Evidence map›Paper›PMID 36342062›Full record

ArticleRedox report : communications in free radical research2022

Zinc oxide nanoparticles and spironolactone-enhanced Nrf2/HO-1 pathway and inhibited Wnt/β-catenin pathway in adenine-induced nephrotoxicity in rats.

Amira Awadalla, Eman T Hamam, Fardous F El-Senduny, Nisreen Mansour Omar, Mohamed R Mahdi, Nashwa Barakat, Omar A Ammar, Abdelaziz M Hussein, Ahmed A Shokeir, Salma M Khirallah

Open access · goldAbstract read
In one paragraph

Article in Redox report : communications in free radical research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.3field-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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Nanotherapeutics in Kidney Disease: Innovations, Challenges, and Future Directions.Journal of the American Society of Nephrology : JASN · 2025
    Review
  5. Review
  6. Review
  7. Review
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

10 authors at 3 institutions in 2 countries.

Amira AwadallaCenter of Excellence for Genome and Cancer Research, Urology and Nephrology Center, Mansoura University, Mansoura, Egypt.
Eman T HamamCenter of Excellence for Genome and Cancer Research, Urology and Nephrology Center, Mansoura University, Mansoura, Egypt.
Fardous F El-SendunyChemistry Department, Faculty of Science, Mansoura University, Mansoura, Egypt.
Nisreen Mansour OmarDepartment of Medical Physiology, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Mohamed R MahdiDepartment of Human Anatomy and Embryology, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Nashwa BarakatUrology and Nephrology Center, Mansoura University, Mansoura, Egypt.
Omar A AmmarBasic Science Department, Delta University for Science and Technology, Gamasa, Egypt.
Abdelaziz M HusseinDepartment of Medical Physiology, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Ahmed A ShokeirCenter of Excellence for Genome and Cancer Research, Urology and Nephrology Center, Mansoura University, Mansoura, Egypt.
Salma M KhirallahBiochemistry Division, Chemistry Department, Faculty of Science, Port Said University, Port Said, Egypt.ORCID 0000-0002-7631-6840
Mansoura University · EGDelta University for Science and Technology · EGPort Said University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate the renoprotective, the antioxidant, and the anti-inflammatory impact of a combination of SPL and ZnO-NPs to combat against chronic kidney disease (CKD).

methodsIn total, 50 males of rats were distributed into 5 groups (10 rats each); normal group, adenine sulfate (0.25% in diet for 10 days) (CKD) group. After the last dose of adenine sulfate, rats were divided into three groups: SPL + Adenine sulfate group; rats were treated orally by mixing SPL (20 mg/kg/day) into chow for 8 weeks, ZnO-NPs + Adenine sulfate group; rats were injected intraperitoneally with ZnO-NPs (5 mg/kg) three times weekly for 8 weeks, ZnO-NPs + SPL + Adenine sulfate group; rats were injected with the same previous doses for 8 weeks.

resultsEach of SPL and ZnO-NPs up-regulated antioxidant genes (

conclusionThe therapeutic role of SPL was enhanced by the antioxidant and the anti-inflammatory role of ZnO-NPs, which presented a great renoprotective effect against CKD.

Indexed as

NanoparticlesRenal Insufficiency, ChronicZinc OxideAdenineAnimalsAnti-Inflammatory AgentsAntioxidantsbeta CateninMaleNF-E2-Related Factor 2RatsSpironolactoneSulfatesAdenineAnti-Inflammatory AgentsAntioxidantsbeta CateninNF-E2-Related Factor 2SpironolactoneSulfatesZinc OxideCKDHO-1NephrotoxicityNrf2spironolactoneWntZnO-NPsβ-catenin

Identifiers

PMID36342062
PMCPMC9648381
OpenAlexW4308439071

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.