PXR- and CAR-mediated herbal effect on human diseases

被引:23
作者
Xu, Chenshu [2 ]
Huang, Min [1 ]
Bi, Huichang [1 ]
机构
[1] Sun Yat Sen Univ, Sch Pharmaceut Sci, Lab Drug Metab & Pharmacokinet, Guangzhou 510006, Guangdong, Peoples R China
[2] Shenzhen Univ, Sch Med, Dept Pharm, Shenzhen 518060, Guangdong, Peoples R China
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS | 2016年 / 1859卷 / 09期
关键词
Pregnane X receptor; Constitutive androstane receptor; Herbal medicine; Human diseases; PREGNANE-X-RECEPTOR; CONSTITUTIVE ANDROSTANE RECEPTOR; INFLAMMATORY-BOWEL-DISEASE; ST JOHNS WORT; GINKGO-BILOBA EXTRACT; MDR1; GENE-EXPRESSION; TANSHINONE IIA; NUCLEAR RECEPTORS; UP-REGULATION; DRUG-METABOLISM;
D O I
10.1016/j.bbagrm.2016.02.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The pregnane X receptor (PXR) and constitutive androstane receptor (CAR) are two members of the nuclear receptor superfamily that regulate a broad range of genes involved in drug metabolism and transport. A variety of naturally occurring compounds present in herbal medicines were identified as ligands of PXR and CAR. Recently, accumulative evidences have revealed the PXR- and CAR-mediated herbal effect against multiple human diseases, including inflammatory bowel disease (IBD), cholestatic liver disease, and jaundice. The current review summarized the recent progress in identifying the expanding libraries of herbal medicine as ligands for PXR and CAR. Moreover, the potential for herbal medicines as promising therapeutic agents which were mainly regulated through PXR/CAR signaling pathways was also discussed. The discovery of herbal medicines as modulators of PXR and CAR, and their PXR- and CAR-mediated effect on human diseases will provide a basis for rational drug design, and eventually be explored as a novel therapeutic approach against human diseases. This article is part of a Special Issue entitled: Xenobiotic nuclear receptors: New Tricks for An Old Dog, edited by Dr. Wen Xie. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:1121 / 1129
页数:9
相关论文
共 108 条
[1]
Expression of the drug transporters MDR1/ABCB1, MRP1/ABCC1, MRP2/ABCC2, BCRP/ABCG2, and PXR in peripheral blood mononuclear cells and their relationship with the expression in intestine and liver [J].
Albermann, N ;
Schmitz-Winnenthal, FH ;
Z'graggen, K ;
Volk, C ;
Hoffmann, MM ;
Haefeli, WE ;
Weiss, J .
BIOCHEMICAL PHARMACOLOGY, 2005, 70 (06) :949-958
[2]
INHIBITION OF GLUCONEOGENESIS IN ISOLATED RAT HEPATOCYTES AFTER CHRONIC TREATMENT WITH PHENOBARBITAL [J].
ARGAUD, D ;
HALIMI, S ;
CATELLONI, F ;
LEVERVE, XM .
BIOCHEMICAL JOURNAL, 1991, 280 :663-669
[3]
Interactions between hepatic Mrp4 and Sult2a as revealed by the constitutive androstane receptor and Mrp4 knockout mice [J].
Assem, M ;
Schuetz, EG ;
Leggas, M ;
Sun, DX ;
Yasuda, K ;
Reid, G ;
Zelcer, N ;
Adachi, M ;
Strom, S ;
Evans, RM ;
Moore, DD ;
Borst, P ;
Schuetz, JD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (21) :22250-22257
[4]
New paradigms in the treatment of hepatic cholestasis: From UDCA to FXR, PXR and beyond [J].
Beuers, Ulrich ;
Trauner, Michael ;
Jansen, Peter ;
Poupon, Raoul .
JOURNAL OF HEPATOLOGY, 2015, 62 :S25-S37
[5]
Diagnostic criteria for neuropathologic assessment of Alzheimer's disease [J].
Braak, H ;
Braak, E .
NEUROBIOLOGY OF AGING, 1997, 18 (04) :S85-S88
[6]
Guggulsterone activates multiple nuclear receptors and induces CYP3A gene expression through the pregnane X receptor [J].
Brobst, DE ;
Ding, XS ;
Creech, KL ;
Goodwin, B ;
Kelley, B ;
Staudinger, JL .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2004, 310 (02) :528-535
[7]
Antimalarial artemisinin drugs induce cytochrome p450 and MDR1 expression by activation of xenosensors pregnane X receptor and constitutive androstane receptor [J].
Burk, O ;
Arnold, KA ;
Nussler, AK ;
Schaeffeler, E ;
Efimova, E ;
Avery, BA ;
Avery, MA ;
Fromm, MF ;
Eichelbaum, M .
MOLECULAR PHARMACOLOGY, 2005, 67 (06) :1954-1965
[8]
Chai J, 2015, INT J CLIN EXP MED, V8, P1691
[9]
Ginkgo biloba leave extract:: Biological, medicinal, and toxicological effects [J].
Chan, Po-Chuen ;
Xia, Qingsu ;
Fu, Peter P. .
JOURNAL OF ENVIRONMENTAL SCIENCE AND HEALTH PART C-ENVIRONMENTAL CARCINOGENESIS & ECOTOXICOLOGY REVIEWS, 2007, 25 (03) :211-244
[10]
Low Dose of Oleanolic Acid Protects against Lithocholic Acid-Induced Cholestasis in Mice: Potential Involvement of Nuclear Factor-E2-Related Factor 2-Mediated Upregulation of Multidrug Resistance-Associated Proteins [J].
Chen, Pan ;
Zeng, Hang ;
Wang, Yongtao ;
Fan, Xiaomei ;
Xu, Chenshu ;
Deng, Rongrong ;
Zhou, Xunian ;
Bi, Huichang ;
Huang, Min .
DRUG METABOLISM AND DISPOSITION, 2014, 42 (05) :844-852