Literature DB >> 1150035

Metabolism of lethocholate in healthy man. I. Biotransformation and biliary excretion of intravenously administered lithocholate, lithocholylglycine, and their sulfates.

A E Cowen, M G Korman, A F Hofmann, O W Cass.   

Abstract

The metabolism of intravenously injected radiolabeled lithocholate, lithocholylglycine, and their 3alpha-sulfate esters was characterized in healthy subjects. Lithocholate radioactivity was excreted rapidly and predominantly in bile; the excreted radioactivity had the chromatographic properties of glycine and taurine conjugates of lithocholate, of which 60% were sulfated. Lithocholylglycine also was excreted rapidly and predominantly in bile, and 60% of excreted radioacitvity was sulfated. Sulfolithocholate radioactivity was only partially conjugated (about 60%) in association with biliary excretion. Sulfolithocholylglycine was excreted unchanged in bile. Neither sulfated derivative showed appreciable excretion in urine, although both were excreted more slowly in bile than unsulfated free or conjugated lithocholate. The data suggest that unconjugated lithocholate which is absorbed is completely conjugated and partially sulfated before excretion which occurs exclusively in bile. Since sulfation is not complete, some unsulfated lithocholate is always present in bile. This conjugated but unsulfated lithocholate, if reabsorbed, would be again partially sulfated during its next enterohepatic circulation. Thus, the end result of these biotransformations would be for absorbed lithocholate to be excreted in bile mostly, but not entirely as the sulfated conjugates.

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Year:  1975        PMID: 1150035

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


  30 in total

1.  Separate transport systems for biliary secretion of sulfated and unsulfated bile acids in the rat.

Authors:  F Kuipers; M Enserink; R Havinga; A B van der Steen; M J Hardonk; J Fevery; R J Vonk
Journal:  J Clin Invest       Date:  1988-05       Impact factor: 14.808

Review 2.  Cholesterol metabolism in man.

Authors:  S M Grundy
Journal:  West J Med       Date:  1978-01

3.  Will the real bile acid sulfotransferase please stand up? Identification of Sult2a8 as a major hepatic bile acid sulfonating enzyme in mice.

Authors:  Paul A Dawson; Kenneth D R Setchell
Journal:  J Lipid Res       Date:  2017-04-28       Impact factor: 5.922

Review 4.  Serum bile acids in hepatobiliary disease.

Authors:  I A Bouchier; C R Pennington
Journal:  Gut       Date:  1978-06       Impact factor: 23.059

5.  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

6.  Chenodeoxycholic acid induced liver injury in pregnant and neonatal baboons.

Authors:  C K McSherry; K P Morrissey; R L Swarm; P S May; W H Niemann; F Glenn
Journal:  Ann Surg       Date:  1976-10       Impact factor: 12.969

7.  Speed of change in biliary lipids and bile acids with chenodeoxycholic acid--is intermittent therapy feasible?

Authors:  J H Iser; G M Murphy; R H Dowling
Journal:  Gut       Date:  1977-01       Impact factor: 23.059

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.  Isolation of a bile salt sulfatase-producing Clostridium strain from rat intestinal microflora.

Authors:  S M Huijghebaert; J A Mertens; H J Eyssen
Journal:  Appl Environ Microbiol       Date:  1982-01       Impact factor: 4.792

10.  Sulphated bile acids in duodenal juice of healthy infants and children compared with sulphated bile acids in paediatric patients with various gastroenterological diseases.

Authors:  K H Niessen; M Teufel; G Brügmann
Journal:  Gut       Date:  1984-01       Impact factor: 23.059

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