Literature DB >> 4385432

Formation of bile acids in man: conversion of cholesterol into 5-beta-cholestane-3-alpha, 7-alpha, 12-alpha-triol in liver homogenates.

I Björkheim, H Danielsson, K Einarsson, G Johansson.   

Abstract

The mechanisms of the conversion of cholesterol into bile acids in man were studied by examining the metabolism of cholesterol-1,2-(3)H, cholest-5-ene-3beta,7alpha-diol-7beta-(3)H, tritiumlabeled 7alpha-hydroxycholest-4-en-3-one, 7alpha,12alpha-dihydroxycholest-4-en-3-one, and cholest-5-ene-3beta,7alpha,12alpha-triol in fractions of liver homogenates. The 20,000 g supernatant fluid catalyzed the conversion of cholesterol into cholest-5-ene-3beta,7alpha-diol, 7alpha-hydroxycholest-4-en-3-one, 7alpha-12alpha-dihydroxycholest-4-en-3-one, and 5beta-cholestane-3alpha,7alpha,12alpha-triol. In the presence of microsomal fraction fortified with NAD(+), cholest-5-ene-3beta,7alpha-diol was converted into 7alpha-hydroxycholest-4-en-3-one, and when this fraction was fortified with NADPH small amounts of cholest-5-ene-3beta-7alpha,12alpha-triol were formed. 7alpha-Hydroxycholest-4-en-3-one was metabolized into 7alpha-12alpha-dihydroxycholest-4-en-3-one in the presence of microsomal fraction fortified with NADPH and into 5beta-cholestane-3alpha,7alpha-diol in the presence of 100,000 g supernatant fluid. Cholest-5-ene-3beta,7alpha,12alpha-triol was converted into 7alpha,12alpha-dihydroxycholest-4-en-3-one in the presence of microsomal fraction fortified with NAD(+). The 100,000 g supernatant fluid catalyzed the conversion of 7alpha,12alpha-dihydroxycholest-4-en-3-one into 5beta-cholestane-3alpha,7alpha,12alpha-triol. The sequence of reactions in the conversion of cholesterol into 5beta-cholestane-3alpha,7alpha-diol and 5beta-cholestane-3alpha,7alpha,12alpha-triol, the subcellular localization of the enzymes, and the cofactor requirements were found to be the same as those described for rat liver.

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Year:  1968        PMID: 4385432      PMCID: PMC297315          DOI: 10.1172/JCI105849

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  10 in total

1.  CONVERSION OF CHOLESTEROL TO TRIHYDROXYCOPROSTANIC ACID AND CHOLIC ACID IN MAN.

Authors:  J B CAREY
Journal:  J Clin Invest       Date:  1964-07       Impact factor: 14.808

2.  THE IN VITRO CATABOLISM OF CHOLESTEROL: FORMATION OF 3-ALPHA,7-ALPHA,12-ALPHA-TRIHYDROXYCOPROSTANE FROM CHOLESTEROL IN RAT LIVER.

Authors:  D MENDELSOHN; E STAPLE
Journal:  Biochemistry       Date:  1963 May-Jun       Impact factor: 3.162

3.  Formation of trihydroxycoprostanic acid from cholesterol in man.

Authors:  E STAPLE; J L RABINOWITZ
Journal:  Biochim Biophys Acta       Date:  1962-06-04

4.  Synthesis and metabolism of cholest-5-ene-3 beta, 7-alpha, 12-alpha-triol.

Authors:  O Berséus; H Danielsson; K Einarsson
Journal:  J Biol Chem       Date:  1967-03-25       Impact factor: 5.157

5.  On the conversion of cholesterol to 7-alpha,12-alpha-dihydroxycholest-4-en-3-one. Bile acids and steroids 168.

Authors:  H Danielsson; K Einarsson
Journal:  J Biol Chem       Date:  1966-04-10       Impact factor: 5.157

6.  The metabolism of cholest-5-en-3-beta, 7-alpha-diol by rat-liver cell fractions.

Authors:  H R Hutton; G S Boyd
Journal:  Biochim Biophys Acta       Date:  1966-04-04

7.  The in vitro catabolism of cholesterol: a comparison of the formation of cholest-4-en-7-alpha-ol-3-one and 5-beta-cholestan-7-alpha-ol-3-one from cholesterol in rat liver.

