Alteration of sex hormone levels and steroidogenic pathway by several low molecular weight phthalates and their metabolites in male zebrafish (Danio rerio) and/or human adrenal cell (H295R) line

被引:57
作者
Sohn, Juhae [1 ]
Kim, Sujin [1 ]
Koschorreck, Jan [2 ]
Kho, Younglim [3 ]
Choi, Kyungho [1 ]
机构
[1] Seoul Natl Univ, Sch Publ Heath, Dept Environm Hlth Sci, Seoul 08826, South Korea
[2] Fed Environm Agcy Umweltbundesamt, D-06813 Dessau Rosslau, Germany
[3] Eulji Univ, Dept Hlth Environm & Safety, Songnam 13135, South Korea
基金
新加坡国家研究基金会;
关键词
Low molecular weight phthalates; Hydrolytic metabolites; Fish; Sex hormones; BUTYL BENZYL PHTHALATE; ENDOCRINE DISRUPTING CHEMICALS; DIISOBUTYL PHTHALATE; TESTOSTERONE PRODUCTION; SUBTROPICAL CITY; GENE-EXPRESSION; URBAN LAKES; EXPOSURE; ESTERS; RAT;
D O I
10.1016/j.jhazmat.2016.08.008
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Low molecular weight phthalates, such as diethyl phthalate (DEP), benzyl butyl phthalate (BBzP), or diisobutyl phthalate (DiBP), are suspected to disrupt endocrine system. However, their adverse effects on sex steroid hormones and underlying mechanisms are not well-documented. The aim of this study is to investigate the effects of major low molecular weight phthalates (LMWPs), i.e., DEP, BBzP, and DiBP, and their hydrolytic metabolites, on sex steroid hormone system, employing male zebrafish and/or a human adrenocortical carcinoma (H295R) cell. In male zebrafish, 14-day exposure to DEP, BBzP, or DiBP significantly decreased testosterone (T) concentrations. All test compounds significantly up-regulated cyp19a gene expression, and down-regulated star and 3 beta hsd genes in the male fish. In H295R cell, all test compounds except monoisobutyl phthalate (MiBP) reduced T concentrations and increased E2/T ratio. Gene expression changes in H295R cell, e.g., significant down-regulation of StAR gene and up-regulation of CYP19A gene, supported depressed synthesis of sex hormones in the adrenal cell. Our results show that not only DEP, BBzP, and DiBP, but also their hydrolytic metabolites disrupt sex hormone balances through modulating key steroidogenic genes in the human adrenal cells and in zebrafish. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:45 / 54
页数:10
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