4.7 Article

Potential obesogenic effects of TBBPA and its alternatives TBBPS and TCBPA revealed by metabolic perturbations in human hepatoma cells

Journal

SCIENCE OF THE TOTAL ENVIRONMENT
Volume 832, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.scitotenv.2022.154847

Keywords

Tetrabromobisphenol A; Brominated flame retardants; Metabolomics; Obesogens; Sugar metabolism

Funding

  1. National Natural Science Foundation of China [41931298, 21876059]
  2. Basic Research Foundation of National Commonwealth Research Institute [PM-zx703-202104-049]

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This study investigated the metabolic effects of tetrabromobisphenol A (TBBPA) and its alternatives on liver cells using metabolomics. The results revealed that exposure to TBBPS and TCBPA disrupted glycerophospholipid and fatty acyl levels and altered glucose and fructose metabolism pathways. The findings suggest that TBBPS and TCBPA may pose a higher risk to liver metabolic homeostasis and function compared to TBBPA.
To date, increasing numbers of studies have shown the obesogenic effects of tetrabromobisphenol A (TBBPA). Tetrabromobisphenol S (TBBPS) and tetrachlorobisphenol A (TCBPA) are two common alternatives to TBBPA, and their environmental distributions are frequently reported. However, their toxicity and the associated potential health risks are poorly documented. Herein, we performed untargeted metabolomics to study the metabolic perturbations in HepG2 cells exposed to TBBPA and its alternatives. Consequently, no loss of cellular viability was observed in HepG2 cells exposed to 0.1 mu mol/L and 1 mu mol/L TBBPA, TBBPS and TCBPA. However, multivariate analysis and metabolic profiles revealed significant perturbations in glycerophospholipid and fatty acyl levels in HepG2 cells exposure to TBBPS and TCBPA. The evident increases in the glucose 1-phosphate and fructose 6-phosphate levels in HepG2 cells were proposed to be induced by the promotion of PGM1/PGM2 and GPI gene expression and the suppression of UPG2 and GFPT1/GFPT2 gene expression. Our results suggest that TBBPS and TCBPA are more likely to disrupt liver metabolic homeostasis and potentially drive liver dysfunction than TBBPA. Our study is significant for the reevaluation of the health risks associated with TBBPA and its alternatives TBBPS and TCBPA.

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