Bile acid transport

被引:71
作者
Bahar, RJ
Stolz, A
机构
[1] Univ Calif Los Angeles, Sch Med, Dept Pediat, Div Gastroenterol & Nutr, Los Angeles, CA 90024 USA
[2] Univ So Calif, Dept Med, Div Gastrointestinal & Liver Dis, Los Angeles, CA USA
关键词
D O I
10.1016/S0889-8553(05)70042-X
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Bile acids undergo a unique enterohepatic circulation between the liver and intestine, where they are required for intestinal absorption of fatty acids and hydrophobic compounds. Recently, some of the key bile acid transporters in the liver and intestine have been identified, allowing for a vastly greater understanding of how these proteins normally operate. Mutations in specific bile acid transporters have recently been recognized in specific cholestatic syndromes, which usually appear in early childhood. Bile acid transporters are also being used to develop novel drug delivery systems that can enhance intestinal absorption or target delivery to the Liver. These recent advances in the fundamental biology of bile acid transporters will lead to the development of new therapies for general cholestatic liver disease and for inherited cholestatic diseases of childhood.
引用
收藏
页码:27 / +
页数:33
相关论文
共 175 条
  • [21] 7 alpha-dehydroxylating bacteria enhance deoxycholic acid input and cholesterol saturation of bile in patients with gallstones
    Berr, F
    KullakUblick, GA
    Paumgartner, G
    Munzing, W
    Hylemon, PB
    [J]. GASTROENTEROLOGY, 1996, 111 (06) : 1611 - 1620
  • [22] BENIGN RECURRENT INTRAHEPATIC CHOLESTASIS - ALTERED BILE-ACID METABOLISM
    BIJLEVELD, CMA
    VONK, RJ
    KUIPERS, F
    HAVINGA, R
    BOVERHOF, R
    KOOPMAN, BJ
    WOLTHERS, BG
    FERNANDES, J
    [J]. GASTROENTEROLOGY, 1989, 97 (02) : 427 - 432
  • [23] TREATMENT OF PATIENTS WITH BENIGN RECURRENT INTRAHEPATIC CHOLESTASIS
    BIRCHER, J
    [J]. HEPATOLOGY, 1989, 10 (06) : 1030 - 1030
  • [24] Byler-like familial cholestasis in an extended kindred
    Bourke, B
    Goggin, N
    Walsh, D
    Kennedy, S
    Setchell, KDR
    Drumm, B
    [J]. ARCHIVES OF DISEASE IN CHILDHOOD, 1996, 75 (03) : 223 - 227
  • [25] BOYER JL, 1990, METHOD ENZYMOL, V192, P517
  • [26] BENIGN RECURRENT INTRAHEPATIC CHOLESTASIS - A REPORT OF 26 CASES
    BRENARD, R
    GEUBEL, AP
    BENHAMOU, JP
    [J]. JOURNAL OF CLINICAL GASTROENTEROLOGY, 1989, 11 (05) : 546 - 551
  • [27] ENHANCED SECRETION OF GLYCOCHOLIC ACID IN A SPECIALLY ADAPTED CELL-LINE IS ASSOCIATED WITH OVEREXPRESSION OF APPARENTLY NOVEL ATP-BINDING CASSETTE PROTEINS
    BROWN, RS
    LOMRI, N
    DEVOSS, J
    RAHMAOUI, CM
    XIE, MH
    HUA, T
    LIDOFSKY, SD
    SCHARSCHMIDT, BF
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (12) : 5421 - 5425
  • [28] NONSYNDROMIC PAUCITY OF INTRAHEPATIC BILE-DUCTS IN INFANCY AND IDIOPATHIC DUCTOPENIA IN ADULTHOOD - THE SAME SYNDROME
    BRUGUERA, M
    LLACH, J
    RODES, J
    [J]. HEPATOLOGY, 1992, 15 (05) : 830 - 834
  • [29] A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis
    Bull, LN
    van Eijk, MJT
    Pawlikowska, L
    DeYoung, JA
    Juijn, JA
    Liao, M
    Klomp, LWJ
    Lomri, N
    Berger, R
    Scharschmidt, BF
    Knisely, AS
    Houwen, RHJ
    Freimer, NB
    [J]. NATURE GENETICS, 1998, 18 (03) : 219 - 224
  • [30] SUBCELLULAR AND MOLECULAR MECHANISMS OF BILE SECRETION
    BURWEN, SJ
    SCHMUCKER, DL
    JONES, AL
    [J]. INTERNATIONAL REVIEW OF CYTOLOGY-A SURVEY OF CELL BIOLOGY, 1992, 135 : 269 - 313