Interactive renal toxicity of perfluorooctanoic acid and ethanol: Impairment of epithelial transport and redox homeostasis in male Sprague–Dawley rats

-ATPase-specifically localized within the renal tubules. This suppression was significantly more pronounced in the co-exposure group than in the PFOA-only group. Furthermore, a significant decrease in E-cadherin expression, without a robust increase in N-cadherin, indicated early-stage epithelial instability and compromised barrier integrity rather than a full mesenchymal transition. Notably, this structural remodeling was accompanied by an atypical suppression of redox homeostasis, evidenced by the simultaneous decline in catalase and 4-hydroxynonenal (4-HNE) levels, suggesting a state of metabolic depression. Collectively, our findings demonstrate that the interaction between PFOA and EtOH exacerbates subclinical renal vulnerability by dismantling tubular transport and structural frameworks. This study underscores the critical importance of incorporating pollutant-lifestyle interactions and internal dosimetry into future mixture-based risk assessment frameworks.

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Publication Details

Journal
Environmental Pollution
Published
2026-04-16
DOI
https://doi.org/10.1016/j.envpol.2026.128155
Primary Topic
Per- and polyfluoroalkyl substances research
Type
article
Field-Weighted Citation Impact
0.00

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article

Interactive renal toxicity of perfluorooctanoic acid and ethanol: Impairment of epithelial transport and redox homeostasis in male Sprague–Dawley rats

Min Heui Yoo, Byoung‐Seok Lee, Sang-Jin Park, Quy Thi Nguyen et al.
Environmental Pollution
Per- and polyfluoroalkyl substances research
article

Interactive renal toxicity of perfluorooctanoic acid and ethanol: Impairment of epithelial transport and redox homeostasis in male Sprague–Dawley rats

Min Heui Yoo, Byoung‐Seok Lee, Sang-Jin Park, Quy Thi Nguyen, Wan-Jung Im, Yong-Bum Kim
article en

Abstract

-ATPase-specifically localized within the renal tubules. This suppression was significantly more pronounced in the co-exposure group than in the PFOA-only group. Furthermore, a significant decrease in E-cadherin expression, without a robust increase in N-cadherin, indicated early-stage epithelial instability and compromised barrier integrity rather than a full mesenchymal transition. Notably, this structural remodeling was accompanied by an atypical suppression of redox homeostasis, evidenced by the simultaneous decline in catalase and 4-hydroxynonenal (4-HNE) levels, suggesting a state of metabolic depression. Collectively, our findings demonstrate that the interaction between PFOA and EtOH exacerbates subclinical renal vulnerability by dismantling tubular transport and structural frameworks. This study underscores the critical importance of incorporating pollutant-lifestyle interactions and internal dosimetry into future mixture-based risk assessment frameworks.

Environmental PollutionVol. 399
Korea Institute of Toxicology (KR), Korea University of Science and Technology (KR)
Korea Institute of Toxicology, Ministry of Science and ICT, South Korea
Zero hunger
Openalex Percentile: Top 25%
Per- and polyfluoroalkyl substances research
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