期刊文献+

代谢性核受体功能及转录活性调控机制的研究进展 被引量:3

Progress in the function and transcriptional regulation mechanism of metabolic nuclear receptor
下载PDF
导出
摘要 代谢性核受体隶属于配体依赖性转录因子超家族,其下游效应靶基因均为主司异源性药物/毒物及内源性激素代谢功能的酶及转运蛋白,可对临床药物治疗效果及疾病易感性产生重要的影响。近年来有关代谢性核受体的功能及其转录活性调控的机制等已开始受到了关注,并已成为药物代谢动力学及临床肝病治疗学领域新的研究热点。 Metabolic nuclear receptors belong to a superfamily of ligandactivated transcription factors, which regulates the expression of enzyme and transport protein responsing for metabolizing xenobiotics and endogenous hormones, contributed to the therapeutic effect of drug and susceotility for diseases. Recently, it has been interested in the function of the metabolic nuclear receptors and their transcriptional regulation mechanism by the ligands, and the researches have been focused on pharmacokinectics and clinical hepatopathy treatment field.
出处 《中国临床药理学杂志》 CAS CSCD 北大核心 2009年第4期346-349,共4页 The Chinese Journal of Clinical Pharmacology
关键词 代谢性核受体 配体 转录活性调节 metabolic nuclear receptor ligand transcriptional regulatio
  • 相关文献

参考文献13

  • 1Jacobs MN, Nolanb GT, Hoodb SR. Lignans, bacteriocides and organochlorine compounds activate the human pregnane X receptor (PXR) [J]. Toxicol Appl Pharm, 2005 ;209:123-133.
  • 2Iwazaki N, Kobayashi K, Mofimoto K, et al. Involvement of hepatocyte nuclear factor 4alpha in transcriptional regulation of the human pregnane X receptor gene in the human liver[J]. Drug Metab Pharmacokirtet, 2008;23 : 59-66.
  • 3Takagi S, Nakajima M, Mohri T, et al. Post-transcriptional regulation of human pregnane X receptor by microRNA affects the expression of cytochrome P450 3A4 [ J ]. J Biol Chem, 2008 ; 283 : 9674- 9680.
  • 4Mnif W, Pascussi JM, Pillon A, et al. Estrogens and antiestrogens activate hPXR[ J]. Toxicol Lett,2007 ;170:19-29.
  • 5Wang H, Li H, Moore LB, et al. The phytoestrogen coumestrol is a naturally-occurring antagonist of the human pregnane X receptor (PXR) [ J]. Mol Endocrinol,2008 ;2 : 838-857.
  • 6Healan-Greenberg C, Waxing JF, Kempf D J, et al. HIV protease inhibitor A-792611 is a novel functional inhibitor of human PXR[ J ]. Drug Metab Dispos , 2008 ;36:500-507.
  • 7Chintlli V, Longo V, Marini S, et al. CAR and PXR expression and inducibility of CYP2B and CYP3A activities in rat and rabbit lungs [ J]. Life Sci,2005 ;76:2535-2546.
  • 8Pustylnyak VO, Gulyaeva LF, Lyakhovich VV. CAR expression and inducibility of CYP2B genes in liver of rats treated with PB-like inducers[J]. Toxicology, 2005;216:147-153.
  • 9Surapureddi S, Rana R, Reddy JK, et al. The coactivator NCOA6 mediates the synergistic activation of human cytochrome P4502C9 by the constitutive androstane receptor and hepatic nuclear factor-4α [ J ] . Mol Pharmacol,2008; 13 (in press).
  • 10Sagredo C, Φvrebφ S, Haugena A, et al. Quantitative analysis of benzo[ a ] pyrene biotransformation and adduct formation in Ahr knockout mice[J]. Toxicol Lett, 2006; 167:173-182.

同被引文献25

引证文献3

二级引证文献7

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部