Skip to main content
The Journal of Clinical Investigation logoLink to The Journal of Clinical Investigation
. 1972 Jun;51(6):1337–1350. doi: 10.1172/JCI106930

Biliary excretion of lecithin and cholesterol in the dog

Henry O Wheeler 1, Katherine K King 1
PMCID: PMC292271  PMID: 5024035

Abstract

The biliary excretion rates of bile acid, lecithin, and cholesterol were measured in unanesthetized dogs after interruption of enterohepatic circulation and during infusions of sodium taurocholate, sodium glycocholate, sodium dehydrocholate, SC2644 (a bicyclic organic acid with high choleretic potency), and secretin. Both lecithin output and cholesterol output were directly related to bile acid excretion rate. The curves describing these relationships were concave downward. Molar concentration ratios of lecithin-to-bile acid declined gradually from approximately 0.4 to 0.2 as bile acid output increased from approximately 1 to 70 μmoles/min. Cholesterol-to-lecithin molar ratios were highest (0.05-0.15) at very low rates of bile acid excretion, but descended rapidly to a plateau (0.03-0.04) which was constant over the entire range of bile acid excretion rates from 10 to 70 μmoles/min.

Similar lipid excretion patterns were observed during glycocholate infusion, but secretin-induced choleresis and dehydrocholate-induced choleresis were unaccompanied by any increments in lecithin or cholesterol excretion and SC2644 (which caused a marked increase in canalicular bile production as measured by erythritol clearance) caused a depression of lipid excretion.

The data are consistent with the view that lecithin moves passively from cell membranes to intracanalicular micelles, that transport of cholesterol is coupled to lecithin transport, and that there is also a small amount of independent passive transport of cholesterol from membranes to micelles. A model developed on these assumptions has been shown to behave in a fashion consistent with the entire range of these observations.

