Guzelian Jeffrey, Barwick Joyce L, Hunter Lawrence, Phang Tzu L, Quattrochi Linda C, Guzelian Philip S
Department of Medicine, University of Colorado, Boulder, Colorado 80262, USA.
Toxicol Sci. 2006 Dec;94(2):379-87. doi: 10.1093/toxsci/kfl116. Epub 2006 Sep 22.
Mammalian liver contains a pregnane X receptor (PXR, NR1I2), which binds drugs and other xenobiotics, and stimulates (or suppresses) expression of numerous genes involved in the metabolic elimination of foreign compounds and some toxic endogenous substances. In the present study, we used microarray analysis to identify genes whose expression in rat liver was significantly altered by pregnenolone 16alpha-carbonitrile (PCN) treatment. PCN is a synthetic steroid that induces cytochrome P4503A expression and is hepatoprotective by increasing resistance to subsequent stressful insults. Significant induction was seen for 138 genes while expression of 82 genes was significantly repressed. We found induction of genes known to be induced by PCN, such as enzymes involved in drug metabolism and transport. In addition, many genes were differentially expressed whose functions concerned intracellular metabolism, transport of essential small molecules, cell cycle, and redox balance. Our results support the idea that the domain of PXR-controlled gene networks may be even more extensive than currently thought and may extend to functions apart from xenobiotic metabolism.
哺乳动物肝脏含有孕烷X受体(PXR,NR1I2),该受体可与药物及其他外源性物质结合,并刺激(或抑制)众多参与外源化合物和一些有毒内源性物质代谢消除的基因的表达。在本研究中,我们使用微阵列分析来鉴定其在大鼠肝脏中的表达因孕烯醇酮16α-腈(PCN)处理而发生显著改变的基因。PCN是一种合成类固醇,可诱导细胞色素P4503A的表达,并通过增加对后续应激性损伤的抵抗力而具有肝脏保护作用。138个基因出现显著诱导,而82个基因的表达被显著抑制。我们发现了已知可被PCN诱导的基因的诱导情况,例如参与药物代谢和转运的酶。此外,许多功能涉及细胞内代谢、必需小分子的转运、细胞周期和氧化还原平衡的基因存在差异表达。我们的结果支持这样一种观点,即PXR控制的基因网络的范围可能比目前认为的更为广泛,并且可能扩展到除异源物质代谢之外的功能。