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双酚 A(TBBPA)及其替代品四溴双酚 S(TBBPS)和三溴双酚 A(TCBPA)对人体肝癌细胞代谢的潜在致肥胖作用。

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

机构信息

State Environmental Protection Key Laboratory of Environmental Pollution Health Risk Assessment, South China Institute of Environmental Sciences, Ministry of Ecology and Environment, Guangzhou 510655, China.

State Environmental Protection Key Laboratory of Environmental Pollution Health Risk Assessment, South China Institute of Environmental Sciences, Ministry of Ecology and Environment, Guangzhou 510655, China; School of Public Health, China Medical University, Liaoning 110122, China.

出版信息

Sci Total Environ. 2022 Aug 1;832:154847. doi: 10.1016/j.scitotenv.2022.154847. Epub 2022 Mar 28.

Abstract

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 μmol/L and 1 μmol/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 re-evaluation of the health risks associated with TBBPA and its alternatives TBBPS and TCBPA.

摘要

迄今为止,越来越多的研究表明四溴双酚 A(TBBPA)具有致肥胖作用。四溴双酚 S(TBBPS)和四氯双酚 A(TCBPA)是 TBBPA 的两种常见替代品,其环境分布经常被报道。然而,它们的毒性及其相关的潜在健康风险记录甚少。在此,我们采用非靶向代谢组学研究了 HepG2 细胞暴露于 TBBPA 及其替代品后的代谢紊乱情况。结果表明,在 HepG2 细胞中,浓度为 0.1 μmol/L 和 1 μmol/L 的 TBBPA、TBBPS 和 TCBPA 均未观察到细胞活力丧失。然而,多变量分析和代谢图谱显示,TBBPS 和 TCBPA 暴露后 HepG2 细胞中甘油磷脂和脂肪酸酰基水平出现显著紊乱。葡萄糖 1-磷酸和果糖 6-磷酸水平的明显升高可能是由于 PGM1/PGM2 和 GPI 基因表达的促进以及 UPG2 和 GFPT1/GFPT2 基因表达的抑制所导致的。我们的研究结果表明,TBBPS 和 TCBPA 比 TBBPA 更有可能破坏肝脏代谢平衡并潜在导致肝功能障碍。我们的研究对于重新评估 TBBPA 及其替代品 TBBPS 和 TCBPA 相关的健康风险具有重要意义。

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