Bile acids: regulation of apoptosis by ursodeoxycholic acid

被引:274
|
作者
Amaral, Joana D. [1 ]
Viana, Ricardo J. S. [1 ]
Ramalho, Rita M. [1 ]
Steer, Clifford J. [2 ,3 ,4 ]
Rodrigues, Cecilia M. P. [1 ]
机构
[1] Univ Lisbon, Fac Pharm, Res Inst Med & Pharmaceut Sci, P-1699 Lisbon, Portugal
[2] Univ Minnesota, Sch Med, Dept Med, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Sch Med, Dept Genet, Minneapolis, MN 55455 USA
[4] Univ Minnesota, Sch Med, Dept Dev & Cell Biol, Minneapolis, MN 55455 USA
关键词
Bcl-2; family; cell death; liver; neuroprotection; nuclear steroid receptors; FARNESOID-X-RECEPTOR; PRIMARY RAT HEPATOCYTES; CYTOCHROME-C RELEASE; MITOCHONDRIAL-MEMBRANE PERMEABILIZATION; GLUCOCORTICOID-INDUCED APOPTOSIS; LIGAND-INDEPENDENT ACTIVATION; NEGATIVE FEEDBACK-REGULATION; NUCLEAR STEROID-RECEPTORS; PEPTIDE-INDUCED APOPTOSIS; CELL-SURFACE TRAFFICKING;
D O I
10.1194/jlr.R900011-JLR200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bile acids are a group of molecular species of acidic steroids with peculiar physical-chemical and biological characteristics. At high concentrations they become toxic to mammalian cells, and their presence is pertinent in the pathogenesis of several liver diseases and colon cancer. Bile acid cytoxicity has been related to membrane damage, but also to nondetergent effects, such as oxidative stress and apoptosis. Strikingly, hydrophilic ursodeoxycholic acid (UDCA), and its taurine-conjugated form (TUDCA), show profound cytoprotective properties. Indeed, these molecules have been described as potent inhibitors of classic pathways of apoptosis, although their precise mode of action remains to be clarified. UDCA, originally used for cholesterol gallstone dissolution, is currently considered the first choice therapy for several forms of cholestatic syndromes. However, the beneficial effects of both UDCA and TUDCA have been tested in other experimental pathological conditions with deregulated levels of apoptosis, including neurological disorders, such as Alzheimer's, Parkinson's, and Huntington's diseases. Here, we review the role of bile acids in modulating the apoptosis process, emphasizing the anti-apoptotic effects of UDCA and TUDCA, as well as their potential use as novel and alternate therapeutic agents for the treatment of apoptosis-related diseases., J. D., R. J. S. Viana, R. M. Ramalho, C. J. Steer, and C. M. P. Rodrigues. Bile acids: regulation of apoptosis by ursodeoxycholic acid. J. Lipid Res. 2009. 50: 1721-1734.
引用
收藏
页码:1721 / 1734
页数:14
相关论文
共 50 条
  • [31] DIFFERENCES IN CHENODEOXYCHOLIC ACID AND URSODEOXYCHOLIC ACID INFLUENCE ON RAT SMALL INTESTINAL WALL BILE-ACIDS
    KURTZ, W
    LEUSCHNER, U
    SCHOLZ, G
    MICHEL, J
    STROHM, WD
    ITALIAN JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 1980, 12 (04): : 331 - 334
  • [32] Ursodeoxycholic acid accelerates bile acid enterohepatic circulation
    Zhang, Yunjing
    Jiang, Runqiu
    Zheng, Xiaojiao
    Lei, Sha
    Huang, Fengjie
    Xie, Guoxiang
    Kwee, Sandi
    Yu, Herbert
    Farrar, Christine
    Sun, Beicheng
    Zhao, Aihua
    Jia, Wei
    BRITISH JOURNAL OF PHARMACOLOGY, 2019, 176 (16) : 2848 - 2863
  • [33] ON ORIGIN OF LITHOCHOLIC AND URSODEOXYCHOLIC ACIDS IN MAN - BILE ACIDS AND STEROIDS 106
    HELLSTROM, K
    SJOVALL, J
    ACTA PHYSIOLOGICA SCANDINAVICA, 1961, 51 (2-3): : 218 - &
  • [34] EFFECT OF URSODEOXYCHOLIC ACID ADMINISTRATION ON BILE-ACID COMPOSITION IN HAMSTER BILE
    MATEJKA, M
    VESCINA, C
    CARDUCCI, CN
    ALAYON, A
    DIOS, A
    SCARLATTO, E
    MAMIANETTI, A
    PHARMACOLOGICAL RESEARCH, 1990, 22 (03) : 297 - 305
  • [35] Different bile acids exhibit distinct biological effects: The tumor promoter deoxycholic acid induces apoptosis and the chemopreventive agent ursodeoxycholic acid inhibits cell proliferation
    Martinez, JD
    Stratagoules, ED
    LaRue, JM
    Powell, AA
    Gause, PR
    Craven, MT
    Payne, CM
    Powell, MB
    Gerner, EW
    Earnest, DL
    NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL, 1998, 31 (02): : 111 - 118
  • [36] Bile Acids and Metabolic Regulation Mechanisms and clinical responses to bile acid sequestration
    Staels, Bart
    Fonseca, Vivian A.
    DIABETES CARE, 2009, 32 : S237 - S245
  • [37] MORPHOLOGIC CHANGES IN LIVERS OF HAMSTERS TREATED WITH HIGH-DOSES OF URSODEOXYCHOLIC ACID - CORRELATION WITH BILE-ACIDS IN BILE
    MAMIANETTI, A
    KONOPKA, HF
    LAGO, N
    VESCINA, C
    SCARLATO, E
    CARDUCCI, CN
    PHARMACOLOGICAL RESEARCH, 1994, 29 (02) : 187 - 195
  • [38] URSODEOXYCHOLIC ACID, 7-KETOLITHOCHOLIC ACID, AND CHENODEOXYCHOLIC ACID ARE PRIMARY BILE-ACIDS OF THE NUTRIA (MYOCASTOR, COYPUS)
    TINT, GS
    BULLOCK, J
    BATTA, AK
    SHEFER, S
    SALEN, G
    GASTROENTEROLOGY, 1986, 90 (03) : 702 - 709
  • [39] URSODEOXYCHOLIC ACID ENHANCES BILE CANALICULAR CONTRACTIONS
    ODA, M
    YOKOMORI, M
    ISHII, K
    NISHIZAKI, Y
    INOUE, J
    WATANABE, N
    TSUCHIYA, M
    HEPATOLOGY, 1990, 12 (04) : 999 - 999
  • [40] URSODEOXYCHOLIC ACID, CHENODEOXYCHOLIC ACID, AND 7-KETOLITHOCHOLIC ACID ARE PRIMARY BILE-ACIDS OF THE GUINEA-PIG
    TINT, GS
    XU, GR
    BATTA, AK
    SHEFER, S
    NIEMANN, W
    SALEN, G
    JOURNAL OF LIPID RESEARCH, 1990, 31 (07) : 1301 - 1306