The Farnesoid X Receptor: Good for BAD

被引:50
作者
Keely, Stephen J. [1 ]
Walters, Julian R. F. [2 ]
机构
[1] Beaumont Hosp, Educ & Res Ctr, Royal Coll Surg Ireland, Mol Med Labs, Smurfit Bldg, Dublin 9, Ireland
[2] Imperial Coll London, Hammersmith Hosp, Div Digest Dis, London, England
来源
CELLULAR AND MOLECULAR GASTROENTEROLOGY AND HEPATOLOGY | 2016年 / 2卷 / 06期
基金
爱尔兰科学基金会;
关键词
Bile Acid Diarrhea; Enterohepatic Circulation; FGF-19; Chloride Secretion; Epithelium;
D O I
10.1016/j.jcmgh.2016.08.004
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Diarrhea is a feature of several chronic intestinal disorders that are associated with increased delivery of bile acids into the colon. Although the prevalence of bile acid diarrhea is high, affecting approximately 1% of the adult population, current therapies often are unsatisfactory. By virtue of its capacity to inhibit colonic epithelial fluid secretion and to down-regulate hepatic bile acid synthesis through induction of the ileal fibroblast growth factor 19 release, the nuclear bile acid receptor, farnesoid X receptor, represents a promising target for the development of new therapeutic approaches. Here, we review our current understanding of the pathophysiology of bile acid diarrhea and the current evidence supporting a role for farnesoid X receptor agonists in treatment of the disease.
引用
收藏
页码:725 / 732
页数:8
相关论文
共 70 条
  • [1] The Receptor TGR5 Mediates the Prokinetic Actions of Intestinal Bile Acids and Is Required for Normal Defecation in Mice
    Alemi, Farzad
    Poole, Daniel P.
    Chiu, Jonathan
    Schoonjans, Kristina
    Cattaruzza, Fiore
    Grider, John R.
    Bunnett, Nigel W.
    Corvera, Carlos U.
    [J]. GASTROENTEROLOGY, 2013, 144 (01) : 145 - 154
  • [2] Taurodeoxycholate modulates apical Cl-/OH- exchange activity in Caco2 cells
    Alrefai, Waddah A.
    Saksena, Seema
    Tyagi, Sangeeta
    Gill, Ravinder K.
    Ramaswamy, Krishnamurthy
    Dudeja, Pradeep K.
    [J]. DIGESTIVE DISEASES AND SCIENCES, 2007, 52 (05) : 1270 - 1278
  • [3] EFFECT OF CONJUGATED DIHYDROXY BILE-SALTS ON ELECTROLYTE TRANSPORT IN RAT COLON
    BINDER, HJ
    RAWLINS, CL
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1973, 52 (06) : 1460 - 1466
  • [4] BREUER NF, 1983, GASTROENTEROLOGY, V84, P969
  • [5] PHARMACOLOGICAL INHIBITION OF CHENODEOXYCHOLATE-INDUCED FLUID AND MUCUS SECRETION AND MUCOSAL INJURY IN THE RABBIT COLON
    CAMILLERI, M
    MURPHY, R
    CHADWICK, VS
    [J]. DIGESTIVE DISEASES AND SCIENCES, 1982, 27 (10) : 865 - 869
  • [6] Effect of Increased Bile Acid Synthesis or Fecal Excretion in Irritable Bowel Syndrome-Diarrhea
    Camilleri, Michael
    Busciglio, Irene
    Acosta, Andres
    Shin, Andrea
    Carlson, Paula
    Burton, Duane
    Ryks, Michael
    Rhoten, Deborah
    Lamsam, Jesse
    Lueke, Alan
    Donato, Leslie J.
    Zinsmeister, Alan R.
    [J]. AMERICAN JOURNAL OF GASTROENTEROLOGY, 2014, 109 (10) : 1621 - 1630
  • [7] Bile acid transporters
    Dawson, Paul A.
    Lan, Tian
    Rao, Anuradha
    [J]. JOURNAL OF LIPID RESEARCH, 2009, 50 (12) : 2340 - 2357
  • [8] TAURODEOXYCHOLATE ACTIVATES POTASSIUM AND CHLORIDE CONDUCTANCES VIA AN IP3-MEDIATED RELEASE OF CALCIUM FROM INTRACELLULAR STORES IN A COLONIC CELL-LINE (T84)
    DEVOR, DC
    SEKAR, MC
    FRIZZELL, RA
    DUFFEY, ME
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (05) : 2173 - 2181
  • [9] CL- SECRETION INDUCED BY BILE-SALTS - A STUDY OF THE MECHANISM OF ACTION BASED ON A CULTURED COLONIC EPITHELIAL-CELL LINE
    DHARMSATHAPHORN, K
    HUOTT, PA
    VONGKOVIT, P
    BEUERLEIN, G
    PANDOL, SJ
    AMMON, HV
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (03) : 945 - 953
  • [10] HUMAN GUT MUCOSAL MAST-CELLS - ULTRASTRUCTURAL OBSERVATIONS AND ANATOMIC VARIATION IN MAST CELL-NERVE ASSOCIATIONS INVIVO
    DVORAK, AM
    MCLEOD, RS
    ONDERDONK, AB
    MONAHANEARLEY, RA
    CULLEN, JB
    ANTONIOLI, DA
    MORGAN, E
    BLAIR, JE
    ESTRELLA, P
    CISNEROS, RL
    COHEN, Z
    SILEN, W
    [J]. INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 1992, 98 (02) : 158 - 168