Literature DB >> 9374698

Enterohepatic circulation of scymnol sulfate in an elasmobranch, the little skate (Raja erinacea).

G Fricker1, R Wössner, J Drewe, R Fricker, J L Boyer.   

Abstract

The sulfated bile alcohol scymnol sulfate (ScyS), 3 alpha,7 alpha,12 alpha,24 xi, 26,27-hexahydroxy-5 beta-cholestane-26(27)-sulfate, is the major bile salt in bile of an elasmobranch, the little skate. To investigate hepatic transport of bile alcohols in skate liver, [3H]ScyS and a potential precursor, 3 alpha,7 alpha,12 alpha-trihydroxy-5 beta-cholestane (chtriol), were used as model compounds. Their transport into isolated hepatocytes was partially saturable, temperature sensitive, and Na+ independent. The uptake of ScyS was inhibited by cholyltaurine, and uptake of cholyltaurine was inhibited by ScyS in a competitive manner. In contrast, uptake of chtriol was not inhibited by cholyltaurine, suggesting separate transport systems. ScyS and chtriol showed a choleretic effect in isolated perfused livers. When ScyS was added to the perfusate of isolated perfused livers, > 25% was found in bile within 7 h. When chtriol was added to the perfusate, 10% of the dose was secreted into the bile mainly in the form of polar metabolites, whereas only nonmetabolized chtriol remained in the livers. The slow bile flow of 40-50 microliters/h and the high recovery in the liver suggest that metabolism may be the rate-limiting step in the hepatic elimination of chtriol. The major metabolites secreted into bile were identified by mass spectrometry and chromatography as scymnol and ScyS. To study the enterohepatic circulation, [3H]ScyS or [3H]chtriol was administered into the duodenum of free-swimming skates, and bile was collected through exteriorized indwelling cannulas over a 4-day period. More than 90% of the radioactivity was recovered from bile, indicating that there was a highly effective absorption in the intestinal epithelium, as well as specific transport mechanisms for hepatic uptake and biliary secretion of these compounds. This is the first direct demonstration of an enterohepatic circulation for a bile alcohol sulfate in fish liver.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9374698     DOI: 10.1152/ajpgi.1997.273.5.G1023

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  6 in total

1.  Expression cloning of two genes that together mediate organic solute and steroid transport in the liver of a marine vertebrate.

Authors:  W Wang; D J Seward; L Li; J L Boyer; N Ballatori
Journal:  Proc Natl Acad Sci U S A       Date:  2001-07-24       Impact factor: 11.205

2.  Evidence that petromyzontid lampreys employ a common migratory pheromone that is partially comprised of bile acids.

Authors:  Jared M Fine; Lance A Vrieze; Peter W Sorensen
Journal:  J Chem Ecol       Date:  2004-11       Impact factor: 2.626

Review 3.  Assessing the bioaccumulation potential of ionizable organic compounds: Current knowledge and research priorities.

Authors:  James M Armitage; Russell J Erickson; Till Luckenbach; Carla A Ng; Ryan S Prosser; Jon A Arnot; Kristin Schirmer; John W Nichols
Journal:  Environ Toxicol Chem       Date:  2016-12-19       Impact factor: 3.742

4.  Hepatic uptake and biliary excretion of manganese in the little skate, Leucoraja erinacea.

Authors:  Michael S Madejczyk; James L Boyer; Nazzareno Ballatori
Journal:  Comp Biochem Physiol C Toxicol Pharmacol       Date:  2008-12-24       Impact factor: 3.228

5.  Not all (bile acids) who wander are lost: the first report of a patient with an isolated NTCP defect.

Authors:  Saul J Karpen; Paul A Dawson
Journal:  Hepatology       Date:  2014-11-20       Impact factor: 17.425

6.  Evolution of substrate specificity for the bile salt transporter ASBT (SLC10A2).

Authors:  Daniël A Lionarons; James L Boyer; Shi-Ying Cai
Journal:  J Lipid Res       Date:  2012-06-05       Impact factor: 5.922

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.