首页> 外文期刊>Environmental toxicology and chemistry >ETHOXYRESORUFIN-O-DEETHYLASE INDUCTION POTENCY OF POLYCHLORINATED DIPHENYL ETHERS IN H4IIE RAT HEPATOMA CELLS
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ETHOXYRESORUFIN-O-DEETHYLASE INDUCTION POTENCY OF POLYCHLORINATED DIPHENYL ETHERS IN H4IIE RAT HEPATOMA CELLS

机译:H4IIE大鼠肝癌细胞中多氯联苯醚的乙氧基间苯二酚-O-脱乙基酶诱导潜能

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Polychlorinated diphenyl ethers (PCDEs) are structurally similar to polychlorinated biphenyls (PCBs), and some PCDE congeners have been reported to cause toxic responses similar to those caused by some of the non-ortho-substituted PCBs, which are mediated by the aryl hydrocarbon receptor (AhR). Twenty-nine PCDEs were tested for their potency as AhR agonists relative to 2,3,7,8-tetrachlorodibenzo-p-dioxin (2,3,7,8-TCDD) by measuring their ability to induce the cytochrome P-450 1A1-associated enzyme activity, ethoxyresorufin-0-deethylase (EROD), in the H4IIE rat hepatoma cell bioassay. All PCDE congeners tested were found to be inactive as EROD inducers except for PCDE 156, which was a weak EROD inducer with a 2,3,7,8-TCDD equivalency factor of about 1.2 X 10~(-5). During this study we determined that small amounts of polychlorinated dibenzofurans (PCDFs) that occurred as impurities in the PCDE preparations were the cause of the apparent EROD induction initially measured in our experiments. Once the PCDF impurities were removed by purification on florisll, little or no activity could be attributed to the PCDEs.
机译:多氯联苯醚(PCDE)在结构上与多氯联苯(PCB)类似,并且据报道,某些PCDE同系物会产生类似于由芳烃受体介导的某些非邻位取代PCB引起的毒性反应(AhR)。测试了29种PCDE作为AhR激动剂相对于2,3,7,8-四氯二苯并-p-二恶英(2,3,7,8-TCDD)的效能,方法是测量它们诱导细胞色素P-450 1A1的能力。 H4IIE大鼠肝癌细胞生物测定中,β-相关的酶活性为乙氧基试卤灵-0-脱乙基酶(EROD)。发现所有测试的PCDE同系物均不作为EROD诱导剂起作用,但PCDE 156除外,它是弱EROD诱导剂,其2,3,7,8-TCDD当量系数约为1.2 X 10〜(-5)。在这项研究中,我们确定了在PCDE制剂中以杂质形式出现的少量多氯二苯并呋喃(PCDF)是在我们的实验中最初测量到的明显EROD诱导的原因。一旦通过弗洛里斯尔纯化除去了PCDF杂质,几乎没有或没有活性可归因于PCDE。

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