Synergistic toxicity of 2,4-dichlorophenoxyacetic acid and arsenic alters biomarkers in rats
| dc.contributor.author | Demirel, Hasan Huseyin | |
| dc.contributor.author | Zemheri Navruz, Fahriye | |
| dc.contributor.author | Kucukkurt, Ismail | |
| dc.contributor.author | Arslan-Acaroz, Damla | |
| dc.contributor.author | Tureyen, Ali | |
| dc.contributor.author | Ince, Sinan | |
| dc.contributor.author | Navruz, Fahriye Zemheri | |
| dc.date.accessioned | 2025-10-18T10:02:41Z | |
| dc.date.created | 2023 | |
| dc.date.issued | 2023 | |
| dc.department | Fakülteler, Fen Fakültesi, Moleküler Biyoloji ve Genetik Bölümü | |
| dc.description.abstract | 2,4-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.sponsorship | Afyon Kocatepe University Scientific Research Council of Turkey [17] | |
| dc.description.sponsorship | This study was financially supported by a grant (Project No: 17.KARIYER.179) from the Afyon Kocatepe University Scientific Research Council of Turkey. | |
| dc.identifier.doi | 10.1093/toxres/tfad047 | |
| dc.identifier.endpage | 583 | |
| dc.identifier.issn | 2045-452X | |
| dc.identifier.issn | 2045-4538 | |
| dc.identifier.issue | 4 | |
| dc.identifier.orcid | Ince, Sinan/0000-0002-1915-9797 | |
| dc.identifier.orcid | KUCUKKURT, ISMAIL/0000-0003-0198-629X; | |
| dc.identifier.pmid | 37663805 | |
| dc.identifier.startpage | 574 | |
| dc.identifier.uri | https://doi.org/10.1093/toxres/tfad047 | |
| dc.identifier.uri | https://hdl.handle.net/11772/20724 | |
| dc.identifier.volume | 12 | |
| dc.identifier.wos | WOS:001013019100001 | |
| dc.identifier.wosquality | Q3 | |
| dc.indekslendigikaynak | Web of Science | |
| dc.indekslendigikaynak | PubMed | |
| dc.language.iso | en | |
| dc.publisher | Oxford Univ Press | |
| dc.relation.ispartof | Toxicology Research | |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.snmz | WoS_20251016 | |
| dc.subject | 2, 4-Dichlorophenoxyacetic | |
| dc.subject | Arsenic | |
| dc.subject | Dna Damage | |
| dc.subject | Inflammation | |
| dc.subject | Apoptosis | |
| dc.subject | Rat | |
| dc.title | Synergistic toxicity of 2,4-dichlorophenoxyacetic acid and arsenic alters biomarkers in rats | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| relation.isAuthorOfPublication | f79ec742-baba-48be-89fc-10f7ded30e19 | |
| relation.isAuthorOfPublication.latestForDiscovery | f79ec742-baba-48be-89fc-10f7ded30e19 |










