Evidence map›Paper›PMID 42472891›Full record

ArticleScientific reports2026

Comparative study on the pulmonary toxicity induced by some marketed pesticides after repeated oral administration in rats.

Eman I Hassanen, Marwa A Ibrahim, Shaimaa Kamel

Abstract readComparative Study
In one paragraph

Article in Scientific reports, 2026. 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

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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

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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

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

3 authors.

Eman I HassanenDepartment of Pathology, Faculty of Veterinary Medicine, Cairo University, Giza, Egypt.
Marwa A IbrahimDepartment of Biochemistry and Molecular Biology, Faculty of Veterinary Medicine, Cairo University, P.O. Box 12211, Giza, Egypt. marwaibrahim@cu.edu.eg.ORCID 0000-0001-7935-8379
Shaimaa KamelDepartment of Biochemistry and Molecular Biology, Faculty of Veterinary Medicine, Cairo University, P.O. Box 12211, Giza, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mancozeb (MC), carbendazim (CBZ), and hymexazol (HML) are widely used fungicides in agricultural and veterinary fields worldwide. Our goal is to compare the pulmonary toxicity induced by oral gavage of these pesticides in rats. Thirty-five rats were used and divided into 7 groups as follows: (1) control negative, (2, 3) 125 and 250 mg/kg. bwt MC, respectively, (4, 5) 125, 250 mg/kg. bwt CBZ, respectively, (6, 7) 75, 150 mg/kg. bwt HML, respectively. All treatments were given to rats daily via oral routes for 14 days. All of these fungicides dose-dependently increased MDA levels and decreased GSH content in lung tissue homogenates. The oral intake of these fungicides could upregulate the mRNA levels of IL1β, TNFα, and NF-κB genes and exhibit strong iNOS and Cox-2 protein expressions along with severe histopathological alterations within the pulmonary tissues. The highest pulmonary toxicity was recorded in the HML groups, followed by the MC and CBZ groups. The oral intake of these fungicides dose-dependently induced pulmonary toxicity via oxidative stress, which is associated with triggering the NF-κB signaling pathway.

Indexed as

Fungicides, IndustrialLungPesticidesAdministration, OralAnimalsBenzimidazolesCarbamatesCyclooxygenase 2GlutathioneInterleukin-1betaMaleMalondialdehydeManebNF-kappa BNitric Oxide Synthase Type IIOxidative StressBenzimidazolesCarbamatescarbendazimCyclooxygenase 2Fungicides, IndustrialGlutathioneInterleukin-1betaMalondialdehydemancozebManebNF-kappa BNitric Oxide Synthase Type IIPesticidesTumor Necrosis Factor-alphaZinebGene expressionInflammationOxidative stressPesticidesPulmonary toxicity

Identifiers

PMID42472891
PMCPMC13381874

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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.