Literature DB >> 7109494

Phenobarbital-induced alterations of bile acid metabolism in cases of intrahepatic cholestasis.

P Back.   

Abstract

Bile acid profiles from plasma and urine of six patients suffering from intrahepatic cholestasis were studied before and during treatment with phenobarbital. All patients responded to this treatment by decreasing their plasma bile acid levels. Using gas chromatographic and mass spectrometric methods for separation and identification of the bile acids, especially the occurrence of major atypical bile acids was quantitatively evaluated. The plasma bile acid lowering effect of phenobarbital in intrahepatic cholestasis can be partly explained by an increased formation of tetrahydroxylated bile acids, which are rapidly excreted by renal pathways. These tetrahydroxylated bile acids, present as nonsulfated compounds, have high renal excretory flow rates exceeding those of bile acid sulfates. Their enterohepatic circulation, however, seems to be low, since only small amounts of tetrahydroxylated bile acids can be found in bile. It is mainly the 1- and 6-hydroxylation that is stimulated by phenobarbital. The exact site of formation of tetrahydroxylated bile acids, however, is still unknown. These findings may provide a rationale for the institution of a phenobarbital treatment in cases of intrahepatic cholestasis.

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Year:  1982        PMID: 7109494     DOI: 10.1007/BF01724209

Source DB:  PubMed          Journal:  Klin Wochenschr        ISSN: 0023-2173


  25 in total

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Authors:  K Einarsson; G Johansson
Journal:  FEBS Lett       Date:  1969-08       Impact factor: 4.124

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Journal:  Eur J Clin Invest       Date:  1979-10       Impact factor: 4.686

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Journal:  J Lipid Res       Date:  1963-01       Impact factor: 5.922

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Authors:  V S Ostrower; P Coan; F Kern
Journal:  Gastroenterology       Date:  1974-12       Impact factor: 22.682

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Authors:  A Stiehl; M M Thaler; W H Admirand
Journal:  Pediatrics       Date:  1973-06       Impact factor: 7.124

6.  Bile acids and their sulphated and glucuronidated derivatives in bile, plasma, and urine of children with intrahepatic cholestasis: effects of phenobarbital treatment.

Authors:  A Stiehl; M Becker; P Czygan; W Fröhling; B Kommerell; H W Rotthauwe; M Senn
Journal:  Eur J Clin Invest       Date:  1980-08       Impact factor: 4.686

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Authors:  P Back; K Walter
Journal:  Gastroenterology       Date:  1980-04       Impact factor: 22.682

8.  Induction of UDPglucose dehydrogenase during development, organ culture, and exposure to phenobarbital. Its relation to levels of UDPglucuronic acid and overall glucuronidation in chicken and mouse.

Authors:  J Fyffe; G J Dutton
Journal:  Biochim Biophys Acta       Date:  1975-11-10

9.  Steroid metabolism in rats given (1- 2 H 2 )ethanol. Oxidoreduction of isomeric 3-hydroxycholanoic acids and reduction of 3-oxo-4-cholenoic acid.

Authors:  T Cronholm; I Makino; J Sjövall
Journal:  Eur J Biochem       Date:  1972-03-27

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Authors:  A Bremmelgaard; J Sjövall
Journal:  J Lipid Res       Date:  1980-11       Impact factor: 5.922

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  8 in total

Review 1.  Phenotyping of Human CYP450 Enzymes by Endobiotics: Current Knowledge and Methodological Approaches.

Authors:  Gaëlle Magliocco; Aurélien Thomas; Jules Desmeules; Youssef Daali
Journal:  Clin Pharmacokinet       Date:  2019-11       Impact factor: 6.447

2.  Prognostic roles of tetrahydroxy bile acids in infantile intrahepatic cholestasis.

Authors:  Chee-Seng Lee; Akihiko Kimura; Jia-Feng Wu; Yen-Hsuan Ni; Hong-Yuan Hsu; Mei-Hwei Chang; Hiroshi Nittono; Huey-Ling Chen
Journal:  J Lipid Res       Date:  2017-01-10       Impact factor: 5.922

3.  Effect of rifampicin treatment on hepatic drug metabolism and serum bile acids in patients with primary biliary cirrhosis.

Authors:  H P Hoensch; K Balzer; P Dylewizc; W Kirch; H Goebell; E E Ohnhaus
Journal:  Eur J Clin Pharmacol       Date:  1985       Impact factor: 2.953

4.  Glucuronidation of 6 alpha-hydroxy bile acids by human liver microsomes.

Authors:  A Radomińska-Pyrek; P Zimniak; Y M Irshaid; R Lester; T R Tephly; J St Pyrek
Journal:  J Clin Invest       Date:  1987-07       Impact factor: 14.808

5.  Studies on the mechanism of 1-(2-chloroethyl)-3-cyclohexyl-1-nitrosourea (CCNU)-induced hepatotoxicity. II. Biochemical and morphological characterization of the injury and its prevention by phenobarbital.

Authors:  A E Ahmed; M Grissom; R el-Azhary; A Haque; P J Boor; J Costanzi
Journal:  Cancer Chemother Pharmacol       Date:  1987       Impact factor: 3.333

6.  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

7.  Effects of phenobarbital on biliary lipid metabolism in children with chronic intrahepatic cholestasis.

Authors:  M Becker; K von Bergmann; H W Rotthauwe; O Leiss
Journal:  Eur J Pediatr       Date:  1984-11       Impact factor: 3.183

8.  Plasma bile acids in patients with peroxisomal dysfunction syndromes: analysis by capillary gas chromatography-mass spectrometry.

Authors:  P T Clayton; B D Lake; N A Hall; D B Shortland; R A Carruthers; A M Lawson
Journal:  Eur J Pediatr       Date:  1987-03       Impact factor: 3.183

  8 in total

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