Evidence map›Paper›PMID 31561418›Full record

ArticleAntioxidants (Basel, Switzerland)2019

Formononetin Upregulates Nrf2/HO-1 Signaling and Prevents Oxidative Stress, Inflammation, and Kidney Injury in Methotrexate-Induced Rats.

Saleem H Aladaileh, Omnia E Hussein, Mohammad H Abukhalil, Sultan A M Saghir, May Bin-Jumah, Manal A Alfwuaires, Mousa O Germoush, Amer A Almaiman, Ayman M Mahmoud

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Antioxidants (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
10.5field-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

70 citing papers in PubMed, 129 citations in OpenAlex.

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10 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 6 institutions in 3 countries.

Saleem H AladailehDepartment of Medical Analysis, Princess Aisha Bint Al-Hussein Faculty of Nursing and Health Sciences, Al-Hussein Bin Talal University, Ma`an 71111, Jordan. sadaileh@ahu.edu.jo.ORCID 0000-0003-2628-6257
Omnia E HusseinPhysiology Division, Department of Zoology, Faculty of Science, Beni-Suef University, Beni-Suef 62514, Egypt. omniaaa411@yahoo.com.
Mohammad H AbukhalilDepartment of Medical Analysis, Princess Aisha Bint Al-Hussein Faculty of Nursing and Health Sciences, Al-Hussein Bin Talal University, Ma`an 71111, Jordan. mabukhalil@ahu.edu.jo.ORCID 0000-0002-4018-6925
Sultan A M SaghirDepartment of Medical Analysis, Princess Aisha Bint Al-Hussein Faculty of Nursing and Health Sciences, Al-Hussein Bin Talal University, Ma`an 71111, Jordan. sultan.s.ayesh@ahu.edu.jo.ORCID 0000-0001-7134-3199
May Bin-JumahDepartment of Biology, College of Science, Princess Nourah bint Abdulrahman University, Riyadh 84428, Saudi Arabia. mnbinjumah@pnu.edu.sa.ORCID 0000-0002-3017-9924
Manal A AlfwuairesDepartment of Biology, Faculty of Science, King Faisal University, Al-Ahsa 31982, Saudi Arabia. malfwuaires@kfu.edu.sa.
Mousa O GermoushDepartment of Biology, College of Science, Jouf University, Sakaka 2014, Saudi Arabia. germoush@ju.edu.sa.
Amer A AlmaimanDepartment of Applied Medical Sciences, Community College of Unaizah, Qassim University, Buraydah 51431, Saudi Arabia. ameralmeman@hotmail.com.
Ayman M MahmoudPhysiology Division, Department of Zoology, Faculty of Science, Beni-Suef University, Beni-Suef 62514, Egypt. ayman.mahmoud@science.bsu.edu.eg.ORCID 0000-0003-0279-6500
Al-Hussein Bin Talal University · JOBeni-Suef University · EGJouf University · SAKing Faisal University · SAPrincess Nourah bint Abdulrahman University · SAQassim University · SA

Funding

Deanship of Scientific Research, Al-Hussein Bin Talal University 198/2019
6 · The paper itself

Abstract

Acute kidney injury (AKI) is a serious complication of methotrexate (MTX). This study explored the protective effect of the isoflavone formononetin (FN) against MTX nephrotoxicity with an emphasis on oxidative stress, inflammation, and nuclear factor (erythroid-derived 2)-like 2/heme oxygenase 1 (Nrf2/HO-1) signaling. Rats received FN (10, 20, and 40 mg/kg) for 10 days and a single dose of MTX on day 7. MTX induced kidney injury was characterized by increased serum creatinine and urea, kidney injury molecule-1 (Kim-1), and several histological alterations. FN ameliorated kidney function and inhibited the renal tissue injury induced by MTX. Reactive oxygen species (ROS), lipid peroxidation (LPO), nitric oxide, and 8-Oxo-2'-deoxyguanosine were increased, whereas antioxidant defenses were diminished in the kidney of MTX-administered rats. In addition, MTX upregulated renal iNOS, COX-2, TNF-α, IL-1β, Bax, caspase-9, and caspase-3, and decreased Bcl-2, Nrf2, and HO-1. FN suppressed oxidative stress, LPO, DNA damage, iNOS, COX-2, proinflammatory cytokines, and apoptosis, and boosted Bcl-2, antioxidants, and Nrf2/HO-1 signaling in MTX-administered rats. In conclusion, FN prevents MTX-induced AKI by activating Nrf2/HO-1 signaling and attenuates oxidative damage and inflammation. Thus, FN may represent an effective adjuvant that can prevent MTX nephrotoxicity, pending further mechanistic studies.

Indexed as

formononetinmethotrexatenephrotoxicityNrf2ROS

Identifiers

PMID31561418
PMCPMC6827027
OpenAlexW2976591098

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.