Essential roles of bile acids and their nuclear receptors, FXR and PXR, in the cholestatic liver disease

被引:3
|
作者
Han, Bumin [1 ]
Kim, Byung-Kwon [1 ]
Kim, Kyumin [1 ]
Fang, Sungsoon [1 ]
机构
[1] Sejong Univ, Coll Life Sci, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
Bile acids; Farnesoid X receptor; Pregnane X receptor; PRIMARY BILIARY-CIRRHOSIS; URSODEOXYCHOLIC ACID; HCO3-UMBRELLA; PATHOGENESIS; INJURY;
D O I
10.1080/19768354.2016.1211175
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Bile acids (BAs) are steroid acids found predominantly in the bile of mammals and other vertebrates. Though BAs have been known as digestive juice, recent studies have revealed that BAs act as signaling molecules to control metabolism and inflammation. Today, BAs are considered as potential therapeutic molecules for treatment of complex metabolic liver disease. However, the detergent properties of BAs lead to hepatic injury and intrahepatic cholestasis when BAs are accumulated in the liver with impaired bile flow into gall bladder. Cholestasis is a pathological condition of hepatic retention of cytotoxic bile acids. To date, hydrophilic ursodeoxycholic acid has been currently used to treat cholestasis, but the efficacy of UDCA for cholestasis is still limited. Given that BAs are endogenous ligands of several nuclear receptors, including Farnesoid X receptor and Pregnane X receptor, novel synthetic ligands for those nuclear receptors are promising for the treatment of cholestatic liver diseases.
引用
收藏
页码:175 / 178
页数:4
相关论文
共 50 条
  • [21] Nuclear Receptors, Inflammation, and Liver Disease: Insights for Cholestatic and Fatty Liver Diseases
    Arrese, M.
    Karpen, S. J.
    CLINICAL PHARMACOLOGY & THERAPEUTICS, 2010, 87 (04) : 473 - 478
  • [22] Impact of Nuclear Receptors CAR, PXR, FXR, and VDR, and Their Ligands On Enzymes and Transporters
    Tirona, Rommel G.
    ENZYME- AND TRANSPORTER-BASED DRUG-DRUG INTERACTIONS: PROGRESS AND FUTURE CHALLENGES, 2010, : 75 - 105
  • [23] Targeting Nuclear Bile Acid Receptors for Liver Disease
    Trauner, Michael
    Baghdasaryan, Anna
    Claudel, Thierry
    Fickert, Peter
    Halilbasic, Emina
    Moustafa, Tarek
    Zollner, Gernot
    DIGESTIVE DISEASES, 2011, 29 (01) : 98 - 102
  • [24] Bile Acids and FXR: Novel Targets for Liver Diseases
    Stofan, Mary
    Guo, Grace L.
    FRONTIERS IN MEDICINE, 2020, 7
  • [25] Bile Acids as Signaling Molecules: Role of Ursodeoxycholic Acid in Cholestatic Liver Disease
    Cifuentes-Silva, Eduardo
    Cabello-Verrugio, Claudio
    CURRENT PROTEIN & PEPTIDE SCIENCE, 2024, 25 (03) : 206 - 214
  • [26] The roles of nuclear receptors CAR and PXR in hepatic energy metabolism
    Konno, Yoshihiro
    Negishi, Masahiko
    Kodama, Susumu
    DRUG METABOLISM AND PHARMACOKINETICS, 2008, 23 (01) : 8 - 13
  • [27] Endogenous bile acids are ligands for the nuclear receptor FXR BAR
    Wang, HB
    Chen, J
    Hollister, K
    Sowers, LC
    Forman, BM
    MOLECULAR CELL, 1999, 3 (05) : 543 - 553
  • [28] Bile acid metabolism and FXR-mediated effects in human cholestatic liver disorders
    Molinaro, Antonio
    Marschall, Hanns-Ulrich
    BIOCHEMICAL SOCIETY TRANSACTIONS, 2022, 50 (01) : 361 - 373
  • [29] Inappropriate ileal conservation of bile acids in cholestatic liver disease: homeostasis gone awry
    Hofmann, AF
    GUT, 2003, 52 (09) : 1239 - 1241
  • [30] Hepatic levels of bile acids in end-stage chronic cholestatic liver disease
    Fischer, S
    Beuers, U
    Spengler, U
    Zwiebel, FM
    Koebe, HG
    CLINICA CHIMICA ACTA, 1996, 251 (02) : 173 - 186