Evidence map›Paper›PMID 40104286›Full record

ArticleTurkish journal of medical sciences2025

Ascorbic acid exhibits more of a protective effect than estradiol against nephrotoxicity induced by malathion in rats: a histopathological and molecular docking study.

Mohammad Alhilal, Mahmoud Elsayed Mohamed Salem, Ahmed Ali Albakoush, Suzan Alhilal, Basant Farag, Sobhi M Gomha

Abstract read
In one paragraph

Article in Turkish journal of medical sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors.

Mohammad AlhilalDepartment of Nursing, Faculty of Health Sciences, Mardin Artuklu University, Mardin, Turkiye.ORCID https://orcid.org/0000-0002-2832-8409
Mahmoud Elsayed Mohamed SalemDepartment of Nursing, Faculty of Health Sciences, Mardin Artuklu University, Mardin, Turkiye.ORCID https://orcid.org/0009-0001-2616-0278
Ahmed Ali AlbakoushDepartment of Pathology, Faculty of Medicine, Alasmarya Islamic University, Zliten, Libya.ORCID https://orcid.org/0000-0001-8037-5651
Suzan AlhilalDepartment of Medical Services and Techniques, Vocational School of Health Services, Mardin Artuklu University, Mardin, Turkiye.ORCID https://orcid.org/0000-0002-9372-9364
Basant FaragDepartment of Chemistry, Faculty of Science, Zagazig University, Zagazig, Egypt.ORCID https://orcid.org/0009-0008-1595-6415
Sobhi M GomhaDepartment of Chemistry, Faculty of Science, Islamic University of Madinah, Madinah, Saudi Arabia.ORCID https://orcid.org/0000-0002-7739-2837

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/aim: Despite the known harmful effects associated with malathion toxicity in various organs, it continues to be widely used for plant protection and insect control. This study is the first to compare the protective effects of estradiol and ascorbic acid against malathion-induced nephrotoxicity through histopathological assessment and molecular docking analyses. Materials and methods: This study was conducted using 20 female albino rats that were distributed into sham, malathion, malathion + estradiol, and malathion + ascorbic acid groups. Nephrotoxicity was induced by daily treatment with malathion and the effects of estradiol and ascorbic on nephrotoxicity were evaluated. After 4 weeks of treatment, the animals were sacrificed and the kidneys were examined following hematoxylin and eosin (H&E) staining. Histopathology results were supported by molecular docking studies of estradiol and ascorbic acid against a target protein (PDB ID: 2YMX), the peptide inhibitor Fab408 inhibiting acetylcholinesterase (AChE). The inhibition of AChE is the primary mechanism of the toxic effects of malathion. Results: Histopathological examination revealed a notable elevation (p < 0.001) in degeneration and necrosis within the tubular epithelium and interstitial nephritis in the malathion group compared to the sham group. Daily administration of estradiol and ascorbic acid resulted in a notable reduction (p = 0.0022) in the severity of these histopathological changes in the malathion + estradiol and malathion + ascorbic acid groups compared to the malathion group. Of these, the most significant decreases were observed in the malathion + ascorbic acid group. Docking studies of these compounds against the selected protein (PDB ID: 2YMX) revealed promising binding scores. Ascorbic acid exhibited the highest docking score (-6.44 kcal/mol), indicating a favorable binding interaction with this protein. Conclusion: Estradiol and ascorbic acid exert protective effects against malathion-induced nephrotoxicity, whereas ascorbic acid showed superior efficacy compared to estradiol. This result was further supported by molecular docking studies.

Indexed as

Ascorbic AcidEstradiolKidneyKidney DiseasesMalathionAnimalsFemaleMolecular Docking SimulationProtective AgentsRatsAscorbic AcidEstradiolMalathionProtective AgentsAscorbic acidestradiolmalathionmolecular dockingnecrosisnephritis

Identifiers

PMID40104286
PMCPMC11913519

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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.