Literature DB >> 16125

Possible explanations for the differences in secretory characteristics between conjugated and free bile acids.

E R O'Máille, T G Richards.   

Abstract

1. The hepatic extraction fraction and maximum excretory rate of conjugated cholate are greater than those of free cholate (studied after acute taurine depletion); the possibility that this difference might be due to greater bile-to-blood back-diffusion of un-ionized cholic acid (pKa 5-5) compared to that of taurocholic acid (pKa 2) has been investigated by varying the pH of bile by secretin or acetazolamide administration in the anaesthetized dog. 2. The mean biliary pH during free cholate excretion in the control state in twenty-three experiments was 7-5 (at which approximately 1% of cholate is un-ionized). Three to fourfold changes in the hydrogen ion activity of bile (which resulted in changes of the same magnitude in the percentage of un-ionized cholic acid) had no significant effect on the total (mainly free) cholate maximum excretory rate. It is concluded that back-diffusion of un-ionized cholic acid in the bile ducts is not an important determinant of the secretory performance of free cholate. 3. The bile flow rate associated with mainly free cholate excretion is much higher than that associated with taurocholate excretion at the same rate; the extra bile flow appears to arise largely by means that are independent of the osmotic effect of cholate excretion, as the osmotic coefficient (osmolality/total solute concentration) of bile containing mainly free free cholate (calculated directly) was only slightly greater than that of bile containing mainly taurocholate (obtained by extrapolation) at the same total cholate concentration. 4. The peak hepatic excretory rate of taurocholate following the instillation of the entire contents of the gall-bladder of a fasted dog into the distal ileum was only about one fifth of the maximum rate attainable; at the peak rate taurocholate is almost completely removed in the first passage of blood through the liver.

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Year:  1977        PMID: 16125      PMCID: PMC1307852          DOI: 10.1113/jphysiol.1977.sp011748

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  14 in total

Review 1.  Secretion of bile acids by the liver and their role in the formation of hepatic bile.

Authors:  H O Wheeler
Journal:  Arch Intern Med       Date:  1972-10

2.  [On the absorption inhibiting effect of bile acids].

Authors:  W Forth; W Rummel; H Glasner
Journal:  Naunyn Schmiedebergs Arch Pharmakol Exp Pathol       Date:  1966

3.  Lipase and bile salts in the small intestine of the dog. Relation to lipid absorption.

Authors:  R Kiekens; P Wissocq; J P Govaerts
Journal:  Digestion       Date:  1971       Impact factor: 3.216

4.  Canalicular bile production in dogs.

Authors:  H O Wheeler; E D Ross; S E Bradley
Journal:  Am J Physiol       Date:  1968-04

5.  Effect on bile formation of inhibitors of sodium transport.

Authors:  S Erlinger; D Dhumeaux; J P Benhamou
Journal:  Nature       Date:  1969-09-20       Impact factor: 49.962

6.  Observations on the elimination rates of single injections of taurocholate and cholate in the dog.

Authors:  E R O'Máille; T G Richards; A H Short
Journal:  Q J Exp Physiol Cogn Med Sci       Date:  1969-07

7.  Bile acid metabolism. I. Studies on the mechanisms of intestinal transport.

Authors:  J M Dietschy; H S Salomon; M D Siperstein
Journal:  J Clin Invest       Date:  1966-06       Impact factor: 14.808

8.  Acute taurine depletion and maximal rates of hepatic conjugation and secretion of cholic acid in the dog.

Authors:  E R O'Máille; T G Richards; A H Short
Journal:  J Physiol       Date:  1965-09       Impact factor: 5.182

9.  Species differences in cholesterol-complexing macromolecular fractions in bile in relation to gallstone formation.

Authors:  F Nakayama; H Miyake
Journal:  J Lab Clin Med       Date:  1966-01

10.  Characterization of the kinetics of the passive and active transport mechanisms for bile acid absorption in the small intestine and colon of the rat.

Authors:  E R Schiff; N C Small; J M Dietschy
Journal:  J Clin Invest       Date:  1972-06       Impact factor: 14.808

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  3 in total

1.  Bile salt secretion.

Authors:  E R O'Máille
Journal:  Ir J Med Sci       Date:  1977-07       Impact factor: 1.568

2.  Hypercholeresis with cholate infusion in dogs with pigment gallstones.

Authors:  J Matsumura; K Neri; R V Rege
Journal:  Dig Dis Sci       Date:  1996-02       Impact factor: 3.199

3.  The influence of micelle formation on bile salt secretion.

Authors:  E R O'Máille
Journal:  J Physiol       Date:  1980-05       Impact factor: 5.182

  3 in total

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