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Atherosclerosis and plasma and liver lipids in nine inbred strains of mice

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Lipids

Abstract

Nine inbred strains of mice, which are progenitors of recombinant inbred sets, were evaluated for aortic lesion formation and plasma and liver lipid levels. This survey was done to determine if a semi-synthetic high-fat diet could elicit the same extent of diet-induced atherosclerosis as that observed in mice fed a natural ingredient highfat diet and to discover strain-specific plasma and liver lipid variants for future genetic characterization. Evaluation of aortic lesions after 18 wk of diet consumption showed that strains C57BL/6J, C57L/J, SWR/J and SM/J were susceptible to atherosclerosis and that A/J, AKR/J, C3H/HeJ, DBA/2J and SJL/J were relatively resistant. High-density lipoprotein cholesterol (HDL-C) levels were negatively correlated to lesion formation. Susceptible strains had decreased HDL-C levels when switched from chow to the semi-synthetic high-fat, high cholesterol diet, whereas resistant strains either showed no change or a slight increase in HDL-C levels. The exception to this pattern was found in SM mice, which were susceptible to aortic lesion formation but maintained the same HDL-C level on both chow and high-fat diets. HDL size differed among the strains, and levels of plasma apolipoprotein A-I and A-II correlated with HDL-C levels. Liver damage was not correlated to HDL-C levels or to susceptibility to atherosclerosis. Mice from strain A, which are resistant to atherosclerosis, had evidence of liver damage as observed by elevated levels of plasma alanine aminotransferase activity, by liver histology, by increased liver weight and by exceptionally high hepatic cholesterol content. For all strains, the levels of liver cholesterol and triglycerides were inversely correlated with each other; phospholipids did not vary greatly among strains. No remarkable differences in hepatic fatty acid profile were noted among the strains fed the atherogenic diet, but the fatty acid profile did differ considerably from that found in the diet itself.

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Abbreviations

ALT:

alanine aminotransferase

apo A-I:

apolipoprotein A-I

apo-II:

apolipoprotein A-II

BW:

body weight

EDTA:

ethylenediaminetetraacetic acid

HDL-C:

high-density lipoprotein cholesterol

LDL-C:

low-density lipoprotein cholesterol

TC:

total cholesterol

VLDL:

very low density lipoprotein

References

  1. Lyons, M.F., and Searle, A.G. (eds.) (1989)Genetic Variants and Strains of the Laboratory Mouse, 2nd edn., pp. 632–648, Oxford University Press, New York.

    Google Scholar 

  2. Paigen, B., Morrow, A., Holmes, P.A., Mitchell, D., and Williams, R.A. (1987)Atherosclerosis 68, 231–240.

    Article  PubMed  CAS  Google Scholar 

  3. Roberts, A., and Thompson, J. (1977)Progr. Biochem. Pharmacol. 13, 298–308.

    CAS  Google Scholar 

  4. Paigen, B., Morrow, A., Brandon, C., Mitchell, D., and Holmes, P. (1985)Atherosclerosis 57, 65–73.

    Article  PubMed  CAS  Google Scholar 

  5. Paigen, B., Ishida, B.Y., Verstuyft, J., Winters, R.B., and Albee, D. (1990)Arteriosclerosis 10, 316–323.

    PubMed  CAS  Google Scholar 

  6. Nishina, P.M., Verstuyft, J., and Paigen, B. (1990)J. Lipid Res. 31, 859–869.

    PubMed  CAS  Google Scholar 

  7. Izzo, C., Grillo, F., and Murado, E. (1981)Clin. Chem. 27, 371–374.

    PubMed  CAS  Google Scholar 

  8. Mancini, G., Carbonara, A.O., and Heremans, J.F. (1965)Immunochem. 2, 235–254.

    Article  CAS  Google Scholar 

  9. Lindgren, F.T. (1975) inAnalyses of Lipids and Lipoproteins (Perkins, E.G., ed.) pp. 204–224, American Oil Chemists’ Society, Champaign.

    Google Scholar 

  10. Blanche, P.G., Gong, G.L., Forte, T.M. and Nichols, A.U. (1981)Biochim. Biophys. Acta 665, 408–419.

    PubMed  CAS  Google Scholar 

  11. Folch, J., Lees, M., and Sloane-Stanley, G.H. (1957)J. Biol. Chem. 226, 497–509.

    PubMed  CAS  Google Scholar 

  12. Fletcher, M.J. (1968)Clin. Chim. Acta 22, 393–397.

    Article  PubMed  CAS  Google Scholar 

  13. Allain, C.C., Poon, L.S., Chang, C.S.G., Richmond, W., and Fu, P.C. (1974)Clin. Chem. 20, 470–475.

    PubMed  CAS  Google Scholar 

  14. Rouser, G. (1970)Lipids, 5, 494–496.

    Article  PubMed  CAS  Google Scholar 

  15. Aubert, R., Perdereau, D., Roubiscoul, M., Herzog, J., and Lemonnier, D. (1988)Lipids 23, 48–54.

    Article  PubMed  CAS  Google Scholar 

  16. Stewart-Phillips, J.L., Lough, J., and Skamene, E. (1989)Clin. Invest. Med. 12, 121–126.

    PubMed  CAS  Google Scholar 

  17. Paigen, B., Mitchell, D., Reue, K., Morrow, A., Lusis, A.J., and LeBoeuf, R.C. (1987)Proc. Natl. Acad. Sci. USA 84, 3763–3767.

    Article  PubMed  CAS  Google Scholar 

  18. Paigen, B., Nesbitt, M.N., Mitchell, D., Albee, D., and LeBoeuf, R.C. (1989)Genetics, 122, 163–168.

    PubMed  CAS  Google Scholar 

  19. Rubin, E.M., Krauss, R.M., Spangler, E.A., Verstuyft, J.G., and Clift, S.M. (1991)Nature 353, 265–269.

    Article  PubMed  CAS  Google Scholar 

  20. Hwa, J.J., Zollman, S., Warden, C.H., Taylor, B.A., Edwards, P.A., Fogelman, A.M., and Lusis, A.J. (1992)J. Lipid Res. 33, 711–725.

    PubMed  CAS  Google Scholar 

  21. Ishida, B.Y., Blanche, P.J., Nichols, A.V., and Yashar, M. (1991)J. Lipid Res. 32, 559–568.

    PubMed  CAS  Google Scholar 

  22. Jiao, S., Cole, T., Kitchens, T.T., Pfleger, B., and Schonfeld, G. (1990)Metabolism 39, 155–160.

    Article  PubMed  CAS  Google Scholar 

  23. Woollett, L.A., Spady, B.K., and Dietschy, J.M. (1989)J. Clin. Invest. 84, 119–128.

    Article  PubMed  CAS  Google Scholar 

  24. Srivastava, R.A.K., Jiao, S., Tang, J., Pfleger, B.A., Kitchens, R.T., and Schonfeild, G. (1991)Biochim. Biophys. Acta 1086, 29–43.

    PubMed  CAS  Google Scholar 

  25. Beynen, A.C., Katan, M.B., and Van Zutphen, L.F.M. (1987)Adv. Lipid Res., 22, 115–171.

    PubMed  CAS  Google Scholar 

  26. Lusis, A.J., Taylor, B.A., Quon, D., Zollman, S., and LeBoeuf, R.C. (1987)J. Biol. Chem. 262, 7594–7604.

    PubMed  CAS  Google Scholar 

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Nishina, P.M., Wang, J., Toyofuku, W. et al. Atherosclerosis and plasma and liver lipids in nine inbred strains of mice. Lipids 28, 599–605 (1993). https://doi.org/10.1007/BF02536053

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