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Measurement of bile acid synthesis in man by release of14CO2 from [26-14C]cholesterol: Comparison to isotope dilution and assessment of optimum reference cholesterol specific activity

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Lipids

Abstract

Bile acid synthesis can be measured as release of14CO2 from [26-14C]cholesterol divided by cholesterol specific activity, but this method has not been validated in human subjects. We made twelve comparisons of this CO2 method to standard isotope dilution in six normal subjects and found a mean discrepancy of 6%. Linear regression analysis of one value with respect to the other revealed a correlation coefficient of 0.83 (P<0.001), a Y-intercept close to zero (−4.98) and a slope close to 1 (1.06), suggesting good correspondence between the two methods. To assess the potential for error arising from use of serum cholesterol to estimate specific activity of cholesterol used for bile acid synthesis, we compared synthesis measured using serum free cholesterol specific activity to that measured using bile cholesterol specific activity, which is known to be near isotopic equilibrium with the precursor pool used for bile acid synthesis. Synthesis calculated in these two ways differed by less than 10%. The data indicate that the CO2 method using either serum or bile cholesterol specific activity provides a valid estimate of bile acid synthesis in man.

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References

  1. Lindstedt, S. (1957)Acta Phys. Scand. 40, 1–40.

    Article  Google Scholar 

  2. Grundy, S.M., Ahrends, Jr., E.H., and Miettinen, T.A. (1965)J. Lipid Res. 6, 397–410.

    PubMed  CAS  Google Scholar 

  3. Myant, N.B., and Lewis, B. (1966)Clin. Sci. 30, 117–127.

    PubMed  CAS  Google Scholar 

  4. Redinger, R.N., Chow, L., and Grace, D.M. (1978)Amer. J. Physiol. 235, R55-R63.

    PubMed  CAS  Google Scholar 

  5. Duane, W.C., Levitt, D.G., and Mueller, S.M. (1983)J. Clin. Invest. 72, 1930–1936.

    PubMed  CAS  Google Scholar 

  6. Schwartz, C.C., Berman, M., Vlahcevic, Z.R., Halloran, L.G., Gregory, D.H., and Swell, L. (1978)J. Clin. Invest. 61, 408–423.

    Article  PubMed  CAS  Google Scholar 

  7. Mitchell, J.C., Logan, G.M., Stone, B.G., and Duane, W.C. (1991)J. Lipid Res. 32, 71–78.

    PubMed  CAS  Google Scholar 

  8. Mitchell, J.C., Stone, B.G., Logan, G.M., and Duane, W.C. (1991)J. Lipid Res. 32, 1143–1149.

    PubMed  CAS  Google Scholar 

  9. Duane, W.C. (1978)J. Lab. Clin. Med. 91, 969–978.

    PubMed  CAS  Google Scholar 

  10. Grundy, S.M., and Metzger, A.L. (1972)Gastroenterology 62, 1200–1217.

    PubMed  CAS  Google Scholar 

  11. Duane, W.C., Holloway, D.E., Hutton, S.W., Corcoran, P.J., and Haas, N.A. (1982)Lipids 17, 345–348.

    PubMed  CAS  Google Scholar 

  12. Davidson, N.O., Samuel, P., Lieberman, S., Shane, S.P., Crouse, J.R., and Ahrens, Jr., E.H. (1981)J. Lipid Res. 22, 620–631.

    PubMed  CAS  Google Scholar 

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Mitchell, J.C., Stone, B.G. & Duane, W.C. Measurement of bile acid synthesis in man by release of14CO2 from [26-14C]cholesterol: Comparison to isotope dilution and assessment of optimum reference cholesterol specific activity. Lipids 27, 68–71 (1992). https://doi.org/10.1007/BF02537063

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  • DOI: https://doi.org/10.1007/BF02537063

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