Oxidative stress and apoptosis in fetal rat liver induced by maternal cholestasis. Protective effect of ursodeoxycholic acid

被引:67
作者
Perez, MJ
Macias, RIR
Duran, C
Monte, MJ
Gonzalez-Buitrago, JM
Marin, JJG
机构
[1] Univ Salamanca, Dept Physiol & Pharmacol, Lab Expt Hepatol & Drug Targeting, Salamanca 37007, Spain
[2] Univ Salamanca, Univ Hosp, Lab Expt Hepatol & Drug Targeting, Salamanca 37007, Spain
关键词
bax; bile acid; caspase; glutathione; pregnancy;
D O I
10.1016/j.jhep.2005.02.028
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: The sensitivity of fetal rat liver to maternal obstructive cholestasis during pregnancy (OCP), and the effect of ursodeoxycholic acid (UDCA) were investigated. Methods: UDCA was administered (i.g. 0.6 mg/kg b.wt./day) from day 14 to day 21 of pregnancy after maternal common bile duct ligation. Results: Impairment in the activity of antioxidant enzymes, levels of total glutathione and GSH/GSSG ratio and the degrees of lipid peroxidation and protein carbonylation were similar in livers of OCP mothers and fetuses at term, despite hypercholanemia was milder in fetuses. Treatment of OCP rats with UDCA reduced maternal and fetal liver oxidative stress. Although maternal hypercholanemia was not corrected, fetal serum concentrations of major bile acids (except UDCA and beta-muricholic acid) were reduced. Fetal liver expression of key enzyme in bile acid synthesis, Cyp7a1, Cyp27 and Cyp8b1 was not affected by OCP or UDCA treatment. In OCP fetal livers, the relative expression of Bax-alpha: and Bcl-2 and the activity of caspase-3, but not caspase-8, were increased. These changes were markedly reduced in fetuses of OCP animals treated with UDCA. Conclusions: OCP induced moderate fetal hypercholanemia but marked liver oxidative stress and apoptosis that were partly prevented by treatment of pregnant rats with UDCA. (c) 2005 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
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页码:324 / 332
页数:9
相关论文
共 51 条
[1]  
[Anonymous], FRONT BIOSCI
[2]   BILE ACID-INDUCED LIVER TOXICITY - RELATION TO THE HYDROPHOBICHYDROPHILIC BALANCE OF BILE-ACIDS [J].
ATTILI, AF ;
ANGELICO, M ;
CANTAFORA, A ;
ALVARO, D ;
CAPOCACCIA, L .
MEDICAL HYPOTHESES, 1986, 19 (01) :57-69
[3]   EFFECTS OF BILE-SALTS ON THE PLASMA-MEMBRANES OF ISOLATED RAT HEPATOCYTES [J].
BILLINGTON, D ;
EVANS, CE ;
GODFREY, PP ;
COLEMAN, R .
BIOCHEMICAL JOURNAL, 1980, 188 (02) :321-327
[4]   Usefulness of liposomes loaded with cytostatic bile acid derivatives to circumvent chemotherapy resistance of enterohepatic tumors [J].
Briz, O ;
Macias, RIR ;
Vallejo, M ;
Silva, A ;
Serrano, MA ;
Marin, JJG .
MOLECULAR PHARMACOLOGY, 2003, 63 (03) :742-750
[5]  
CARLBERG I, 1985, METHOD ENZYMOL, V113, P484
[6]  
CLAIBORNE A, 1979, J BIOL CHEM, V254, P4245
[7]   Induction and regulation of hepatocyte apoptosis by oxidative stress [J].
Czaja, MJ .
ANTIOXIDANTS & REDOX SIGNALING, 2002, 4 (05) :759-767
[8]  
DUMONT M, 1980, GASTROENTEROLOGY, V79, P82
[9]  
ElMir MY, 1997, HEPATOLOGY, V26, P527, DOI 10.1002/hep.510260301
[10]   Toxic bile salts induce rodent hepatocyte apoptosis via direct activation of Fas [J].
Faubion, WA ;
Guicciardi, ME ;
Miyoshi, H ;
Bronk, SF ;
Roberts, PJ ;
Svingen, PA ;
Kaufmann, SH ;
Gores, GJ .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (01) :137-145