Synergistic toxicity of 2,4-dichlorophenoxyacetic acid and arsenic alters biomarkers in rats

dc.contributor.authorDemirel, Hasan Huseyin
dc.contributor.authorZemheri Navruz, Fahriye
dc.contributor.authorKucukkurt, Ismail
dc.contributor.authorArslan-Acaroz, Damla
dc.contributor.authorTureyen, Ali
dc.contributor.authorInce, Sinan
dc.contributor.authorNavruz, Fahriye Zemheri
dc.date.accessioned2025-10-18T10:02:41Z
dc.date.created2023
dc.date.issued2023
dc.departmentFakülteler, Fen Fakültesi, Moleküler Biyoloji ve Genetik Bölümü
dc.description.abstract2,4-dichlorophenoxyacetic acid (2,4-D) and arsenic cause severe and extensive biological toxicity in organisms. However, their interactions and toxic mechanisms in co-exposure remain to be fully elucidated. In this study, 28 four-week-old female rats were divided into four groups and exposed to 100 mg/L arsenic or/and 600 mg/L 2,4-D through drinking water for a period of 28 days. As a result, it was revealed that biochemical indicators (ALT, AST, ALP, blood urea nitrogen, and creatinine) were increased and decreased hormonal parameters (FSH, LH, PG, and E2) in arsenic and 2,4-D and arsenic combination-treated groups. Moreover, increased lipid peroxidation (malondialdehyde level) and decreased antioxidant status (superoxide dismutase and catalase activities) were found in the co-exposure groups compared with the individual-exposure groups. Meanwhile, severe DNA damage was observed in co-exposure groups. Additionally, the levels of apoptotic (Bax, Caspase-3, Caspase-8, Caspase-9, p53, and PARP) and inflammation (NF kappa B, Cox-2, TNF-alpha, and TGF beta I) indexes in the co-exposure groups were markedly increased, whereas the levels of anti-apoptosis index (Bcl-2) were decreased. It was also observed that co-exposure with 2,4-D and arsenic caused more histopathological changes in tissues. Generally, these results show that co-exposure to 2,4-D and arsenic can seriously cause oxidative stress, DNA damage, apoptosis and inflammation while having toxicological risk for organisms. [GRAPHICS] .
dc.description.sponsorshipAfyon Kocatepe University Scientific Research Council of Turkey [17]
dc.description.sponsorshipThis study was financially supported by a grant (Project No: 17.KARIYER.179) from the Afyon Kocatepe University Scientific Research Council of Turkey.
dc.identifier.doi10.1093/toxres/tfad047
dc.identifier.endpage583
dc.identifier.issn2045-452X
dc.identifier.issn2045-4538
dc.identifier.issue4
dc.identifier.orcidInce, Sinan/0000-0002-1915-9797
dc.identifier.orcidKUCUKKURT, ISMAIL/0000-0003-0198-629X;
dc.identifier.pmid37663805
dc.identifier.startpage574
dc.identifier.urihttps://doi.org/10.1093/toxres/tfad047
dc.identifier.urihttps://hdl.handle.net/11772/20724
dc.identifier.volume12
dc.identifier.wosWOS:001013019100001
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherOxford Univ Press
dc.relation.ispartofToxicology Research
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzWoS_20251016
dc.subject2, 4-Dichlorophenoxyacetic
dc.subjectArsenic
dc.subjectDna Damage
dc.subjectInflammation
dc.subjectApoptosis
dc.subjectRat
dc.titleSynergistic toxicity of 2,4-dichlorophenoxyacetic acid and arsenic alters biomarkers in rats
dc.typeArticle
dspace.entity.typePublication
relation.isAuthorOfPublicationf79ec742-baba-48be-89fc-10f7ded30e19
relation.isAuthorOfPublication.latestForDiscoveryf79ec742-baba-48be-89fc-10f7ded30e19

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