Synergistic toxicity of 2,4-dichlorophenoxyacetic acid and arsenic alters biomarkers in rats.
Hasan Huseyin DemirelFahriye Zemheri-Navruzİsmail KucukkurtDamla Arslan-AcarozAli TureyenSinan IncePublished in: Toxicology research (2023)
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 ( NFκB, Cox-2, TNF- α , and TGFβI ) 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.
Keyphrases
- oxidative stress
- drinking water
- dna damage
- induced apoptosis
- cell death
- heavy metals
- health risk
- health risk assessment
- diabetic rats
- ischemia reperfusion injury
- dna repair
- gene expression
- signaling pathway
- type diabetes
- early onset
- rheumatoid arthritis
- endoplasmic reticulum stress
- cell cycle arrest
- epithelial mesenchymal transition
- single cell
- uric acid
- heat shock
- gram negative
- immune response
- lps induced
- polycystic ovary syndrome