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

Toxicol Res (Camb)

Department of Pharmacology and Toxicology, Afyon Kocatepe University, Faculty of Veterinary Medicine, Afyonkarahisar 03200, Turkey.

Published: August 2023

AI Article Synopsis

  • 2,4-Dichlorophenoxyacetic acid (2,4-D) and arsenic both pose significant biological toxicity, but their combined effects and mechanisms in co-exposure are not fully understood.
  • A study involving four-week-old female rats showed that co-exposure to both substances for 28 days led to increased biochemical indicators of liver and kidney damage, altered hormonal levels, and evidence of oxidative stress, including lipid peroxidation and decreased antioxidant enzymes.
  • Additionally, significant DNA damage and increased apoptotic and inflammatory markers were observed in co-exposed groups, along with more severe tissue damage compared to exposure to each substance individually.

Article 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 and ) and inflammation (α and ) indexes in the co-exposure groups were markedly increased, whereas the levels of anti-apoptosis index () 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10470338PMC
http://dx.doi.org/10.1093/toxres/tfad047DOI Listing

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