Bisphenol A and its analogs: Do their metabolites have endocrine activity?

被引:163
作者
Skledar, Darja Gramec [1 ]
Masic, Lucija Peterlin [1 ]
机构
[1] Univ Ljubljana, Fac Pharm, Ljubljana, Slovenia
关键词
Bisphenol A; BPA analogs; Hormone disruptors; Oxidative metabolism; Glucuronidation; Endocrine toxicity; RAT UTEROTROPHIC ASSAY; IN-VITRO; TETRABROMOBISPHENOL-A; FLAME-RETARDANT; UNITED-STATES; ESTROGENIC ACTIVITY; STRUCTURAL ANALOGS; UDP-GLUCURONOSYLTRANSFERASE; HUMAN URINE; LIVER;
D O I
10.1016/j.etap.2016.09.014
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Structural analogs of bisphenol A are commonly used as its alternatives in industrial and commercial applications. Nevertheless, the question arises whether the use of other bisphenols is justified as replacements for bisphenol A in mass production of plastic materials. To evaluate the influence of metabolic reactions on endocrine activities of bisphenols, we conducted a systematic review of the literature. Knowledge about the metabolic pathways and enzymes involved in metabolic biotransformations is essential for understanding and predicting mechanisms of toxicity. Bisphenols are metabolized predominantly by the glucuronidation reaction, which is considered their most important detoxification pathway, as based on current knowledge, glucuronides do not have activity on endocrine receptors. In contrast, several oxidative metabolites of bisphenols with enhanced endocrine activities are presented, and these findings indicate that oxidative metabolites of bisphenols can still have endocrine activities in humans. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:182 / 199
页数:18
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