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Acylglycerol structure of genetic varieties of peanut oils of varying atherogenic potential

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Lipids

Abstract

Detailed investigation was made of the triacylglycerol structure of three varieties of peanut oils of varying atherogenic activity. By means of chromatographic and stereospecific analyses, it was shown that all the oils had markedly nonrandom enantiomeric structures with the long chain saturated fatty acids (C20−C24) confined exclusively to thesn-3-position, whereas the palmitic and oleic acids were distributed about equally between thesn-1-andsn-3-positions, with the linoleic acid being found preferentially in thesn-2-position. On the basis of detailed studies of the molecular species of the separatesn-1,2-,sn-2,3- andsn-1,3-diacylglycerol moieties, it was concluded that the fatty acids in the three positions of the glycerol molecule are combined with each other solely on the basis of their relative molar concentrations. As a result, it was possible to calculate the composition of the molecular species of the peanut oil triacylglycerols (including the content of the enantiomers and the reverse isomers) by means of the 1-random 2-random 3-random distribution. In general, the three peanut oils possessed triacylglycerol structures which where closely similar to that derived earlier for a commercial peanut oil of North American origin. Since their oil has exhibited a high degree of atherogenic potential, it was anticipated that the present oils would likewise be atherogenic, which has been confirmed by biological testing. However, there are certain differences in the triacylglycerol structures among these oils, which can be correlated with the variations in their atherogenic activity. The major differences reside in the linoleic/oleic acid ratios in the triacylglycerols, especially in thesn-2-position, and in the proportions in which these acids are combined with the long chain fatty acids. On the basis of the characteristic structures identified in the earlier analyzed atherogenic peanut oil, the peanut oil of South American origin would be judged to possess the greatest atherogenic potential and this has been borne out by biological testing.

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References

  1. Kritchevsky, D., Tepper, S.A., Vesselinovitch, D., and Wissler, R.W. (1973) Atherosclerosis 14, 53–64.

    Article  Google Scholar 

  2. Kritchevsky, D., Tepper, S.A., Vesselinovitch, D., and Wissler, R.W. (1973) Atherosclerosis 17, 225–243.

    Article  PubMed  CAS  Google Scholar 

  3. Myher, J.J., Marai, L., Kuksis, A., and Kritchevsky, D. (1977) Lipids 12, 775–785.

    Article  PubMed  CAS  Google Scholar 

  4. Kritchevsky, D., Tepper, S.A., Scott, D.A., Klurfeld, D.M., Vesselinovitch, D., and Wissler, R.W. (1981) Atherosclerosis 38, 291–299.

    Article  PubMed  CAS  Google Scholar 

  5. Myher, J.J., and Kuksis, A. (1979) Can. J. Biochem. 57, 117–124.

    Article  PubMed  CAS  Google Scholar 

  6. Kuksis, A., Breckenridge, W.C., Myher, J.J., and Kakis, G. (1978) Can. J. Biochem. 56, 630–639.

    PubMed  CAS  Google Scholar 

  7. Myher, J.J., Kuksis, A., Marai, L., and Yeung, S.K.F. (1978) Anal. Chem. 50, 557–561.

    Article  CAS  Google Scholar 

  8. Myher, J.J., Kuksis, A., Vasdev, S.C., and Kako, K.J. (1979) Can. J. Biochem. 57, 1315–1327.

    PubMed  CAS  Google Scholar 

  9. Kuksis, A., Marai, L., and Myher, J.J., (1973) J. Am. Oil Chem. Soc. 50, 193–201.

    PubMed  CAS  Google Scholar 

  10. Kuksis, A., and Marai, L. (1967) Lipids 2, 217–224.

    Article  CAS  PubMed  Google Scholar 

  11. Glass, R.L. (1971) Lipids 6, 919–925.

    Article  CAS  Google Scholar 

  12. Litchfield, C. (1972) Analysis of Triglycerides, pp. 248–261, Academic Press, New York.

    Google Scholar 

  13. Possmayer, F., Scherphof, G.L., Dubbelman T.N.A.R., and Van Deenen, L.L.M. (1969) Biochim. Biophys. Acta 176, 95–110.

    PubMed  CAS  Google Scholar 

  14. Huebscher, G. (1970) in Lipid Metabolism (Wakil, S.J., ed.) pp. 279–370, Academic Press, New York, NY.

    Google Scholar 

  15. Higgins, J.A., and Barnett, R.J. (1971) J. Cell Biol. 50, 102–120.

    Article  PubMed  CAS  Google Scholar 

  16. Ellingboe, J., and Steinberg, D. (1972) Biochim. Biophys. Acta 270, 92–102.

    PubMed  CAS  Google Scholar 

  17. Mattson, F.H., and Streck, J.A. (1974) J. Nutr. 104, 483–488.

    PubMed  CAS  Google Scholar 

  18. Mattson, F.H., Nolen, G.A., and Webb, M.R. (1979) J. Nutr. 109, 1682–1687.

    PubMed  CAS  Google Scholar 

  19. Sanders, T.H. (1979) Lipids 14, 630–633.

    Article  CAS  Google Scholar 

  20. Van Pee, W., Van Hee, J., Boni, L., and Hendrikx, A. (1979) J. Am. Oil Chem. Soc. 56, 901–903.

    Google Scholar 

  21. Hokes, J.C., and Worthington, R.E. (1979) J. Am. Oil Chem. Soc. 56, 953–956.

    CAS  Google Scholar 

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Manganaro, F., Myher, J.J., Kuksis, A. et al. Acylglycerol structure of genetic varieties of peanut oils of varying atherogenic potential. Lipids 16, 508–517 (1981). https://doi.org/10.1007/BF02535049

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  • DOI: https://doi.org/10.1007/BF02535049

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