• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Identification of genes controlled by the pregnane X receptor by microarray analysis of mRNAs from pregnenolone 16alpha-carbonitrile-treated rats.通过对孕烯醇酮16α-腈处理大鼠的mRNA进行微阵列分析来鉴定由孕烷X受体调控的基因。
Toxicol Sci. 2006 Dec;94(2):379-87. doi: 10.1093/toxsci/kfl116. Epub 2006 Sep 22.
2
RNA-Seq reveals common and unique PXR- and CAR-target gene signatures in the mouse liver transcriptome.RNA测序揭示了小鼠肝脏转录组中常见和独特的孕烷X受体及组成型雄烷受体靶基因特征。
Biochim Biophys Acta. 2016 Sep;1859(9):1198-1217. doi: 10.1016/j.bbagrm.2016.04.010. Epub 2016 Apr 23.
3
Identification by differential display of the IF1 inhibitor peptide of ATP synthase/ATPase as a gene inducible in rat liver by pregnenolone 16alpha-carbonitrile.通过差异显示鉴定出ATP合酶/ATP酶的IF1抑制肽作为孕烯醇酮16α-腈在大鼠肝脏中诱导表达的基因。
Life Sci. 2000 Sep 1;67(15):1825-32. doi: 10.1016/s0024-3205(00)00769-4.
4
Regulation of mRNA expression of xenobiotic transporters by the pregnane x receptor in mouse liver, kidney, and intestine.孕烷X受体对小鼠肝脏、肾脏和肠道中外源物质转运体mRNA表达的调控。
Drug Metab Dispos. 2006 Nov;34(11):1863-7. doi: 10.1124/dmd.106.010520. Epub 2006 Aug 23.
5
Pregnenolone 16α-carbonitrile ameliorates concanavalin A-induced liver injury in mice independent of the nuclear receptor PXR activation.孕烯醇酮16α-腈可改善伴刀豆球蛋白A诱导的小鼠肝损伤,且与核受体孕烷X受体(PXR)激活无关。
Toxicol Lett. 2017 Apr 5;271:58-65. doi: 10.1016/j.toxlet.2017.02.018. Epub 2017 Feb 22.
6
The nuclear receptors pregnane X receptor and constitutive androstane receptor contribute to the impact of fipronil on hepatic gene expression linked to thyroid hormone metabolism.核受体孕烷 X 受体和组成型雄烷受体有助于氟虫腈对与甲状腺激素代谢相关的肝脏基因表达的影响。
Biochem Pharmacol. 2013 Oct 1;86(7):997-1039. doi: 10.1016/j.bcp.2013.08.012. Epub 2013 Aug 17.
7
Expression of PXR, CYP3A and MDR1 genes in liver of zebrafish.斑马鱼肝脏中PXR、CYP3A和MDR1基因的表达
Comp Biochem Physiol C Toxicol Pharmacol. 2005 Mar-Apr;140(3-4):403-7. doi: 10.1016/j.cca.2005.04.003.
8
Induction of rat organic anion transporting polypeptide 2 by pregnenolone-16alpha-carbonitrile is via interaction with pregnane X receptor.孕烯醇酮-16α-腈对大鼠有机阴离子转运多肽2的诱导作用是通过与孕烷X受体相互作用实现的。
Mol Pharmacol. 2002 Apr;61(4):832-9. doi: 10.1124/mol.61.4.832.
9
p53-independent induction of rat hepatic Mdm2 following administration of phenobarbital and pregnenolone 16alpha-carbonitrile.苯巴比妥和孕烯醇酮16α-腈给药后大鼠肝脏Mdm2的p53非依赖性诱导
Toxicol Sci. 2006 Dec;94(2):272-80. doi: 10.1093/toxsci/kfl115. Epub 2006 Sep 25.
10
Ectopic expression of MHC class II genes (RT1.B(I) beta/alpha) in rat hepatocytes in vivo and in culture can be elicited by treatment with the pregnane X receptor agonists pregnenolone 16 alpha-carbonitrile and dexamethasone.孕烷X受体激动剂孕烯醇酮16α-腈和地塞米松处理可在体内和体外培养的大鼠肝细胞中引发MHC II类基因(RT1.B(I)β/α)的异位表达。
Life Sci. 2002 Jun 7;71(3):311-23. doi: 10.1016/s0024-3205(02)01643-0.

