Literature DB >> 4834548

The control of bile acid pool size: effect of jejunal resection and phenobarbitone on bile acid metabolism in the rat.

H Y Mok, P M Perry, R H Dowling.   

Abstract

In patients with cholesterol gallstones, there is a diminished bile acid pool and the bile becomes supersaturated with cholesterol. Medical treatment has been aimed at re-expanding the pool to improve cholesterol solubility in bile but as yet the factors controlling the size of the bile acid pool' are unknown. Therefore the role of the liver and intestine in controlling bile acid pool size in the rat was studied and the effect of experimental expansion of the pool on bile acid metabolism and bile lipid composition examined. Bile acid absorption was increased from ileum made hyperplastic by previous jejunectomy and hepatic bile acid synthesis was increased by phenobarbitone treatment. Both jejunal resection and phenobarbitone significantly increased the size of the bile acid pool from 32.2 +/- SEM 0.94 mumoles/100 g body weight to 42.2 +/- 1.71 and 44.4 +/- 2.03 respectively. However, the effects of these experimental manipulations on bile acid secretion rate, enterohepatic cycling frequency, and synthesis rates were quite different. Jejunectomy caused a 56% increase in bile acid secretion and more rapid cycling of the bile acid pool but the enhanced absorption did not depress bile acid synthesis. In contrast, phenobarbitone markedly increased synthesis from 14.5 +/- 1.42 mumoles.100 g BW(-1). 24 hr(-1) to 25.9 +/- 3.19 but there was no significant change in bile acid secretion and the choleresis seen after phenobarbitone was mainly due to an increase in the bile acid-independent fraction of bile flow. In these experimental studies in the rat, expansion of the bile acid pool did not significantly change bile lipid composition or cholesterol solubility in bile.

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Year:  1974        PMID: 4834548      PMCID: PMC1412956     

Source DB:  PubMed          Journal:  Gut        ISSN: 0017-5749            Impact factor:   23.059


  39 in total

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Authors:  R H Dowling; E Mack; J Picott; J Berger; D M Small
Journal:  J Lab Clin Med       Date:  1968-07

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Authors:  S Nilsson; T Scherstén
Journal:  Gastroenterology       Date:  1969-11       Impact factor: 22.682

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Journal:  Eur J Biochem       Date:  1968-11

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Authors:  S Erlinger; D Dhumeaux; J P Benhamou; R Fauvert
Journal:  Rev Fr Etud Clin Biol       Date:  1969-02

5.  Structural and functional changes following small intestinal resection in the rat.

Authors:  R H Dowling; C C Booth
Journal:  Clin Sci       Date:  1967-02       Impact factor: 6.124

6.  Effect of phenobarbital on the excretion of an exogenous bilirubin load.

Authors:  R J Roberts; G L Plaa
Journal:  Biochem Pharmacol       Date:  1967-05       Impact factor: 5.858

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Authors:  S Shefer; S Hauser; E H Mosbach
Journal:  J Lipid Res       Date:  1968-05       Impact factor: 5.922

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Authors:  W H Admirand; D M Small
Journal:  J Clin Invest       Date:  1968-05       Impact factor: 14.808

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Authors:  H P Schedl; C E Pierce; A Rider; J A Clifton
Journal:  J Clin Invest       Date:  1968-02       Impact factor: 14.808

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Journal:  J Cell Biol       Date:  1969-07       Impact factor: 10.539

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  13 in total

1.  Equilibrium-dialysis studies of the interaction between cholic acid and 100000g-supernatant preparations from the rat liver.

Authors:  R C Strange; I A Nimmo; I W Percy-Robb
Journal:  Biochem J       Date:  1976-05-15       Impact factor: 3.857

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Journal:  Gut       Date:  1974-11       Impact factor: 23.059

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Journal:  Lipids       Date:  1978-01       Impact factor: 1.880

5.  The effects of 3,5,5-trimethylcyclohexanol on hepatic cholesterol synthesis, bile flow and biliary lipid secretion in the rat.

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Journal:  Br J Pharmacol       Date:  1984-01       Impact factor: 8.739

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Journal:  Br Med J       Date:  1978-06-10

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Authors:  Clavia Ruth Wooton-Kee; David E Cohen; Mary Vore
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2008-02-21       Impact factor: 4.052

8.  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

9.  Physiologic study of bile salt and lipid secretion in rats after liver transplantation.

Authors:  H S Xu; J A Pilcher; R S Jones
Journal:  Ann Surg       Date:  1993-04       Impact factor: 12.969

10.  Regulation of bile salt transport in rat liver. Evidence that increased maximum bile salt secretory capacity is due to increased cholic acid receptors.

Authors:  F R Simon; E M Sutherland; M Gonzalez
Journal:  J Clin Invest       Date:  1982-08       Impact factor: 14.808

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