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Tissue-specific induction of EROD activity and CYP1A protein in Sparus aurata exposed to B(α)P and TCDD

机译:暴露于B(α)P和TCDD的灵芝中EROD活性和CYP1A蛋白的组织特异性诱导

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The purpose of this study was to compare xenobiotic CYP1A induction in liver, gills, and excretory kidney of gilthead seabream, Sparus aurata. Fishes were exposed via water for 20 days to different concentrations of benzo(α)pyrene (B(α)P) or 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). CYP1A was measured at the enzyme activity level as 7-ethoxyresorufin-O-deethylase (EROD) activity, and at the protein level by means of ELISA. The liver displayed the highest absolute levels of EROD activity, both under non-exposed and exposed conditions. Organ- or inducer-related differences in the time course of CYP1A induction were moderate; however, the magnitude of the induction response varied between the organs and between B(α)P and TCDD. In the case of TCDD, liver, and kidney yielded a comparable induction response, whereas in the case of B(α)P, the kidney showed a substantially higher maximum induction factor than the liver. In the gills, the two xenobiotics resulted in similar maximum induction factors. In B(α)P-exposed seabream, EROD activities and CYP1A protein levels showed a good correlation in all three organs, whereas with TCDD as inducer the correlation was poor, what was mainly due to a decrease of EROD activities at the higher concentrations of TCDD, while CYP1A protein levels showed no concomitant decline. Overall, the study revealed both similarities and differences in the time-, concentration-, and inducer-dependent CYP1A responses of the three target organs, liver, kidney, and gills. Although, the findings of this study principally confirm the notion of the liver as the major metabolic organ in fish, they also provide evidence for substantial metabolic potential in gills and particularly in the kidney.
机译:本研究的目的是比较银头鲷(Sparus aurata)在肝脏,腮和排泄肾脏中的异源CYP1A诱导作用。鱼类通过水暴露于不同浓度的苯并(α)((B(α)P)或2,3,7,8-四氯二苯并-对二恶英(TCDD)中达20天。 CYP1A的酶活性水平为7-乙氧基间苯二酚-O-脱乙基酶(EROD)活性,蛋白水平为ELISA法。在未暴露和暴露条件下,肝脏均显示出最高的EROD活性绝对水平。 CYP1A诱导时间的器官或诱导物相关差异中等。然而,诱导反应的幅度在器官之间以及B(α)P和TCDD之间变化。在TCDD的情况下,肝脏和肾脏产生的诱导反应相当,而在B(α)P的情况下,肾脏显示的最大诱导因子明显高于肝脏。在the中,两种异生素产生相似的最大诱导因子。在暴露于B(α)P的鲷鱼中,EROD活性和CYP1A蛋白水平在所有三个器官中均显示出良好的相关性,而以TCDD为诱导剂的相关性较弱,这主要是由于较高浓度的EROD活性降低了。 TCDD,而CYP1A蛋白水平未见伴随下降。总的来说,该研究揭示了三个靶器官(肝,肾和腮)在时间,浓度和诱导剂依赖性CYP1A反应中的相似性和差异。尽管这项研究的发现主要证实了肝脏是鱼类主要的代谢器官的概念,但它们也提供了g,特别是肾脏中大量代谢潜能的证据。

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