Authors:  D Mendelsohn; L Mendelsohn; E Staple
Journal:  Biochemistry       Date:  1966-04       Impact factor: 3.162

8.  On the synthesis and metabolism of cholest-4-en-7-alpha-ol-3-one. Bile acids and steroids 156.

Authors:  I Björkhem; H Danielsson; C Issidorides; A Kallner
Journal:  Acta Chem Scand       Date:  1965

9.  On the conversion of cholesterol to 5-beta-cholestane-3-alpha, 7-alpha-diol in guinea pig liver homogenates.

Authors:  I Björkhem; H Danielsson; K Einarsson
Journal:  Eur J Biochem       Date:  1967-10

10.  SYNTHESIS AND METABOLISM OF CHOLEST-4-ENE-7-ALPHA,12-ALPHA-DIOL-3-ONE AND 5-BETA-CHOLESTANE-7-ALPHA,12-ALPHA-DIOL-3-ONE. BILE ACIDS AND STEROIDS 153.

Authors:  O BERSEUS; H DANIELSSON; A KALLNER
Journal:  J Biol Chem       Date:  1965-06       Impact factor: 5.157

  10 in total
  8 in total

1.  Normal antipyrine metabolism in patients with cholesterol cholelithiasis. Evidence that the disease is not due to generalized hepatic microsomal dysfunction.

Authors:  G W Hepner; E S Vesell
Journal:  Am J Dig Dis       Date:  1975-01

2.  Effects of clofibrate on some microsomal hydroxylations involved in the formation and metabolism of bile acids in rat liver.

Authors:  B O Angelin; I Björkhem; K Einarsson
Journal:  Biochem J       Date:  1976-05-15       Impact factor: 3.857

3.  Human and murine steroid 5β-reductases (AKR1D1 and AKR1D4): insights into the role of the catalytic glutamic acid.

Authors:  Mo Chen; Phumvadee Wangtrakuldee; Tianzhu Zang; Ling Duan; Laura L Gathercole; Jeremy W Tomlinson; Trevor M Penning
Journal:  Chem Biol Interact       Date:  2019-03-28       Impact factor: 5.192

4.  Biosynthesis of bile acids in man. Hydroxylation of the C27-steroid side chain.

Authors:  I Björkhem; J Gustafsson; G Johansson; B Persson
Journal:  J Clin Invest       Date:  1975-03       Impact factor: 14.808

5.  Biosynthesis of chenodeoxycholic acid in man: stereospecific side-chain hydroxylations of 5beta-cholestane-3alpha,7alpha-diol.

Authors:  S Shefer; F W Cheng; A K Batta; B Dayal; G S Tint; G Salen
Journal:  J Clin Invest       Date:  1978-09       Impact factor: 14.808

6.  Bile acid synthesis in man: metabolism of 7 -hydroxycholesterol- 14 C and 26-hydroxycholesterol- 3 H.

Authors:  K E Anderson; E Kok; N B Javitt
Journal:  J Clin Invest       Date:  1972-01       Impact factor: 14.808

7.  Cerebrotendinous xanthomatosis: a defect in mitochondrial 26-hydroxylation required for normal biosynthesis of cholic acid.

Authors:  H Oftebro; I Björkhem; S Skrede; A Schreiner; J I Pederson
Journal:  J Clin Invest       Date:  1980-06       Impact factor: 14.808

8.  In vivo and vitro studies on formation of bile acids in patients with Zellweger syndrome. Evidence that peroxisomes are of importance in the normal biosynthesis of both cholic and chenodeoxycholic acid.

Authors:  B F Kase; J I Pedersen; B Strandvik; I Björkhem
Journal:  J Clin Invest       Date:  1985-12       Impact factor: 14.808

  8 in total

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