Literature DB >> 631488

Pool size, synthesis, and turnover of sulfated and nonsulfated cholic acid and chenodeoxycholic acid in patients with cirrhosis of the liver.

A Stiehl, E Ast, P Czygan, W Fröhling, R Raedsch, B Kommerell.   

Abstract

In 5 patients with cirrhosis of the liver sulfated and nonsulfated [14C]cholic acid and [14C]chenodeoxycholic acid were administered intravenously and the specific activity curves were determined. Specific activities declined exponentially and pool sizes, synthesis rates, and turnover rates of bile acids were calculated on the basis of a one-pool system. The biological half-life of cholic acid was 4.3 +/- 1.6 days (mean +/- SEM) and of chenodeoxycholic acid was 2.8 +/- 1.2 days. The half-life of cholic acid sulfate was 0.7 +/- 0.5 day and of chenodeoxycholic acid sulfate was 0.8 +/- 0.5 day. The pool size of cholic acid was 513 +/- 103 mg, of chenodeoxycholic acid, 477 +/- 77 mg, of cholic acid sulfate, 4.7 +/- 1.0 mg, and of chenodeoxycholic acid sulfate, 38.7 +/- 4.0 mg. The daily synthesis of cholic acid was 90 +/- 14 mg, of chenodeoxycholic acid, 118 +/- 6 mg, of cholic acid sulfate, 7.2 +/- 2.1 mg, and of chenodeoxycholic acid sulfate was 32.6 +/- 3.2 mg. The data indicate that sulfate esters of bile acids are significantly more rapidly excreted than are unsulfated bile acids. More than one-fourth of the chenodeoxycholic acid but less than one-tenth of the cholic acid formed was sulfated. The preferential sulfation of chenodeoxycholic acid is responsible for the more rapid turnover of chenodeoxycholic acid in comparison to cholic acid. Sulfation enhances the excretion and thereby prevents the accumulation of hepatotoxic concentrations of chenodeoxycholic acid in patients with cirrhosis of the liver.

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Year:  1978        PMID: 631488

Source DB:  PubMed          Journal:  Gastroenterology        ISSN: 0016-5085            Impact factor:   22.682


  7 in total

1.  Steatosis, cholestasis, and alkaline phosphatase in alcoholic liver disease.

Authors:  D B McGill
Journal:  Am J Dig Dis       Date:  1978-12

Review 2.  Clinical pharmacokinetics of therapeutic bile acids.

Authors:  A Crosignani; K D Setchell; P Invernizzi; A Larghi; C M Rodrigues; M Podda
Journal:  Clin Pharmacokinet       Date:  1996-05       Impact factor: 6.447

3.  Altered bile acid metabolism in primary biliary cirrhosis.

Authors:  R Raedsch; B H Lauterburg; A F Hofmann
Journal:  Dig Dis Sci       Date:  1981-05       Impact factor: 3.199

4.  [Pathogenic significance of bile acids (author's transl)].

Authors:  W Gerok; S Matern
Journal:  Klin Wochenschr       Date:  1981-06-15

5.  Prognostic significance of cholestatic alcoholic hepatitis. VA Cooperative Study Group #119.

Authors:  M Nissenbaum; A Chedid; C Mendenhall; P Gartside
Journal:  Dig Dis Sci       Date:  1990-07       Impact factor: 3.199

6.  Effect of chenodeoxycholic acid on the alterations of biliary lipid secretion induced by ethynylestradiol in the rat.

Authors:  P Bonazzi; G Novelli; R Galeazzi
Journal:  Br J Exp Pathol       Date:  1986-06

7.  Sulfated bile acids in serum, bile, and urine of cirrhotic patients before and after portacaval anastomosis.

Authors:  L Capocaccia; A F Attili; A Cantafora; F Bracci; L Paciscopi; C Puoti; U Pièche; M Angelico
Journal:  Dig Dis Sci       Date:  1981-06       Impact factor: 3.199

  7 in total

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