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Comparison of the clearances of serum chylomicron triglycerides enriched with eicosapentaenoic acid or oleic acid

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Lipids

Abstract

Rat mesenteric lymph chylomicrons containing triglycerides enriched with either [14C]oleic acid (OA) or [14C]-eicosapentaenoic acid (EPA) were prepared by ultracentrifugation of lymph samples collected for 6 hr after a single duodenal infusion of an emulsion containing either fatty acid. These chylomicrons were injected into the jugular vein of recipient rats and, at various time intervals, blood was drawn and serum was assayed for radioactivity. In separate animals, serum lipoprotein fractions were separated by ultracentrifugation, and the redistribution of labeled fatty acid among circulating lipoproteins was determined by liquid scintillation spectrometry. When the early disappearance rates (10 min) of either total serum radioactivity or specifically the chylomicron fraction were compared, there were no differences between the groups receiving OA-or EPA-enriched chylomicrons. However, disappearance rates of EPA-enriched chylomicrons were slower than those of OA-enriched chylomicrons from 25 to 90 min. The small but significant differences in the disappearance rates for the longer time periods cannot be ascertained without further studies. At 5 min after injection of either type of chylomicron, the d<1.006 g/ml lipoprotein fraction of serum chylomicrons and very low density lipoproteins contained almost 90% of the original radioactivity. By 240 min, when less than 2% of the radioactivity remained, this radioactivity in the d<1.006 g/ml fraction was 43–46%, with concomitant increases in the low and high density lipoprotein fractions and in the lipoprotein-free serum.

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References

  1. Ahrens, E.H. (1959)Lancet 1, 115–119.

    Article  PubMed  Google Scholar 

  2. Bang, H.O., and Dyerburg, J. (1972)Acta Med. Scand. 192, 85–94.

    Article  PubMed  CAS  Google Scholar 

  3. Bronsgeest-Schonte, H.C., Van Geut, C.M., Luten, J.B., and Ruiter, A. (1981)Am. J. Clin. Nutr. 34, 1752–1757.

    Google Scholar 

  4. Goodnight, S.E. Jr., Harris, W.S., Connor, W.E., and Illingworth, E.E. (1982)Arteriosclerosis 2, 87–113.

    PubMed  CAS  Google Scholar 

  5. Peifer, J.J., Janssen, F., Ahn, P., Cox, W., and Lundberg, W.O. (1960)Arch. Biochem. Biophys. 86, 302–308.

    Article  PubMed  CAS  Google Scholar 

  6. Peifer, J.J., Lundberg, W.O., Shio, I., and Warmenar, E. (1965)Arch. Biochem. Biophys. 110 270–283.

    Article  PubMed  CAS  Google Scholar 

  7. Phillipson, B.E., Rothrock, D.W., Connor, W.E., Harris, W.S., and Illingworth, D.R. (1985)N. Engl. J. Med. 312, 1210–1219.

    Article  PubMed  CAS  Google Scholar 

  8. Iritani, N., Fukuda, E., Inoguchi, K., Tsubosaka, M., and Tashiro, S. (1980)J. Nutr. 110, 1664–1670.

    PubMed  CAS  Google Scholar 

  9. Iritani, N., and Norita, N. (1984)Biochim. Biophys. Acta 703, 441–447.

    Google Scholar 

  10. Wong, S.H., Nestel, P.J., Trimble, R.P., Stonere, G.B., Illman, R.J., and Topping, D.L. (1984)Biochim. Biophys. Acta 792, 103–109.

    PubMed  CAS  Google Scholar 

  11. Fischer, S., and Weber, P.C. (1984)Nature 307, 165–168.

    Article  PubMed  CAS  Google Scholar 

  12. Fischer, S., and Weber, P.C. (1983)Biochim. Biophys. Res. Commun. 116, 1091–1099.

    Article  CAS  Google Scholar 

  13. Needleman, P., Raz, A., Minkes, M.S., Ferrendelli, J.A., and Sprecher, H. (1979)Proc. Natl. Acad. Sci. USA 76, 944–948.

    Article  PubMed  CAS  Google Scholar 

  14. Bang, H.O., and Dyerberg, J. (1980) inAdvanced Nutrition Research (Draper, H.N., ed.) Vol. 3, pp. 1–22, Plenum Press, New York.

    Google Scholar 

  15. Hirai, A., Hamazaki, T., Terano, T., Nishikawa, T., Tamura, Y., Kumagai, A., and Sajiki, J. (1980)Lancet 2, 1132–1133.

    Article  PubMed  CAS  Google Scholar 

  16. Yotakis, L.D.O. (1981)Thromb. Haemost. 45, 65–68.

    Google Scholar 

  17. Harris, W.S., and Connor, W.E. (1980)Trans. Assoc. Am. Physicians 93, 148–155.

    PubMed  CAS  Google Scholar 

  18. Brockerhoff, H., Hoyle, R.J., and Huang, P.C. (1966)Can. J. Biochem. 44, 1519–1525.

    Article  CAS  Google Scholar 

  19. Bottino, N.R., Jandenberg, G.A., and Reiser, R. (1967)Lipids 2, 489–493.

    Article  CAS  PubMed  Google Scholar 

  20. Chen, I.S., Cassidy, M.M., Sherppard, A.J., and Vahouny, G.V.,Atherosclerosis, in press.

  21. Vahouny, G.V., Blendermann, E.M., Gallo, L.L., and Treadwell, C.R. (1980)J. Lipid Res. 21, 415–424.

    PubMed  CAS  Google Scholar 

  22. Chen, I.S., Satchithanandam, S., Cassidy, M.M., Sheppard, A.J., and Vahouny, G.V. (1985)J. Nutr. 115, 219–225.

    PubMed  CAS  Google Scholar 

  23. Havel, R.J., Eder, H.A., and Bragdon, J.H. (1955)J. Clin. Invest. 34, 1345–1353.

    PubMed  CAS  Google Scholar 

  24. Von Schacky, C., Fischer, S., and Weber, P. (1985)J. Clin. Invest. 76, 1626–1631.

    Article  Google Scholar 

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Chen, I.S., Le, T., Subramanian, S. et al. Comparison of the clearances of serum chylomicron triglycerides enriched with eicosapentaenoic acid or oleic acid. Lipids 22, 318–321 (1987). https://doi.org/10.1007/BF02533999

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  • DOI: https://doi.org/10.1007/BF02533999

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