Full text

PDF
1337

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. ABEL L. L., LEVY B. B., BRODIE B. B., KENDALL F. E. A simplified method for the estimation of total cholesterol in serum and demonstration of its specificity. J Biol Chem. 1952 Mar;195(1):357–366. [PubMed] [Google Scholar]
  2. Admirand W. H., Small D. M. The physicochemical basis of cholesterol gallstone formation in man. J Clin Invest. 1968 May;47(5):1043–1052. doi: 10.1172/JCI105794. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. BARTLETT G. R. Phosphorus assay in column chromatography. J Biol Chem. 1959 Mar;234(3):466–468. [PubMed] [Google Scholar]
  4. Balint J. A., Beeler D. A., Kyriakides E. C., Treble D. H. The effect of bile salts upon lecithin synthesis. J Lab Clin Med. 1971 Jan;77(1):122–133. [PubMed] [Google Scholar]
  5. Bourgès M., Small D. M., Dervichian D. G. Biophysics of lipid associations. 3. The quaternary systems lecithin-bile salt-cholesterol-water. Biochim Biophys Acta. 1967 Oct 2;144(2):189–201. [PubMed] [Google Scholar]
  6. Boyer J. L., Klatskin G. Canalicular bile flow and bile secretory pressure. Evidence for a non-bile salt dependent fraction in the isolated perfused rat liver. Gastroenterology. 1970 Dec;59(6):853–859. [PubMed] [Google Scholar]
  7. Entemnan C., Holloway R. J., Albright M. L., Leong G. F. Bile acids and lipid metabolism. I. Stimulation of bile lipid excretion by various bile acids. Proc Soc Exp Biol Med. 1968 Apr;127(4):1003–1006. doi: 10.3181/00379727-127-32855. [DOI] [PubMed] [Google Scholar]
  8. Erlinger S., Dhumeaux D., Berthelot P., Dumont M. Effect of inhibitors of sodium transport on bile formation in the rabbit. Am J Physiol. 1970 Aug;219(2):416–422. doi: 10.1152/ajplegacy.1970.219.2.416. [DOI] [PubMed] [Google Scholar]
  9. Forker E. L. The effect of estrogen on bile formation in the rat. J Clin Invest. 1969 Apr;48(4):654–663. doi: 10.1172/JCI106023. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Forker E. L. Two sites of bile formation as determined by mannitol and erythritol clearance in the guinea pig. J Clin Invest. 1967 Jul;46(7):1189–1195. doi: 10.1172/JCI105612. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. GUNTER M. J., KIM K. S., MAGEE D. F., RALSTON H., IVY A. C. The choleretic potencies of some synthetic compounds. J Pharmacol Exp Ther. 1950 Aug;99(41):465–478. [PubMed] [Google Scholar]
  12. Heath T., Caple I. W., Redding P. M. Effect of the enterohepatic circulation of bile salts on the flow of bile and its content of bile salts and lipids in sheep. Q J Exp Physiol Cogn Med Sci. 1970 Apr;55(2):93–103. doi: 10.1113/expphysiol.1970.sp002067. [DOI] [PubMed] [Google Scholar]
  13. ISAKSSON B. On the dissolving power of lecithin and bile salts for cholesterol in human bladder bile. Acta Soc Med Ups. 1954 Sep 30;59(5-6):296–306. [PubMed] [Google Scholar]
  14. KAY R. E., ENTENMAN C. Stimulation of taurocholic acid synthesis and biliary excretion of lipids. Am J Physiol. 1961 Apr;200:855–859. doi: 10.1152/ajplegacy.1961.200.4.855. [DOI] [PubMed] [Google Scholar]
  15. Nilsson S., Scherstén T. Importance of bile acids for phospholipid secretion into human hepatic bile. Gastroenterology. 1969 Nov;57(5):525–532. [PubMed] [Google Scholar]
  16. Nilsson S., Scherstén T. Influence of bile acids on the synthesis of biliary phospholipids in man. Eur J Clin Invest. 1970 Aug;1(2):109–111. doi: 10.1111/j.1365-2362.1970.tb00606.x. [DOI] [PubMed] [Google Scholar]
  17. O'Máille E. R., Richards T. G., Short A. H. 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. J Physiol. 1966 Oct;186(2):424–438. doi: 10.1113/jphysiol.1966.sp008044. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. PREISIG R., COOPER H. L., WHEELER H. O. The relationship between taurocholate secretion rate and bile production in the unanesthetized dog during cholinergic blockade and during secretin administration. J Clin Invest. 1962 May;41:1152–1162. doi: 10.1172/JCI104568. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Small D. M. The formation of gallstones. Adv Intern Med. 1970;16:243–264. [PubMed] [Google Scholar]
  20. Swell L., Bell C. C., Jr, Entenman C. Bile acids and lipid metabolism. 3. Influence of bile acids on phospholipids in liver and bile of the isolated perfused dog liver. Biochim Biophys Acta. 1968 Oct 22;164(2):278–284. [PubMed] [Google Scholar]
  21. Swell L., Entenman C., Leong G. F., Holloway R. J. Bile acids and lipid metabolism. IV. Influence of bile acids on biliary and liver organelle phospholipids and cholesterol. Am J Physiol. 1968 Dec;215(6):1390–1396. doi: 10.1152/ajplegacy.1968.215.6.1390. [DOI] [PubMed] [Google Scholar]
  22. TALALAY P. Enzymic analysis of steroid hormones. Methods Biochem Anal. 1960;8:119–143. doi: 10.1002/9780470110249.ch3. [DOI] [PubMed] [Google Scholar]
  23. Tamesue N., Juniper K., Jr Concentrations of bile salts at the critical micellar concentration of human gall bladder bile. Gastroenterology. 1967 Mar;52(3):473–479. [PubMed] [Google Scholar]
  24. Wheeler H. O., Mancusi-Ungaro P. L. Role of bile ducts during secretin choleresis in dogs. Am J Physiol. 1966 May;210(5):1153–1159. doi: 10.1152/ajplegacy.1966.210.5.1153. [DOI] [PubMed] [Google Scholar]
  25. Wheeler H. O., Ramos O. L. DETERMINANTS OF THE FLOW AND COMPOSITION OF BILE IN THE UNANESTHETIZED DOG DURING CONSTANT INFUSIONS OF SODIUM TAUROCHOLATE. J Clin Invest. 1960 Jan;39(1):161–170. doi: 10.1172/JCI104015. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Wheeler H. O., Ross E. D., Bradley S. E. Canalicular bile production in dogs. Am J Physiol. 1968 Apr;214(4):866–874. doi: 10.1152/ajplegacy.1968.214.4.866. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Clinical Investigation are provided here courtesy of American Society for Clinical Investigation

RESOURCES