Publication:
Synthetic Pyrethroids Common Metabolite 3-Phenoxybenzoic Acid Induces Caspase-3 and Bcl-2 Mediated Apoptosis in Human Hepatocyte Cells

dc.authorscopusid16238460900
dc.authorscopusid57205638269
dc.authorscopusid57215684606
dc.authorscopusid57222387579
dc.authorscopusid56353804300
dc.authorwosidGuvenc, Tolga/Aag-4599-2019
dc.authorwosidKuruca, Nilufer/Nft-5949-2025
dc.authorwosidİnal, Sinem/Aag-5033-2019
dc.contributor.authorGuvenc, Dilek
dc.contributor.authorInal, Sinem
dc.contributor.authorKuruca, Nilufer
dc.contributor.authorGokmen, Sedat
dc.contributor.authorGuvenc, Tolga
dc.contributor.authorIDKuruca, Nilufer/0000-0001-5601-4952
dc.contributor.authorIDInal, Sinem/0000-0002-2552-5159
dc.contributor.authorIDGuvenc, Tolga/0000-0003-1468-3415
dc.date.accessioned2025-12-11T01:27:00Z
dc.date.issued2022
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Guvenc, Dilek] Univ Ondokuz Mayis, Fac Vet Med, Dept Pharmacol & Toxicol, Samsun, Turkey; [Inal, Sinem; Kuruca, Nilufer; Guvenc, Tolga] Univ Ondokuz Mayis, Fac Vet Med, Dept Pathol, Samsun, Turkey; [Gokmen, Sedat] Amasya Univ, Suluova Vocat Sch, Dept Laborant & Vet Hlth, Amasya, Turkeyen_US
dc.descriptionKuruca, Nilufer/0000-0001-5601-4952; Inal, Sinem/0000-0002-2552-5159; Guvenc, Tolga/0000-0003-1468-3415en_US
dc.description.abstractSynthetic pyrethroids are a group of insecticides frequently used in public health and agriculture, and 3-PBA is a common metabolite of them. Although the liver is the primary organ responsible for metabolizing many compounds including pesticides, to the authors' knowledge there have been no studies on the direct hepatotoxic effects of 3-PBA. Therefore, this study aimed to investigate the possible hepatotoxic effects of 3-PBA on a Human Hepatoma Cell Line (HepG2) and the underlying apoptotic mechanisms. Firstly, an LC50 of 1041.242 mu M was calculated for 3-PBA by using the WST-1 test with concentrations ranging between 1 mu M and 10 mM. Following that, the HepG2 cells in the experimental group were exposed to 3 different concentrations of 3-PBA (1/5 LC50, 1/10 LC50 and 1/20 LC50) for 24 hours. The apoptotic mechanism was evaluated by using flow cytometry, and immunofluorescence assays for Caspase 3 and Bcl-2. In the flow cytometry assay, the total number of apoptotic cells increased in a dose dependent manner (p < 0.05). In the immunofluorescence assay, the Caspase 3 protein showed strong immunoreactivity in the experimental groups, while the reaction to the Bcl-2 protein was minimal. These results demonstrated that 3-PBA has a significant hepatotoxic effect on HepG2 cells and induces apoptosis via the regulation of Caspase-3 and Bcl-2. Furthermore, our results could further the understanding of the fundamental molecular mechanisms of 3-PBA hepatotoxicity. More studies are needed to determine the effects of long-term exposure to 3-PBA and also the molecular mechanisms underlying hepatotoxicity.en_US
dc.description.woscitationindexScience Citation Index Expanded
dc.identifier.doi10.1080/01480545.2021.1894720
dc.identifier.endpage1977en_US
dc.identifier.issn0148-0545
dc.identifier.issn1525-6014
dc.identifier.issue5en_US
dc.identifier.pmid33706615
dc.identifier.scopus2-s2.0-85102558904
dc.identifier.scopusqualityQ2
dc.identifier.startpage1971en_US
dc.identifier.urihttps://doi.org/10.1080/01480545.2021.1894720
dc.identifier.urihttps://hdl.handle.net/20.500.12712/43812
dc.identifier.volume45en_US
dc.identifier.wosWOS:000628088800001
dc.identifier.wosqualityQ3
dc.language.isoenen_US
dc.publisherTaylor & Francis Ltden_US
dc.relation.ispartofDrug and Chemical Toxicologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject3-Phenoxybenzoic Aciden_US
dc.subjectHepatotoxicityen_US
dc.subjectCaspase-3en_US
dc.subjectBcl-2en_US
dc.subjectApoptosisen_US
dc.titleSynthetic Pyrethroids Common Metabolite 3-Phenoxybenzoic Acid Induces Caspase-3 and Bcl-2 Mediated Apoptosis in Human Hepatocyte Cellsen_US
dc.typeArticleen_US
dspace.entity.typePublication

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