Effects of Mixed Exposure to Bisphenol F (BPF) and Perfluorooctane Sulfonic Acid (PFOS) on Hepatotoxicity and Lipid Metabolism in Zebrafish

Background: Chemicals such as bisphenols and perfluorinated compounds exist mixed in surrounding water, but the toxicity of such mixtures is not well known.Objectives: This study investigated the effects, both individually and in mixture, of bisphenol F (BPF) and perfluorooctane sulfonic acid (PFOS) on the liver toxicity and lipid metabolism of zebrafish.Methods: Zebrafish embryos were exposed to single and binary mixture of BPF (0.03~300 g/L) and PFOS (0.01~100 g/L) for 96 hours.Survival and growth endpoints were observed daily.To investigate liver toxicity, the activities of alanine aminotransferase (ALT) and aspartate aminotransferase (AST) and the transcription of genes related to the peroxisome proliferator-activated receptor (PPAR), endoplasmic reticulum stress (ERS), and apoptosis were all evaluated.To explain the toxic mechanism of increased hepatotoxicity that occurs when BPF and PFOS are mixed, changes in the expression of the cytochrome P450 3a65 (cyp3a65) gene were measured.Results: A significant decrease in body length was observed in zebrafish larvae exposed to 30 and 300 g/ L of BPF, 100 g/L of PFOS, and the mixture.The activities of ALT were significantly increased in larvae exposed to BPF.Enzyme activities were well supported by the regulation of ppara, chop, eif2a, baxa, bcl2a, and casp genes.When zebrafish were co-exposed to BPF and PFOS, the expression of the cyp3a65 gene was significantly reduced, while the levels of ALT and AST were increased.These results suggest that PFOS could increase the hepatotoxicity of BPF that depends on the CYP metabolism for its elimination. Conclusions:The results of this study indicated that BPF can induce hepatotoxicity and interfere with lipid metabolism, and PFOS increases the hepatotoxicity of BPF by inhibiting CYP metabolism.Combined contamination of BPF and PFOS may be a potentially hazardous factor, and further investigation is needed for risk assessment.

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Publication Details

Journal
Korean Journal of Environmental Health Sciences
Published
2025-08-29
DOI
https://doi.org/10.5668/jehs.2025.51.4.230
Primary Topic
Per- and polyfluoroalkyl substances research
Type
article
Field-Weighted Citation Impact
0.00

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article

Effects of Mixed Exposure to Bisphenol F (BPF) and Perfluorooctane Sulfonic Acid (PFOS) on Hepatotoxicity and Lipid Metabolism in Zebrafish

Da Yeong Lee, Kyunghee Ji
Korean Journal of Environmental Health Sciences
Per- and polyfluoroalkyl substances research
article

Effects of Mixed Exposure to Bisphenol F (BPF) and Perfluorooctane Sulfonic Acid (PFOS) on Hepatotoxicity and Lipid Metabolism in Zebrafish

Da Yeong Lee, Kyunghee Ji
article en

Abstract

Background: Chemicals such as bisphenols and perfluorinated compounds exist mixed in surrounding water, but the toxicity of such mixtures is not well known.Objectives: This study investigated the effects, both individually and in mixture, of bisphenol F (BPF) and perfluorooctane sulfonic acid (PFOS) on the liver toxicity and lipid metabolism of zebrafish.Methods: Zebrafish embryos were exposed to single and binary mixture of BPF (0.03~300 g/L) and PFOS (0.01~100 g/L) for 96 hours.Survival and growth endpoints were observed daily.To investigate liver toxicity, the activities of alanine aminotransferase (ALT) and aspartate aminotransferase (AST) and the transcription of genes related to the peroxisome proliferator-activated receptor (PPAR), endoplasmic reticulum stress (ERS), and apoptosis were all evaluated.To explain the toxic mechanism of increased hepatotoxicity that occurs when BPF and PFOS are mixed, changes in the expression of the cytochrome P450 3a65 (cyp3a65) gene were measured.Results: A significant decrease in body length was observed in zebrafish larvae exposed to 30 and 300 g/ L of BPF, 100 g/L of PFOS, and the mixture.The activities of ALT were significantly increased in larvae exposed to BPF.Enzyme activities were well supported by the regulation of ppara, chop, eif2a, baxa, bcl2a, and casp genes.When zebrafish were co-exposed to BPF and PFOS, the expression of the cyp3a65 gene was significantly reduced, while the levels of ALT and AST were increased.These results suggest that PFOS could increase the hepatotoxicity of BPF that depends on the CYP metabolism for its elimination. Conclusions:The results of this study indicated that BPF can induce hepatotoxicity and interfere with lipid metabolism, and PFOS increases the hepatotoxicity of BPF by inhibiting CYP metabolism.Combined contamination of BPF and PFOS may be a potentially hazardous factor, and further investigation is needed for risk assessment.

Korean Journal of Environmental Health SciencesVol. 51(4)
Yong In University (KR)
Ministry of Environment
Openalex Percentile: Top 81%
Per- and polyfluoroalkyl substances research
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Effects of Mixed Exposure to Bisphenol F (BPF) and Perfluorooctane Sulfonic Acid (PFOS) on Hepatotoxicity and Lipid Metabolism in Zebrafish — Da Yeong Lee, Kyunghee Ji · Korean Journal of Environmental Health Sciences (2025) | TGRS Research Map | TGRS