Literature DB >> 5972117

Factors determining the maximal rate of organic anion secretion by the liver and further evidence on the hepatic site of action of the hormone secretin.

E R O'Máille, T G Richards, A H Short.   

Abstract

1. Bromsulphthalein (BSP) was administered throughout the experiments at a constant rate well in excess of its excretory rate, to anaesthetized dogs in which the common bile duct had been cannulated. The maximal excretory rate of BSP into bile (BSP T(m)) obtained in this manner was greatly elevated by choleresis arising from the administration of bile salt (usually taurocholate) at constant rate.2. When bile flow rate was increased in stages by raising the taurocholate administration rate, successive increments in BSP excretion rate were obtained up to a limiting value of about 3 times the original T(m). Beyond this point further increases in taurocholate administration rate caused either no further enhancement of BSP T(m) or a decline in the extent of enhancement produced at a previous lower rate of infusion.3. When taurocholate maximal secretion was established first, the subsequent administration of BSP at progressively increasing rates led to reduction in the taurocholate secretion rate.4. Portal infusion of secretin at constant rate (usually 0.2 units/kg body wt. min) which caused substantial increases in bile flow rate, had no effect on BSP T(m). Increases of bile flow rate of the same order following constant taurocholate infusion produced marked elevation of the BSP T(m).5. These findings are discussed and the following conclusions reached:(a) The limiting factor in BSP maximal transfer is the concentration of BSP in bile; increased bile flow rate at the site of BSP excretion (canaliculi) produced by bile salt administration permits an increase in the original T(m) to occur without the limiting biliary concentration being exceeded.(b) There is excretory competition between BSP and bile salt but over a certain range of bile salt administration the facilitatory effects of increased bile flow rate outweigh the inhibitory effects due to competition.(c) Since secretin administration had no effect on BSP T(m), it is likely that the hydrocholeresis it produces originates downstream from the canaliculi, i.e. in the bile ductules or ducts; this supports previous evidence obtained in a different manner.

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Year:  1966        PMID: 5972117      PMCID: PMC1395860          DOI: 10.1113/jphysiol.1966.sp008044

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


  8 in total

1.  The activity of bile salts and certain detergents on the hepatic storage and protein-binding of sulphobromophthalein.

Authors:  W H ANDREWS; T G RICHARDS
Journal:  Q J Exp Physiol Cogn Med Sci       Date:  1960-07

2.  Biliary excretion of injected conjugated and unconjugated bilirubin by normal and Gunn rats.

Authors:  I M ARIAS; L JOHNSON; S WOLFSON
Journal:  Am J Physiol       Date:  1961-05

3.  Liver cell secretion under normal and pathologic conditions studied by fluorescence microscopy on living rats.

Authors:  V HANZON
Journal:  Acta Physiol Scand Suppl       Date:  1952

4.  The relationship between taurocholate secretion rate and bile production in the unanesthetized dog during cholinergic blockade and during secretin administration.

Authors:  R PREISIG; H L COOPER; H O WHEELER
Journal:  J Clin Invest       Date:  1962-05       Impact factor: 14.808

5.  On the preparation of secretin and pancreozymin.

Authors:  J CRICK; A A HARPER; H S RAPER
Journal:  J Physiol       Date:  1949-12       Impact factor: 5.182

6.  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

7.  Metabolism of sulfobromophthalein sodium (BSP) in dog and man.

Authors:  J I MELTZER; H O WHEELER; W I CRANSTON
Journal:  Proc Soc Exp Biol Med       Date:  1959-01

8.  Biliary transport and hepatic storage of sulfobromophthalein sodium in the unanesthetized dog, in normal man, and in patients with hepatic disease.

Authors:  H O WHEELER; J I MELTZER; S E BRADLEY
Journal:  J Clin Invest       Date:  1960-07       Impact factor: 14.808

  8 in total
  43 in total

1.  The effect of sodium salicylate on bile secretion in the dog.

Authors:  S C Rutishauser; S L Stone
Journal:  J Physiol       Date:  1975-03       Impact factor: 5.182

2.  Aspects of bile secretion in the rabbit.

Authors:  S C Rutishauser; S L Stone
Journal:  J Physiol       Date:  1975-03       Impact factor: 5.182

3.  Partial purification of two lithocholic acid-binding proteins from rat liver 100 000g supernatants.

Authors:  R C Strange; R Cramb; J D Hayes; I W Percy-Robb
Journal:  Biochem J       Date:  1977-09-01       Impact factor: 3.857

4.  Biliary electrolytes and enzymes in patients with and without gallstones.

Authors:  K J Ho
Journal:  Dig Dis Sci       Date:  1996-12       Impact factor: 3.199

5.  Bile salt secretion.

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

6.  Effects of taurodihydrofusidate, a bile salt analogue, on bile formation and biliary lipid secretion in the rhesus monkey.

Authors:  M Beaudoin; M C Carey; D M Small
Journal:  J Clin Invest       Date:  1975-12       Impact factor: 14.808

7.  The secretory characteristics of dehydrocholate in the dog: comparison with the natural bile salts.

Authors:  E R O'Máille; T G Richards
Journal:  J Physiol       Date:  1976-10       Impact factor: 5.182

8.  Choleresis and hepatic transport mechanisms. IV. Influence of bile salt choleresis on the hepatic transport of the organic cations, D-tubocurarine and N4 -acetyl procainamide ethobromide.

Authors:  R J Vonk; E Scholtens; G T Keulemans; D K Meijer
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1978-03       Impact factor: 3.000

9.  Liver structure and function following small bowel resection.

Authors:  M C Gupta; G Neale; R H Dowling
Journal:  Gut       Date:  1973-06       Impact factor: 23.059

10.  Alteration of bile canalicular enzymes in cholestasis. A possible cause of bile secretory failure.

Authors:  F R Simon; I M Arias
Journal:  J Clin Invest       Date:  1973-04       Impact factor: 14.808

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