首页> 外文期刊>Journal of applied toxicology >Developing in vitro reporter gene assays to assess the hormone receptor activities of chemicals frequently detected in drinking water
【24h】

Developing in vitro reporter gene assays to assess the hormone receptor activities of chemicals frequently detected in drinking water

机译:开发体外报告基因测定法以评估饮用水中经常检测到的化学物质的激素受体活性

获取原文
获取原文并翻译 | 示例
           

摘要

The present study intended to develop receptor-mediated luciferase reporter gene assays to evaluate and compare the estrogen receptor (ER), androgen receptor (AR) and thyroid hormone receptor (TR) activities of target chemicals. Di-2-ethylhexyl-phthalate (DEHP), chlorpyrifos (CPF), 2,4-dichlorophenoxyacetic acid (2,4-D) and bisphenol A (BPA) are some of the most common contaminants in drinking water and are frequently detected in China and worldwide. The chemicals were tested at concentrations of 0.1, 1, 10 and 100 times their maximum contaminant level in drinking water. The results showed that BPA possessed various activities on ER, AR and TR. DEHP and CPF could suppress 17β-estradiol or testosterone activity with different potencies, and DEHP possessed weaker anti-thyroid hormone activity. 2,4-D showed no agonist or antagonist activity against these hormone receptors, but it significantly enhanced the activity of testosterone through AR. Furthermore, the mixture of DEHP and CPF exhibited stronger ER and AR antagonist activities than each single component alone, but their combined effects were less than the expected effects based on the additive model. These results implied that the transcription activation mediated by hormone receptors was the potential endocrine-disrupting mechanism of the test chemicals. Our study also provided useful tools for evaluation of their endocrine disrupting activity.
机译:本研究旨在开发受体介导的萤光素酶报告基因测定法,以评估和比较目标化学物质的雌激素受体(ER),雄激素受体(AR)和甲状腺激素受体(TR)活性。邻苯二甲酸二-2-乙基己基酯(DEHP),毒死rif(CPF),2,4-二氯苯氧基乙酸(2,4-D)和双酚A(BPA)是饮用水中最常见的一些污染物,通常在饮用水中被检测到。中国及全球。所测试的化学品的浓度为饮用水中最大污染物含量的0.1、1、10和100倍。结果表明,双酚A在ER,AR和TR上具有多种活性。 DEHP和CPF可以不同程度地抑制17β-雌二醇或睾丸激素的活性,而DEHP的抗甲状腺激素活性较弱。 2,4-D对这些激素受体没有激动剂或拮抗剂活性,但通过AR显着增强了睾丸激素的活性。此外,DEHP和CPF的混合物显示出比单独的每种单一组分更强的ER和AR拮抗剂活性,但它们的组合作用小于基于加性模型的预期作用。这些结果暗示激素受体介导的转录激活是受试化学物质潜在的内分泌干扰机制。我们的研究还为评估其内分泌干扰活性提供了有用的工具。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号