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首页> 外文期刊>Journal of Environmental Sciences >Assessing the anti-estrogenic activity of sodium pentachlorophenol in primary cultures of juvenile goldfish (Carassius auratus) hepatocytes using vitellogenin as a biomarker
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Assessing the anti-estrogenic activity of sodium pentachlorophenol in primary cultures of juvenile goldfish (Carassius auratus) hepatocytes using vitellogenin as a biomarker

机译:使用卵黄蛋白原作为生物标记物评估少年金鱼((鱼)肝细胞原代培养物中五氯酚钠的抗雌激素活性

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摘要

Both pentachlorophenol and 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) had been studied widely because of their probable anti-estrogenic activity. Sodium pentachlorophenol (PCP-Na), as a industrial product used in many fields, usually contains a trace of TCDD. The aim of this study was to assess the anti-estrogenic effect of PCP-Na in juvenile goldfish (Carassius auraius) hepatocyte cultures using vitellogenin (VTG) as the biomarker. The ID_(50) of PCP-Na was investigated and then a series of concentrations (0.001-0.5 mu g/ml) of PCP-Na were evaluated to estimate the anti-estrogenic activity. Results showed that PCP-Na was cytotoxic for hepatocytes even at very low concentration <1.21 mu g/ml, and it could not induce VTG at any concentrations tested. Since it failed to stimulate VTG production, the possibility of its anti-estrogenic effect was tested, and a well-known anti-estrogenic compound-tamoxifen was used as positive control. PCP-Na caused a reduction in VTG synthesis in juvenile goldfish (Carassius auratus) hepatocytes at concentrations >0.1 mu g/ml when co-exposure with 1 mu g/ml 17p-estradiol (E2), making its anti-estrogenic activity approximately as potent as tamoxifen. Our results indicate that PCP-Na can act as negative modulators of estrogenic function in juvenile goldfish (Carassius auratus) hepatocytes.
机译:五氯苯酚和2,3,7,8-四氯二苯并-对-二恶英(TCDD)均已被广泛研究,因为它们可能具有抗雌激素活性。五氯苯酚钠(PCP-Na)作为许多领域的工业产品,通常都含有微量的TCDD。这项研究的目的是评估使用卵黄蛋白原(VTG)作为生物标记物,PCP-Na在幼稚金鱼(Carassius auraius)肝细胞培养物中的抗雌激素作用。研究PCP-Na的ID_(50),然后评估一系列浓度(0.001-0.5μg/ ml)的PCP-Na以估计抗雌激素活性。结果表明,即使在浓度<1.21μg / ml的极低浓度下,PCP-Na对肝细胞也具有细胞毒性,并且在任何测试浓度下均不能诱导VTG。由于它不能刺激VTG的产生,因此测试了其抗雌激素作用的可能性,并将众所周知的抗雌激素化合物他莫昔芬用作阳性对照。当与1μg/ ml的17p-雌二醇(E2)共同暴露时,PCP-Na导致浓度> 0.1μg/ ml的幼年金鱼(Car鱼)肝细胞中VTG合成减少,使其抗雌激素活性约为如他莫昔芬有效。我们的结果表明,PCP-Na可以在幼年金鱼(Carassius auratus)肝细胞中充当雌激素功能的负调节剂。

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