Abstract

Triphenyl phosphate is a high production volume organophosphate flame retardant that has been detected in multiple environmental media at increasing concentrations. The environmental and health risks of triphenyl phosphate have drawn attention because of the multiplex toxicity of this chemical compound. However, few studies have paid close attention to the impacts of triphenyl phosphate on liver metabolism. We investigated hepatic histopathological, metabolomic and transcriptomic responses of zebrafish after exposure to 0.050 mg/L and 0.300 mg/L triphenyl phosphate for 7 days. Metabolomic analysis revealed significant changes in the contents of glucose, UDP-glucose, lactate, succinate, fumarate, choline, acetylcarnitine, and several fatty acids. Transcriptomic analysis revealed that related pathways, such as the glycosphingolipid biosynthesis, PPAR signaling pathway and fatty acid elongation, were significantly affected. These results suggest that triphenyl phosphate exposure markedly disturbs hepatic carbohydrate and lipid metabolism in zebrafish. Moreover, DNA replication, the cell cycle, and non-homologous end-joining and base excision repair were strongly affected, thus indicating that triphenyl phosphate hinders the DNA damage repair system in zebrafish liver cells. The present study provides a systematic analysis of the triphenyl phosphate-induced toxic effects in zebrafish liver and demonstrates that low concentrations of triphenyl phosphate affect normal metabolism and cell cycle.

Highlights

  • The metabolomic analysis of the toxic effects of TPhP in zebrafish liver was performed based on 1H nuclear magnetic resonance (NMR)

  • After we obtained the metabolomic profiles of different samples in the control and TPhP-treated (0.050 mg/L, 0.300 mg/L) groups, partial least squares-discriminant analysis (PLS-DA) analysis was performed for pattern recognition (Fig. 1,A)

  • The clear separation of samples from different treatment groups in the score plot of the PLS-DA model indicated that TPhP induced significant changes in zebrafish liver metabolomics

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Summary

Introduction

Alam et al have investigated the metabolic influences of tributyl phosphate (TBP) and TPhP in a nuclear magnetic resonance (NMR)-based metabolomics study of rat urine and have found that TPhP disturbs cellular energy metabolism and creatine synthesis in rats[26]. Zebrafish provide several experimental advantages, such as their low cost, ease of raising large numbers of animals, rapid liver development, and similar molecular and cellular processes to those of humans. They have been widely employed as a model organism in human disease research and in aquatic ecosystem health studies. Histopathological liver changes, blood glucose levels and blood lipid levels were investigated to provide a systematic understanding of adverse effects induced by TPhP in zebrafish

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