Developmental toxicity of endocrine disruptors in early life stages of zebrafish, a genetic and embryogenesis study

被引:52
|
作者
Santos, Dercia [1 ]
Matos, Manuela [1 ,2 ]
Coimbra, Ana M. [1 ,3 ]
机构
[1] UTAD, Life Sci & Environm Sch, P-5000801 Quinta De Prados, Vila Real, Portugal
[2] UTAD, IBB CGB, P-5000801 Quinta De Prados, Vila Real, Portugal
[3] UTAD, Ctr Res & Technol Agroenvironm & Biol Sci CITAB, P-5000801 Quinta De Prados, Vila Real, Portugal
关键词
17; alpha-Ethinylestradiol; Genistein; Fadrozole; Embryo-larval development; Gene expression; Zebrafish; MINNOW PIMEPHALES-PROMELAS; BRAIN AROMATASE-ACTIVITY; ESTROGEN-RECEPTOR GENES; MEDAKA ORYZIAS-LATIPES; C-JUN PROTOONCOGENE; DANIO-RERIO; ANDROGEN-RECEPTOR; BISPHENOL-A; MOLECULAR CHARACTERIZATION; ENVIRONMENTAL ESTROGENS;
D O I
10.1016/j.ntt.2014.08.002
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Endocrine disrupting compounds (EDCs) are capable of interfering with the endocrine system and are increasingly widespread in the aquatic environments. In the present study, zebrafish (Danio retro) embryos and larvae were used to assess how EDCs may interfere with embryogenesis. Therefore, zebrafish embryos were exposed to 17 alpha-ethinylestradiol (EE2: 0.4,2,4 and 20 ng/L),genistein (Gen: 2,20, 200 and 2000 ng/L) and fadrozole (Fad: 2, 10, 50 and 250 mu g/L) between 2 and 144 h post-fertilization (hpf). Somite development, heartbeat, malformations, mortality and hatching rates were evaluated. In parallel, the expression patterns of hormone receptors (esrl, esr2a, esr2b and ar) and apoptotic pathways related genes (p53 and c-jun) were determined using quantitative real-time PCR. Results showed that EE2, Gen and Fad caused a higher mortality and also malformations in larvae compared with control. A significant toxic effect was observed in the heartbeat rate, at 144 hpf, in larvae exposed to EE2 and Fad. QPCR revealed alterations in the expression levels of all the evaluated genes, at different time points. esrl and c-jun genes were upregulated by EE2 and Gen exposure while the expression of esr2a, esr2b and or genes was downregulated. Fad exposure decreased esrl, p53 and c-jun expression levels. This study shows a toxic effect of EE2, Gen and Fad to vertebrate embryogenesis and a relation between hormones action and apoptosis pathways. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:18 / 25
页数:8
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