Literature DB >> 1163658

Hepatic bile acid transport: effect of conjugation and position of hydroxyl groups.

N E Hoffman, J H Iser, R A Smallwood.   

Abstract

The hepatic transport of five bile acids was studied in the bile-fistula rat. Pairs of labeled bile acids were injected simultaneously into the portal vein as a sharp pulse and the secretion of radiolabel in bile was measured over the nex 15 min. Six bile acid pairs were tested, and it was found that both conjugation and the number and disposition of hydroxyl groups influenced hepatic transport. Taurocholic acid was transported most efficiently, followed in order by glycocholic acid, cholic acid, deoxycholic acid, and chenodeoxycholic acid. Sampling aortic blood immediately after portal vein injection of labeled bile acid pairs demonstrated differential rates of hepatic extraction. In every comparison, the bile acid that was more efficiently extracted by the liver had a faster overall transport rate. This suggests that the differing rates of biliary secretion are, at least in part, determined by the efficiency of hepatic uptake.

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Year:  1975        PMID: 1163658     DOI: 10.1152/ajplegacy.1975.229.2.298

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


  15 in total

Review 1.  Enterohepatic circulation: physiological, pharmacokinetic and clinical implications.

Authors:  Michael S Roberts; Beatrice M Magnusson; Frank J Burczynski; Michael Weiss
Journal:  Clin Pharmacokinet       Date:  2002       Impact factor: 6.447

2.  Residence time distributions of solutes in the perfused rat liver using a dispersion model of hepatic elimination: 1. Effect of changes in perfusate flow and albumin concentration on sucrose and taurocholate.

Authors:  M S Roberts; S Fraser; A Wagner; L McLeod
Journal:  J Pharmacokinet Biopharm       Date:  1990-06

Review 3.  Biochemistry of bile secretion.

Authors:  R Coleman
Journal:  Biochem J       Date:  1987-06-01       Impact factor: 3.857

4.  Plasma clearance of oral and intravenous cholic acid in subjects with and without chronic liver disease.

Authors:  I T Gilmore; R P Thompson
Journal:  Gut       Date:  1980-02       Impact factor: 23.059

5.  Differential disposition of chenodeoxycholic acid versus taurocholic acid in response to acute troglitazone exposure in rat hepatocytes.

Authors:  Tracy L Marion; Cassandra H Perry; Robert L St Claire; Wei Yue; Kim L R Brouwer
Journal:  Toxicol Sci       Date:  2011-01-24       Impact factor: 4.849

6.  Kinetics of 14C-glycocholic acid clearance in normal man and in patients with liver disease.

Authors:  I T Gilmore; R P Thompson
Journal:  Gut       Date:  1978-12       Impact factor: 23.059

Review 7.  Taurine and the renal system.

Authors:  Russell W Chesney; Xiaobin Han; Andrea B Patters
Journal:  J Biomed Sci       Date:  2010-08-24       Impact factor: 8.410

8.  Bile acid conjugation in the chimpanzee: effective sulfation of lithocholic acid.

Authors:  M Schwenk; A F Hofmann; G L Carlson; J A Carter; F Coulston; H Greim
Journal:  Arch Toxicol       Date:  1978-04-27       Impact factor: 5.153

9.  Pharmacokinetics and biliary excretion of bromosulphophthalein, [3H]-ouabain and [3H]-taurocholic acid in rats with glycerol-induced acute renal failure.

Authors:  C J Bowmer; M S Yates
Journal:  Br J Pharmacol       Date:  1984-11       Impact factor: 8.739

Review 10.  Chenodeoxycholic acid: a review of its pharmacological properties and therapeutic use.

Authors:  J H Iser; A Sali
Journal:  Drugs       Date:  1981-02       Impact factor: 9.546

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