| Literature DB >> 26741556 |
Thiago Scremin Boscolo Pereira1, Camila Nomura Pereira Boscolo1, Andreia Arantes Felício2, Sergio Ricardo Batlouni3, Daniel Schlenk4, Eduardo Alves de Almeida5.
Abstract
Some endocrine disrupting chemicals (EDCs) can alter the estrogenic activities of the organism by directly interacting with estrogen receptors (ER) or indirectly through the hypothalamus-pituitary-gonadal axis. Recent studies in male Nile tilapia (Oreochromis niloticus) indicated that diuron may have anti-androgenic activity augmented by biotransformation. In this study, the effects of diuron and three of its metabolites were evaluated in female tilapia. Sexually mature female fish were exposed for 25 days to diuron, as well as to its metabolites 3,4-dichloroaniline (DCA), 3,4-dichlorophenylurea (DCPU) and 3,4-dichlorophenyl-N-methylurea (DCPMU), at concentrations of 100 ng/L. Diuron metabolites caused increases in E2 plasma levels, gonadosomatic indices and in the percentage of final vitellogenic oocytes. Moreover, diuron and its metabolites caused a decrease in germinative cells. Significant differences in plasma concentrations of the estrogen precursor and gonadal regulator17α-hydroxyprogesterone (17α-OHP) were not observed. These results show that diuron metabolites had estrogenic effects potentially mediated through enhanced estradiol biosynthesis and accelerated the ovarian development of O. niloticus females.Entities:
Keywords: Diuron; Diuron metabolites; Endocrine disrupting chemicals; Gametogenesis; Nile tilapia
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Year: 2015 PMID: 26741556 DOI: 10.1016/j.chemosphere.2015.12.073
Source DB: PubMed Journal: Chemosphere ISSN: 0045-6535 Impact factor: 7.086