...
首页> 外文期刊>Drug metabolism and pharmacokinetics. >Peroxisome Proliferator-activated Receptor Alpha (PPARα) Agonists Induce Constitutive Androstane Receptor (CAR) and Cytochrome P450 2B in Rat Primary Hepatocytes
【24h】

Peroxisome Proliferator-activated Receptor Alpha (PPARα) Agonists Induce Constitutive Androstane Receptor (CAR) and Cytochrome P450 2B in Rat Primary Hepatocytes

机译:过氧化物酶体增殖物激活受体α(PPARα)激动剂在大鼠原代肝细胞中诱导组成型雄激素受体(CAR)和细胞色素P450 2B

获取原文
           

摘要

The constitutive androstane receptor (CAR; NR1I3) is a key transcriptional factor that regulates genes encoding drug-metabolizing enzymes and drug transporters. However, studies on regulation of CAR target genes via up- or down-regulation of CAR are limited. In this study, we examined the effects of PPARα agonists (ciprofibrate, bezafibrate, fenofibrate and WY14643) on the expression of CAR and its target gene CYP2B1/2 in rat primary hepatocytes. Results from real-time PCR analysis showed that CAR and CYP2B1/2 mRNAs exhibit increases in response to all PPARα agonists studied (5 to 10-folds of control). Pretreatment of cells with cycloheximide, an inhibitor of protein synthesis, completely suppressed increase in CYP2B1/2 mRNA in response to ciprofibrate, suggesting that protein synthesis is required in this process. In addition, the induction of CAR by ciprofibrate on the protein level was observed with nuclear extracts as well as total cell lysates. These results indicate that CYP2B1/2 mRNAs are induced by PPARα agonists and that this effect is accompanied by increase in the expression of CAR gene at both mRNA and nuclear protein levels. Activated PPARα may increase functional CAR protein, which can induce the expression of CAR target genes such as CYP2B.
机译:组成型雄甾烷受体(CAR; NR1I3)是调节编码药物代谢酶和药物转运蛋白的基因的关键转录因子。然而,关于通过CAR的上调或下调来调节CAR靶基因的研究是有限的。在这项研究中,我们检查了PPARα激动剂(环丙贝特,苯扎贝特,非诺贝特和WY14643)对大鼠原代肝细胞中CAR及其靶基因CYP2B1 / 2表达的影响。实时PCR分析的结果表明,CAR和CYP2B1 / 2 mRNA对所有研究的PPARα激动剂均表现出增加的作用(是对照的5至10倍)。用环己酰亚胺(一种蛋白质合成抑制剂)对细胞进行预处理可完全抑制CYP2B1 / 2 mRNA对环丙贝特的响应,表明在此过程中需要蛋白质合成。另外,用核提取物以及总细胞裂解物观察到环丙贝特在蛋白质水平上诱导CAR。这些结果表明CYP2B1 / 2 mRNAs是由PPARα激动剂诱导的,并且该效应伴随着mRNA和核蛋白水平上CAR基因表达的增加。活化的PPARα可能会增加功能性CAR蛋白,从而诱导CYP2B等CAR靶基因的表达。

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