Skip to main content
Log in

Influence of dietary fat on bile acid secretion of rats after portal injection of3H-cholesterol and [4-14C] cholesteryl esters

  • Published:
Lipids

Abstract

Labeled cholesterol and its esters were injected via the portal vein into bile duct-cannulated rats, subsequent to a 7 week regimen of either 5% safflower oil or 5% beef tallow in a hypercholesterolemic diet. Analysis of bile collected over a 6 hr period from the safflower group showed 8.6% higher output of bile acids, 13.6% higher conversion of3H-cholesterol to bile acids and 40% higher conversion of [4-14C]cholesteryl oleate to bile acids than bile collected from the tallow group. During the 1st hr conversion of both oleyl and linoleyl esters of14C-cholesterol to bile acids was much slower than conversion of the free3H-cholesterol to bile acids, thus eliminating these esters as preferred substrate for bile acid formation. However at 6 hr two-thirds of the injected14C of oleyl ester was recovered in the liver, and about half of this was in the form of free cholesterol. Thus cholesterol ester hydrolase, though inhibited by dietary cholesterol, evidently did not impose limitations on formation of free cholesterol for subsequent oxidation reactions. Specific radioactivities were of doubtful significance because of uncertainities as to “active” pool size. The data suggest that dietary linoleate exerts its hypocholesterolemic effect in some manner other than ester formation and that its point of action involves stimulation of cholesterol oxidation to bile acids.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. McGovern, R. F., and F. W. Quackenbush, Lipids 8:470 (1973).

    PubMed  CAS  Google Scholar 

  2. Byers, S. O., and M. Friedman, Proc. Soc. Exp. Biol. Med. 98:523 (1958).

    PubMed  CAS  Google Scholar 

  3. Wilson, J. D., and M. D. Siperstein, Amer. J. Physiol. 196:596 (1959).

    PubMed  CAS  Google Scholar 

  4. Kritchevsky, D., R. R. Kolman, M. W. Whitehouse, M. C. Cottrell and E. Staple, J. Lipid Res. 1:83 (1959).

    CAS  Google Scholar 

  5. Klevay, L. M., and D. M. Hegsted, J. Atheroscler. Res. 8:329 (1968).

    Article  PubMed  CAS  Google Scholar 

  6. Lewis, B., T. R. E. Pilkington and K. A. Hodd, Clin. Sci. 20:249 (1961).

    PubMed  CAS  Google Scholar 

  7. Thompson, G. R., R. K. Ockner and K. J. Isselbacher, J. Clin. Invest. 48:87 (1969).

    PubMed  CAS  Google Scholar 

  8. Norman, A., Arkivi Kemi 8:331 (1955).

    CAS  Google Scholar 

  9. Mattson, F. H., and R. A. Volpenhein, J. Lipid Res. 2:58 (1961).

    CAS  Google Scholar 

  10. Levin, S. J., J. L. Irvin and C. G. Johnston, Anal. Chem. 33:856 (1961).

    Article  CAS  Google Scholar 

  11. Deykin, D., and D. S. Goodman, J. Biol. Chem. 237:3649 (1962).

    PubMed  CAS  Google Scholar 

  12. Pinter, K. G., J. G. Hamilton and J. E. Muldrey, J. Lipid Res. 5:273 (1964).

    PubMed  CAS  Google Scholar 

  13. Myant, N. B., and H. A. Eder, Ibid. 2:363 (1961).

    CAS  Google Scholar 

  14. Shefer, S., S. Hauser, I. Bekersky and E. H. Mosbach Ibid. 10:646 (1969).

    PubMed  CAS  Google Scholar 

  15. Lowry, O. H., N. J. Rosebrough, A. L. Farr and R. J. Randall, J. Biol. Chem. 193:265 (1951).

    PubMed  CAS  Google Scholar 

  16. Ogura, M., J. Shiga and K. Yamasaki, J. Biochem. (Tokyo) 70:967 (1971).

    CAS  Google Scholar 

  17. Quarfordt, S. H., and D. S. Goodman, J. Lipid Res. 8:264 (1967).

    PubMed  CAS  Google Scholar 

  18. Boyd, G. S., Fed. Proc. 21:86 (1962).

    PubMed  CAS  Google Scholar 

  19. Swell, L., and M. D. Law, Arch. Biochem. Biophys. 112:115 (1965).

    Article  PubMed  CAS  Google Scholar 

  20. Swell, L., and M. D. Law, Ibid. 113:143 (1966).

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Journal Paper No. 4938 EAS, Purdue University.

About this article

Cite this article

McGovern, R.F., Quackenbush, F.W. Influence of dietary fat on bile acid secretion of rats after portal injection of3H-cholesterol and [4-14C] cholesteryl esters. Lipids 8, 473–478 (1973). https://doi.org/10.1007/BF02531767

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02531767

Keywords

Navigation