Bile salt independent flow during bile salt-induced choleresis and cholestasis in the rat: role of biliary thiol secretion

被引:10
作者
Bouchard, G
Tuchweber, B
Yousef, IM
机构
[1] Univ Montreal, Dept Pharmacol, Montreal, PQ H3C 3J7, Canada
[2] Univ Montreal, Dept Nutr, Montreal, PQ H3C 3J7, Canada
[3] Hop St Justine, Ctr Rech Pediat, Montreal, PQ, Canada
来源
LIVER | 2000年 / 20卷 / 01期
关键词
bile acids; intrahepatic cholestasis; bile; glutathione; bile salt independent flow;
D O I
10.1034/j.1600-0676.2000.020001027.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Aims/Background: Previous studies have shown that the generation of the so-called "bile salt-independent flow" (BSIF) may be partly dependent on the hepatic availability and rate of canalicular secretion of osmotically active substances such as glutathione (GSH) and derived thiols, This study examined the role of common bile salts (BS) on the BSIF formation under both choleretic and cholestatic conditions, and on the relationship of the BSIF to the biliary thiol secretion. Methods: Experiments were carried out in adult male Sprague-Dawley rats both in situ in the isolated perfused rat liver and in vivo. The effect of choleretic and cholestatic doses of BS on the biliary BS secretion rate (BSSR), BS-dependent flow (BSDF), and BSIF was evaluated, Results. In the perfused rat liver, the infusion of low and physiological doses of taurocholic acid stimulated the biliary BSSR, BSDF, and BSIF This was associated with increased biliary thiol secretion and thiol-dependent bile flow. In vivo administration of taurocholic acid, taurochenodeoxycholic acid or taurolithocholic acid in step-wise increasing doses leading to cholestasis showed that the onset of cholestasis was not accompanied by a significant decline in the BSSR or BSDF but rather by a marked inhibition of the apparent BSIF During cholestasis, the three BS produced a significant reduction of biliary thiol secretion, with a marked decrease in thiol-dependent bile flow sufficient to account for a major proportion of BSIF inhibition. This decline in thiol secretion occurred before the drop in biliary BS secretion and was more pronounced than the reduction in BS output. No change in hepatic thiol content was observed. Administration of free or glycoconjugated BS also resulted in a significant decrease of BSIF during the cholestatic period, suggesting a common role for BSIF inhibition in BS-induced cholestasis. Conclusion. The changes in bile flow during BS-induced choleresis and cholestasis are mediated by changes in the portion of the BSIF regulated by the thiol secretion.
引用
收藏
页码:27 / 37
页数:11
相关论文
共 49 条
[1]   INTRAHEPATIC TRANSPORT AND UTILIZATION OF BILIARY GLUTATHIONE AND ITS METABOLITES [J].
ABBOTT, WA ;
MEISTER, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (05) :1246-1250
[2]  
BALABAUD C, 1977, J LAB CLIN MED, V89, P393
[3]   DETERMINANTS OF GLUTATHIONE EFFLUX AND BILIARY GSH GSSG RATIO IN PERFUSED RAT-LIVER [J].
BALLATORI, N ;
TRUONG, AT ;
MA, AK ;
BOYER, JL .
AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 256 (03) :G482-G490
[4]   GLUTATHIONE AS A PRIMARY OSMOTIC DRIVING FORCE IN HEPATIC BILE FORMATION [J].
BALLATORI, N ;
TRUONG, AT .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 263 (05) :G617-G624
[5]  
BALLATORI N, 1994, J BIOL CHEM, V269, P19731
[6]   RELATION BETWEEN BILIARY GLUTATHIONE EXCRETION AND BILE ACID-INDEPENDENT BILE-FLOW [J].
BALLATORI, N ;
TRUONG, AT .
AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 256 (01) :G22-G30
[7]  
BALLATORI N, 1990, MOL PHARMACOL, V38, P64
[8]   DECREASED BILIARY GLUTATHIONE CONTENT IS RESPONSIBLE FOR THE DECLINE IN BILE SALT-INDEPENDENT FLOW-INDUCED BY ETHINYL ESTRADIOL IN RATS [J].
BOUCHARD, G ;
YOUSEF, IM ;
TUCHWEBER, B .
TOXICOLOGY LETTERS, 1994, 74 (03) :221-233
[9]   URSODEOXYCHOLIC ACID INHIBITS GLUCAGON-INDUCED CAMP FORMATION IN HAMSTER HEPATOCYTES - A ROLE FOR PKC [J].
BOUSCAREL, B ;
GETTYS, TW ;
FROMM, H ;
DUBNER, H .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1995, 268 (02) :G300-G310
[10]  
BOYER J L, 1970, Journal of Clinical Investigation, V49, P206, DOI 10.1172/JCI106229