Guangdong Key Laboratory of Environmental Pollution and Health, School of Environment, Jinan University, Guangzhou, 510632, China.
Key Laboratory for City Cluster Environmental Safety and Green Development of the Ministry of Education, Institute of Environmental and Ecological Engineering, Guangdong University of Technology, Guangzhou, 510006, China.
Environ Pollut. 2021 Dec 15;291:118106. doi: 10.1016/j.envpol.2021.118106. Epub 2021 Sep 4.
Phthalates are plasticizers in various products and regarded as endocrine disruptors due to their anti-androgen effects. Environmental occurrence and toxicities of parent phthalates have been widely reported, while the current state of knowledge on their metabolites is rarely summarized. Based on the available literature, the present review mainly aims to 1) characterize the potential metabolites of phthalates (mPAEs) using the pharmacokinetics evidences acquired via animal or human models; 2) examine the molecular and cellular mechanism involved in toxicity for mPAEs; 3) investigate the exposure levels of mPAEs in different human specimens (e.g., urine, blood, seminal fluid, breast milk, amniotic fluid and others) across the globe; 4) discuss the models and related parameters for phthalate exposure assessment. We suggest there is subtle difference in toxic mechanisms for mPAEs compared to their parent phthalates due to their alternative chemical structures. Human monitoring studies performed in Asia, America and Europe have provided the population exposure baseline levels for typical phthalates in different regions. Urine is the preferred matrix than other specimens for phthalate exposure study. Among ten urinary mPAEs, the largest proportions of di-(2-ethylhexyl) phthalate (DEHP) metabolites (40%), monoethyl phthalate (mEP) (43%) and DEHP metabolites/mEP (both 29%) were observed in Asia, America and Europe respectively, and mono-5-carboxy-2-ethypentyl phthalate was the most abundant compounds among DEHP metabolites. Daily intakes of phthalates can be accurately calculated via urinary mPAEs if the proper exposure parameters were determined. Further work should focus on combining epidemiological and biological evidences to establish links between phthalates exposure and biological phenotypes. More accurate molar fractions (F) of the urinary excreted monoester related to the ingested diesters should be collected in epidemiological or pharmacokinetic studies for different population.
邻苯二甲酸酯是各种产品中的增塑剂,由于其抗雄激素作用,被认为是内分泌干扰物。已广泛报道了原邻苯二甲酸酯的环境发生和毒性,而其代谢物的现有知识状况很少得到总结。基于现有文献,本综述主要旨在:1)利用通过动物或人体模型获得的药代动力学证据,描述邻苯二甲酸酯的潜在代谢物(mPAEs);2)研究 mPAEs 毒性涉及的分子和细胞机制;3)在全球范围内调查不同人体标本(例如尿液、血液、精液、母乳、羊水等)中 mPAEs 的暴露水平;4)讨论评估邻苯二甲酸酯暴露的模型和相关参数。我们认为,由于其替代化学结构,mPAEs 的毒性机制与它们的母体邻苯二甲酸酯略有不同。亚洲、美洲和欧洲进行的人体监测研究为不同地区的典型邻苯二甲酸酯提供了人群暴露基线水平。尿液是进行邻苯二甲酸酯暴露研究的首选基质,而其他标本则次之。在十种尿液 mPAEs 中,DEHP 代谢物(40%)、mEP(43%)和 DEHP 代谢物/mEP(均为 29%)在亚洲、美洲和欧洲的比例最大,而 DEHP 代谢物中最丰富的化合物是单-5-羧基-2-乙基戊基邻苯二甲酸酯。如果确定了适当的暴露参数,则可以通过尿液 mPAEs 准确计算出邻苯二甲酸酯的每日摄入量。进一步的工作应侧重于结合流行病学和生物学证据,在不同人群中建立邻苯二甲酸酯暴露与生物学表型之间的联系。在流行病学或药代动力学研究中,应针对不同人群收集更准确的与摄入的二酯相关的单酯尿液排泄的摩尔分数(F)。