引用本文的文献

1
PM Extracts Induce INFγ-Independent Activation of CIITA, MHCII, and Increases Inflammation in Human Bronchial Epithelium.颗粒物提取物可诱导人类支气管上皮细胞中不依赖干扰素γ的MHCII类反式激活因子(CIITA)激活,并增加炎症反应。
Toxics. 2024 Apr 16;12(4):292. doi: 10.3390/toxics12040292.
2
Pregnane X Receptor and the Gut-Liver Axis: A Recent Update.孕烷 X 受体与肠-肝轴:最新进展。
Drug Metab Dispos. 2022 Apr;50(4):478-491. doi: 10.1124/dmd.121.000415. Epub 2021 Dec 3.
3
RNA interference screen identifies NAA10 as a regulator of PXR transcription.RNA 干扰筛选鉴定 NAA10 为 PXR 转录的调节剂。
Biochem Pharmacol. 2019 Feb;160:92-109. doi: 10.1016/j.bcp.2018.12.012. Epub 2018 Dec 16.
4
Glucose-dependent regulation of pregnane X receptor is modulated by AMP-activated protein kinase.葡萄糖依赖性调节孕烷 X 受体受 AMP 激活的蛋白激酶调节。
Sci Rep. 2017 Apr 24;7:46751. doi: 10.1038/srep46751.
5
Induction of Drug Transporters Alters Disposition of Risperidone - A Study in Mice.药物转运体的诱导改变利培酮的处置——一项小鼠研究
Pharmaceutics. 2010 Jun 2;2(2):258-274. doi: 10.3390/pharmaceutics2020258.
6
The Effects of Pregnenolone 16α-Carbonitrile Dosing on Digoxin Pharmacokinetics and Intestinal Absorption in the Rat.孕烯醇酮16α-腈给药对大鼠地高辛药代动力学及肠道吸收的影响
Pharmaceutics. 2010 Mar 15;2(1):61-77. doi: 10.3390/pharmaceutics2010061.
7
Role of pregnane X receptor in chemotherapeutic treatment. pregnane X 受体在化疗治疗中的作用。
Cancer Chemother Pharmacol. 2014 Aug;74(2):217-27. doi: 10.1007/s00280-014-2494-9. Epub 2014 Jun 3.
8
Using molecular features of xenobiotics to predict hepatic gene expression response.利用外源化学物的分子特征预测肝脏基因表达反应。
J Chem Inf Model. 2013 Oct 28;53(10):2765-73. doi: 10.1021/ci3005868. Epub 2013 Oct 2.
9
Rifampicin Does not Significantly Affect the Expression of Small Heterodimer Partner in Primary Human Hepatocytes.利福平对原代人肝细胞中小异源二聚体伴侣的表达无显著影响。
Front Pharmacol. 2012 Jan 19;3:1. doi: 10.3389/fphar.2012.00001. eCollection 2012.
10
Pregnane X receptor regulates drug metabolism and transport in the vasculature and protects from oxidative stress. pregnane X 受体调节血管中的药物代谢和转运,并防止氧化应激。
Cardiovasc Res. 2012 Mar 15;93(4):674-81. doi: 10.1093/cvr/cvr330. Epub 2011 Dec 13.

本文引用的文献

1
The CAR nuclear receptor and hepatocyte proliferation.CAR核受体与肝细胞增殖。
Hepatology. 2005 Nov;42(5):1004-8. doi: 10.1002/hep.20953.
2
Gadd45beta is induced through a CAR-dependent, TNF-independent pathway in murine liver hyperplasia.在小鼠肝脏增生过程中,Gadd45β是通过一种依赖于CAR且不依赖于TNF的途径被诱导产生的。
Hepatology. 2005 Nov;42(5):1118-26. doi: 10.1002/hep.20883.
3
The nuclear xenobiotic receptor pregnane X receptor: recent insights and new challenges.核外源性物质受体孕烷X受体:最新见解与新挑战
Mol Endocrinol. 2005 Dec;19(12):2891-900. doi: 10.1210/me.2005-0156. Epub 2005 Jun 16.
4
The molecular physiology of tight junction pores.紧密连接孔的分子生理学
Physiology (Bethesda). 2004 Dec;19:331-8. doi: 10.1152/physiol.00027.2004.
5
PXR (NR1I2): splice variants in human tissues, including brain, and identification of neurosteroids and nicotine as PXR activators.孕烷X受体(NR1I2):人体组织(包括大脑)中的剪接变体,以及神经甾体和尼古丁作为孕烷X受体激活剂的鉴定。
Toxicol Appl Pharmacol. 2004 Sep 15;199(3):251-65. doi: 10.1016/j.taap.2003.12.027.
6
Vitamin K2 regulation of bone homeostasis is mediated by the steroid and xenobiotic receptor SXR.维生素K2对骨稳态的调节是由类固醇和外源性物质受体SXR介导的。
J Biol Chem. 2003 Nov 7;278(45):43919-27. doi: 10.1074/jbc.M303136200. Epub 2003 Aug 14.
7
Nuclear receptors orchestrate detoxification pathways.核受体调控解毒途径。
Dev Cell. 2003 May;4(5):607-8. doi: 10.1016/s1534-5807(03)00131-x.
8
Genetic profiling defines the xenobiotic gene network controlled by the nuclear receptor pregnane X receptor.基因谱分析确定了由核受体孕烷X受体控制的外源性物质基因网络。
Mol Endocrinol. 2003 Jul;17(7):1268-82. doi: 10.1210/me.2002-0421. Epub 2003 Mar 27.
9
The nuclear receptor PXR: a master regulator of "homeland" defense.核受体PXR:“本土”防御的主要调节因子。
Crit Rev Eukaryot Gene Expr. 2002;12(1):53-64. doi: 10.1615/critreveukaryotgeneexpr.v12.i1.30.
10
Nuclear pregnane x receptor and constitutive androstane receptor regulate overlapping but distinct sets of genes involved in xenobiotic detoxification.核孕烷X受体以及组成型雄烷受体调控参与外源性物质解毒的重叠但不同的基因集。
Mol Pharmacol. 2002 Sep;62(3):638-46. doi: 10.1124/mol.62.3.638.

通过对孕烯醇酮16α-腈处理大鼠的mRNA进行微阵列分析来鉴定由孕烷X受体调控的基因。

Identification of genes controlled by the pregnane X receptor by microarray analysis of mRNAs from pregnenolone 16alpha-carbonitrile-treated rats.

作者信息

Guzelian Jeffrey, Barwick Joyce L, Hunter Lawrence, Phang Tzu L, Quattrochi Linda C, Guzelian Philip S

机构信息

Department of Medicine, University of Colorado, Boulder, Colorado 80262, USA.

出版信息

Toxicol Sci. 2006 Dec;94(2):379-87. doi: 10.1093/toxsci/kfl116. Epub 2006 Sep 22.

DOI:10.1093/toxsci/kfl116
PMID:16997903
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1636678/
Abstract

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.

摘要

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。