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作为孕烷X受体(PXR)激活剂的工业用五溴二苯醚和六溴环十二烷

Technical pentabromodiphenyl ether and hexabromocyclododecane as activators of the pregnane-X-receptor (PXR).

作者信息

Fery Yvonne, Buschauer Inga, Salzig Christian, Lang Patrick, Schrenk Dieter

机构信息

Food Chemistry and Toxicology, University of Kaiserslautern, Erwin-Schroedinger-Strasse 52, D-67663 Kaiserslautern, Germany.

出版信息

Toxicology. 2009 Oct 1;264(1-2):45-51. doi: 10.1016/j.tox.2009.07.009. Epub 2009 Jul 23.

Abstract

Technical pentabrominated diphenyl ether (pentaBDE mix) is a mixture of polybrominated diphenyl ethers (PBDEs) which has been widely used as a flame retardant. Since its ban in several countries it has been replaced by other brominated flame retardants such as hexabromocyclododecane (HBCD). Both certain PBDE congeners and HBCD are present in environmental and human samples reflecting their persistent and bioaccumulative properties. PentaBDE mix and HBCD have recently been found to induce cytochrome P450 (CYP) 3 enzymes in rat liver. In this study we tested both technical pentaBDE mix and HBCD for their potency to induce CYP3A enzymes in rat hepatocytes in primary culture, and in rat H4IIE and human HepG2 hepatoma cells. In rat hepatocytes, HBCD was a more effective CYP3A1 inducer than pentaBDE mix, being less effective, however, than the prototype inducer dexamethasone. In human HepG2 cells, both compounds and the prototype inducer rifampicin were about equally effective. In contrast, in HepG2 cells, HBCD failed to induce luciferin-PFBE dealkylase, a common catalytic activity of a number of CYP3A enzymes, possibly reflecting enzyme inhibition. A significant induction of catalytic activity was observed in rat hepatocytes with both compounds. Analysis of a XREM-driven reporter gene activity in transfected cells confirmed that both compounds act as agonists of the human and rat pregnane-X-receptor, which was detectable in all cell types used.

摘要

工业用五溴二苯醚(五溴二苯醚混合物)是一种多溴二苯醚(PBDEs)混合物,已被广泛用作阻燃剂。自其在多个国家被禁用以来,已被其他溴化阻燃剂如六溴环十二烷(HBCD)所取代。某些PBDE同系物和HBCD都存在于环境和人体样本中,这反映了它们的持久性和生物累积性。最近发现五溴二苯醚混合物和HBCD可诱导大鼠肝脏中的细胞色素P450(CYP)3酶。在本研究中,我们测试了工业用五溴二苯醚混合物和HBCD在原代培养的大鼠肝细胞以及大鼠H4IIE和人HepG2肝癌细胞中诱导CYP3A酶的能力。在大鼠肝细胞中,HBCD是比五溴二苯醚混合物更有效的CYP3A1诱导剂,然而,其效果不如原型诱导剂地塞米松。在人HepG2细胞中,这两种化合物和原型诱导剂利福平的效果大致相同。相比之下,在HepG2细胞中,HBCD未能诱导荧光素 - PFBE脱烷基酶,这是多种CYP3A酶的一种常见催化活性,可能反映了酶抑制作用。在大鼠肝细胞中观察到这两种化合物都能显著诱导催化活性。对转染细胞中XREM驱动的报告基因活性的分析证实,这两种化合物都作为人和大鼠孕烷X受体的激动剂,在所有使用的细胞类型中都可检测到。

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