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Research Article| Volume 73, ISSUE 1, P34-41, January 1969

Effect of secretin on bile osmolality

  • William G.M. Hardison
    Footnotes
    Affiliations
    From the Thorndike Memorial Laboratory, II and IV (Harvard) Medical Services, Sears Surgical Laboratory, V (Harvard) Surgical Service, Boston City Hospital, Departments of Medicine and Surgery, Harvard Medical School Boston, Mass., USA
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  • J.C. Norman
    Affiliations
    From the Thorndike Memorial Laboratory, II and IV (Harvard) Medical Services, Sears Surgical Laboratory, V (Harvard) Surgical Service, Boston City Hospital, Departments of Medicine and Surgery, Harvard Medical School Boston, Mass., USA
    Search for articles by this author
  • Author Footnotes
    ∗ Present address: Section of Gastroenterology, Presbyterian-St. Luke's Hospital, 1753 West Congress Parkway, Chicago, Ill. 60612.
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      Abstract

      During a series of investigations upon the physiologic action of secretin on bile composition and flow from the perfused pig liver, we noted that in 7 of 8 experiments, bile osmolality increased with secretin stimulation. This increase implied that the secretin-stimulated fraction of bile was hypertonic to the basal or control fraction of bile. However, the nonideal osmotic behavior of bile salts upon dilution with electrolyte solution could explain the higher osmolality of secretin-stimulated bile. Bile salts above a certain critical micellar concentration (CMC) aggregate to form micelles which are in equilibrium with the monomer at the CMC. Dilution even with a solution that is isosmotic by virtue of another solute causes dissociation of micelles so that the concentration of the monomer is maintained constant at a concentration equal to the CMC. This results in more osmotically active particles than predicted from simple linear dilution of an ideal solution. We tested this theory by mixing solutions of bile salt (sodium cholate or taurocholate) and of pig bile with pure electrolyte solutions of approximately equal osmolality. The resultant osmolality was always greater than that predicted from ideal behavior. We mixed control bile samples from a perfused pig liver with an artificial electrolyte solution made to approximate the calculated secretin fraction from the same liver. The increase in osmolality with mixing was similar to that observed in bile collected from the liver during secretin stimulation. We conclude that the nonideal osmotic behavior of bile salt solutions can account for the increase in bile osmolality observed in our preparation during secretin stimulation. Future studies involving bile osmolality must take into account this behavior of bile salts.
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      References

        • Hardison W.G.
        • Norman J.C.
        Electrolyte composition of the secretin fraction of bile from the perfused pig liver.
        Am. J. Physiol. 1968; 214: 758
        • 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; 41: 1152
        • Norman J.C.
        • Franco F.O.
        • Brown M.E.
        • Seravis C.A.
        • Ackroyd F.W.
        • McDermott W.V.
        Techniques of obtaining and preparing the porcine liver for experimental and clinical temporary ex-vivo perfusion.
        J. S. Res. 1966; 6: 117
        • Hofmann A.F.
        Thin-layer absorption chromatography of free and conjugated bile acids on silicic acid.
        J. Lipid Res. 1962; 3: 127
        • Moore E.W.
        • Dietschy J.M.
        Na and K activity coefficients in bile and bile salts determined by glass electrodes.
        Am. J. Physiol. 1964; 206: 1111
        • Hofmann A.F.
        • Small D.M.
        Detergent properties of bile salts: Correlation with physiological function.
        Ann. Rev. Med. 1967; 18: 333
        • Hofmann A.F.
        The function of bile salts in fat absorption.
        Biochem. J. 1963; 89: 57
        • Wheeler H.O.
        • Mancusi-Ungaro P.L.
        Role of bile ducts during secretin choleresis in dogs.
        Am. J. Physiol. 1966; 210: 1153
        • Roepke R.R.
        • Mason H.L.
        Micelle formation in aqueous solutions of bile salts.
        J. Biol. Chem. 1940; 133: 103