首页> 美国卫生研究院文献>International Journal of Biological Sciences >Endosulfan-Induced Biomarkers in Japanese Rice Fish (Oryzias latipes) Analyzed by SELDI-TOF-MS
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Endosulfan-Induced Biomarkers in Japanese Rice Fish (Oryzias latipes) Analyzed by SELDI-TOF-MS

机译:SELDI-TOF-MS分析日本稻鱼(Oryzias latipes)中硫丹诱导的生物标志物

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摘要

The objective of this study was to find and validate estrogen-related biomarkers from plasma proteins in Oryzias latipes after exposure to an estrogen disrupting compound, α-endosulfan. The acute toxicity of α-endosulfan on O. latipes after 96 h of exposure was 13.72, 16.18, and 22.18 μg L-1 for the LC10, LC20, and LC50 values, respectively. To confirm estrogenic disturbance by α-endosulfan, the expression level of vitellogenin in the liver of male fishes was measured at the LC10 value, and it was found to be significantly different from the reference group, confirming the estrogenic effect of endosulfan in this concentration range. Proteinchip® array techniques using a weak cation exchange (CM10) and a strong anion exchange proteinchip (Q10) in conjunction with surface-enhanced laser desorption/ionization time of flight mass spectrometry (SELDI-TOF-MS) were used to determine plasma proteins of O. latipes differently expressed in response to endosulfan exposure at LC10 and LC20 concentrations. Analysis of protein profiling of the male fish exposed to α-endosulfan detected 48 significantly different protein peaks and the proteins at m/z 2819, 8462, 8860, and 9462 were significantly different (p<0.05). The protein peaks at m/z 2819, 8860, and 9462 were up-regulated and the peak at m/z 8462 was down-regulated. Therefore, these four differentially expressed proteins could be used as biomarkers to rapidly determine a possible risk of endosulfan on aquatic ecosystems, although these are not necessarily produced as a result of endocrine disruption.
机译:这项研究的目的是在暴露于雌激素破坏性化合物α-硫丹后,从稻米中的血浆蛋白中发现并验证与雌激素相关的生物标记。暴露96 h后,α-硫丹对油菜的急性毒性分别为LC10,LC20和LC50值分别为13.72、16.18和22.18μgL -1 。为了确认α-硫丹对雌激素的干扰,在LC10值下测定雄鱼肝脏中卵黄蛋白原的表达水平,发现与参考组有显着差异,从而证实了该浓度范围内硫丹的雌激素作用。 。使用微弱阳离子交换(CM10)和强阴离子交换蛋白质芯片(Q10)结合表面增强的激光解吸/电离飞行时间质谱(SELDI-TOF-MS)的Proteinchip®阵列技术确定血浆蛋白O. latipes在LC10和LC20浓度下响应硫丹暴露而表达不同。对暴露于α-硫丹的雄鱼的蛋白质谱分析分析发现了48个显着不同的蛋白质峰,并且m / z 2819、8462、8860和9462处的蛋白质存在显着差异(p <0.05)。 m / z 2819、8860和9462处的蛋白质峰上调,而m / z 8462处的蛋白质峰下调。因此,这四种差异表达的蛋白质可以用作生物标记物,以快速确定水生生态系统中硫丹的可能风险,尽管不一定由于内分泌干扰而产生这些硫丹。

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