Schuetz E G, Brimer C, Schuetz J D
Department of Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, Tennessee 38105, USA.
Mol Pharmacol. 1998 Dec;54(6):1113-7. doi: 10.1124/mol.54.6.1113.
The pregnenolone X receptor (PXR), a new member of the nuclear hormone receptor superfamily, was recently demonstrated to mediate glucocorticoid agonist and antagonist activation of a hormone response element spaced by three nucleotides (DR-3) within the rat CYP3A23 promoter. Because many other steroids and xenobiotics can up-regulate CYP3A23 expression, we determined whether some of these other regulators used PXR to activate the CYP3A23 DR-3. Transient co-transfection of LLC-PK1 cells with (CYP3A23)2-tk-CAT and mouse PXR demonstrated that the organochlorine pesticides transnonachlor and chlordane and the nonplanar polychlorinated biphenyls (PCBs) each induced the CYP3A23 DR-3 element, and this activation required PXR. Additionally, this study found that PXR is activated to induce (CYP3A23)2-tk-CAT by antihormones of several steroid classes including the antimineralocorticoid spironolactone and the antiandrogen cyproterone acetate. These studies reveal that PXR is involved in the induction of CYP3A23 by pharmacologically and structurally distinct steroids and xenobiotics. Moreover, PXR-mediated PCB activation of the (CYP3A23)2-tk-CAT may serve as a rapid assay for effects of nonplanar PCBs.
孕烯醇酮X受体(PXR)是核激素受体超家族的一个新成员,最近有研究表明它可介导糖皮质激素激动剂和拮抗剂对大鼠CYP3A23启动子内一个由三个核苷酸间隔的激素反应元件(DR-3)的激活。由于许多其他类固醇和外源性物质可上调CYP3A23的表达,我们确定这些其他调节因子中是否有一些利用PXR来激活CYP3A23 DR-3。LLC-PK1细胞与(CYP3A23)2-tk-CAT和小鼠PXR进行瞬时共转染实验表明,有机氯农药反式九氯和氯丹以及非平面多氯联苯(PCBs)均可诱导CYP3A23 DR-3元件,且这种激活需要PXR。此外,该研究发现,几种类固醇类别的抗激素,包括抗盐皮质激素螺内酯和抗雄激素醋酸环丙孕酮,均可激活PXR以诱导(CYP3A23)2-tk-CAT。这些研究表明,PXR参与了药理学和结构上不同的类固醇及外源性物质对CYP3A23的诱导。此外,PXR介导的(CYP3A23)2-tk-CAT的PCB激活作用可作为一种快速检测非平面PCBs效应的方法。