Zhu Li-Zhen, Qi Su-Zhen, Cao Fang-Jie, Mu Xi-Yan, Yang Yang, Wang Chengju
College of Sciences, China Agricultural University, Beijing, People's Republic of China.
College of Sciences, China Agricultural University, Beijing, People's Republic of China; Institute of Apicultural Research, Chinese Academy of Agricultural Sciences, People's Republic of China.
Aquat Toxicol. 2017 Feb;183:76-84. doi: 10.1016/j.aquatox.2016.12.011. Epub 2016 Dec 12.
The herbicide Quizalofop-P-ethyl (QpE) exerts toxic effects in fish, but limited information is currently available on its effects on the endocrine system. In the current study, adult zebrafish (Danio rerio) were exposed to different concentrations (0, 2, 20, 200μg/L) of QpE for 30days. In males, QpE exposure significantly increased plasma estradiol (E2) and vitellogenin (VTG) levels, concomitant with up-regulation of hepatic esr1 and vtg gene expression. In females, plasma sex hormone levels and VTG concentrations were not altered significantly, but an increased expression of hepatic esr1 in addition to decreased expression of hepatic vtg, esr2a and esr2b was observed. Marked histological lesions were also observed in the gonads of both males and females. Moreover, QpE exposure significantly increased transcriptional profiles of some genes in the HPG axis and liver in males, while the majority of these genes were down-regulated in females. Docking studies showed QpE forming stable interactions with the ligand-binding domain (LBD) of zebrafish ESR1 and ESR2a, suggesting QpE may bind to estrogen receptors (ESRs). This study for the first time reveals QpE as an endocrine-disrupting chemical (EDC) disrupting the zebrafish endocrine system in a sex-specific manner, whereby it increases estrogen axis activity in males and slightly decreases estrogen axis activity in females, which may be accounted for by QpE regulating steroidogenesis and/or activating ESR(s).
除草剂精喹禾灵乙酯(QpE)对鱼类具有毒性作用,但目前关于其对内分泌系统影响的信息有限。在本研究中,成年斑马鱼(Danio rerio)暴露于不同浓度(0、2、20、200μg/L)的QpE中30天。在雄性斑马鱼中,QpE暴露显著提高了血浆雌二醇(E2)和卵黄蛋白原(VTG)水平,同时伴随着肝脏esr1和vtg基因表达的上调。在雌性斑马鱼中,血浆性激素水平和VTG浓度没有显著变化,但观察到肝脏esr1表达增加,同时肝脏vtg、esr2a和esr2b表达减少。在雄性和雌性斑马鱼的性腺中也观察到明显的组织学损伤。此外,QpE暴露显著增加了雄性斑马鱼下丘脑-垂体-性腺(HPG)轴和肝脏中一些基因的转录谱,而在雌性斑马鱼中,这些基因中的大多数被下调。对接研究表明,QpE与斑马鱼ESR1和ESR2a的配体结合域(LBD)形成稳定的相互作用,表明QpE可能与雌激素受体(ESR)结合。本研究首次揭示QpE是一种内分泌干扰化学物质(EDC),以性别特异性方式扰乱斑马鱼内分泌系统,从而增加雄性斑马鱼的雌激素轴活性,略微降低雌性斑马鱼的雌激素轴活性,这可能是由于QpE调节类固醇生成和/或激活雌激素受体所致。