · EGCenter of Biotechnogy of Borj Cédria · TNKuwait University · KWZagazig University · EG

Funding

The Deputyship ‎for Research & Innovation, Ministry of Education in the Kingdom ‎Saudi Arabia IFT20091
6 · The paper itself

Abstract

In this study, kaempferol (KFL) shows hepatoprotective activity against zearalenone (ZEA)-induced oxidative stress and its underlying mechanisms in in vitro and in vivo models were investigated. Oxidative stress plays a critical role in the pathophysiology of various hepatic ailments and is normally regulated by reactive oxygen species (ROS). ZEA is a mycotoxin known to exert toxicity via inflammation and ROS accumulation. This study aims to explore the protective role of KFL against ZEA-triggered hepatic injury via the PI3K/Akt-regulated Nrf2 pathway. KFL augmented the phosphorylation of PI3K and Akt, which may stimulate antioxidative and antiapoptotic signaling in hepatic cells. KFL upregulated Nrf2 phosphorylation and the expression of antioxidant genes HO-1 and NQO-1 in a dose-dependent manner under ZEA-induced oxidative stress. Nrf2 knockdown via small-interfering RNA (siRNA) inhibited the KFL-mediated defence against ZEA-induced hepatotoxicity. In vivo studies showed that KFL decreased inflammation and lipid peroxidation and increased H

Indexed as

Signal TransductionAnimalsApoptosisBiomarkersCytokinesDNA DamageGene Knockdown TechniquesHeme Oxygenase-1Hep G2 CellsHumansInflammation MediatorsKaempferolsLipid PeroxidationLiverMaleMiceBiomarkersCytokinesHeme Oxygenase-1Inflammation MediatorskaempferolKaempferolsNAD(P)H Dehydrogenase (Quinone)NF-E2-Related Factor 2NQO1 protein, humanPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktReactive Oxygen SpeciesZearalenoneapoptosishepatotoxicitykaempferolNrf2PI3K/Aktzearalenone

Identifiers

PMID33379332
PMCPMC7794799
OpenAlexW3115309851

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.