Metabolomics Laboratory, College of Pharmacy, Korea University, Sejong City 30019, Republic of Korea.
Department of Preventive Medicine, College of Medicine, Ewha Womans University, Seoul 07985, Republic of Korea.
Toxicol Sci. 2017 Dec 1;160(2):371-385. doi: 10.1093/toxsci/kfx189.
Health risks associated with bisphenol A (BPA) exposure are controversially highlighted by numerous studies. High-resolution metabolomics (HRM) can confirm these proposed associations and may provide a mechanistic insight into the connections between BPA exposure and metabolic perturbations. This study was aimed to identify the changes in metabolomics profile due to BPA exposure in urine and serum samples collected from female and male children (n = 18) aged 7-9. Urine was measured for BPA concentration, and the children were subsequently classified into high and low BPA groups. HRM, coupled with Liquid chromatography-mass spectrometry/MS, followed by multivariate statistical analysis using MetaboAnalyst 3.0, were performed on urine to discriminate metabolic profiles between high and low BPA children as well as males and females, followed by further validation of our findings in serum samples obtained from same population. Metabolic pathway analysis showed that biosynthesis of steroid hormones and 7 other pathways-amino acid and nucleotide biosynthesis, phenylalanine metabolism, tryptophan metabolism, tyrosine metabolism, lysine degradation, pyruvate metabolism, and arginine biosynthesis-were affected in high BPA children. Elevated levels of metabolites associated with these pathways in urine and serum were mainly observed in female children, while these changes were negligible in male children. Our results suggest that the steroidogenesis pathway and amino acid metabolism are the main targets of perturbation by BPA in preadolescent girls.
与双酚 A(BPA)暴露相关的健康风险受到许多研究的争议性强调。高分辨率代谢组学(HRM)可以证实这些拟议的关联,并可能为 BPA 暴露与代谢紊乱之间的联系提供机制上的见解。本研究旨在确定 HRM 联合液相色谱-质谱/质谱(LC-MS/MS),并使用 MetaboAnalyst 3.0 进行多变量统计分析,从尿液和血清样本中识别出由于 BPA 暴露而导致的代谢组学特征的变化,这些样本来自年龄为 7-9 岁的女性和男性儿童(n = 18)。测量尿液中的 BPA 浓度,然后根据 BPA 浓度将儿童分为高 BPA 组和低 BPA 组。在尿液中区分高 BPA 儿童和低 BPA 儿童以及男性和女性的代谢特征,随后在来自同一人群的血清样本中进一步验证我们的发现,使用代谢组学分析,然后使用 MetaboAnalyst 3.0 进行多变量统计分析。代谢途径分析表明,生物合成甾体激素和 7 种其他途径-氨基酸和核苷酸生物合成、苯丙氨酸代谢、色氨酸代谢、酪氨酸代谢、赖氨酸降解、丙酮酸代谢和精氨酸生物合成-在高 BPA 儿童中受到影响。在尿液和血清中与这些途径相关的代谢物水平升高主要发生在女性儿童中,而在男性儿童中这些变化可以忽略不计。我们的结果表明,甾体生物合成途径和氨基酸代谢是 BPA 对青春期前女孩产生干扰的主要靶标。