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Lipid metabolism of brain tissue in culture

  • Published:
Lipids

Abstract

Tissue explants from frontal lobes of rat brain were used for the study of cerebral fatty acid metabolism. After tissues had been maintained in serum-supplemented medium, a lipid free medium was substituted and metabolic studies were carried out. Under these conditions explants continued to take up lipid precursors for at least 48 hr. Stearic acid 1-C14, palmitic acid 1-C14 and lignoceric acid 1-C14 were bound to cells as the free fatty acids or incorporafed into neutral lipids (particularly triglycerides), glycolipids and phospholipids. In the galactolipid fraction, cerebrosides were the principal radioactive lipids. Choline phosphoglycerides, ethanolamine phosphoglycerides, inositol phosphoglycerides and serine phosphoglycerides were the principal radioactive phospholipids. Fatty acids were incorporated into cellular lipids either unchanged or after desaturation, chain elongation, or both. In a patient with a demyelinating disease, precursor uptake was reduced and chain elongation and desaturation of the fatty acid was diminished. In a patient with generalized GM2 gangliosidosis, glycolipids other than cerebrosides were labeled to a greater extent than normal. These studies exemplify the usefulness of tissue explants for prolonged metabolic studies in normal and pathological specimens of brain.

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References

  1. Aeberhard, E., J. Grippo and J.H. Menkes, Pediat. Res. 3:590 (1969).

    PubMed  CAS  Google Scholar 

  2. Bailey, J.M. Biochim. Biophys. Acta 125:226 (1966).

    CAS  Google Scholar 

  3. Barbato, L., I. Wm. Barbato and A. Hamanaka, Brain Res. 7:399 (1968).

    Article  PubMed  CAS  Google Scholar 

  4. Fillerup, D.L., J.C. Migliore and J.F. Mead, J. Biol. Chem. 233:98 (1958).

    PubMed  CAS  Google Scholar 

  5. Gornall, A.G., C.J. Bardawill and M.M. David, J. Biol. Chem. 177:751 (1949).

    CAS  PubMed  Google Scholar 

  6. Jervis, G.A., Proc. Soc. Exp. Biol. Med. 81:715 (1952).

    PubMed  CAS  Google Scholar 

  7. Menkes, J.H. Neurochem. 18:1433 (1971).

    Article  CAS  Google Scholar 

  8. Menkes, J.H., et al., Arch. Neurol. 25:14 (1971).

    PubMed  CAS  Google Scholar 

  9. Morris, L.J. J. Lipid Res. 7:717 (1966).

    PubMed  CAS  Google Scholar 

  10. Morrison, W.R., and L.M. Smith, J. Lipid Res. 4:600 (1964).

    Google Scholar 

  11. O’Brien, J.S. Science 147:1099 (1965).

    Article  PubMed  CAS  Google Scholar 

  12. Perry, T.L., et al., New Eng. J. Med. 282:761 (1970).

    Article  PubMed  CAS  Google Scholar 

  13. Shah, S.N., N.A. Peterson and C.M. McKean, J. Neurochem. 17:279 (1970).

    Article  PubMed  CAS  Google Scholar 

  14. Skipski, V.P., R.F. Peterson and M. Barclay, Biochem. J. 90:374 (1964).

    PubMed  CAS  Google Scholar 

  15. Snyder, F., and N. Stephens, Analyt. Biochem. 4:128 (1962).

    Article  PubMed  CAS  Google Scholar 

  16. Sun, G.Y., and L.A. Horrocks, J. Neurochem. 16:181 (1969).

    Article  PubMed  CAS  Google Scholar 

  17. Weber, G., R.I. Glazer and R.A. Ross, Advances Enzym. Regulat. 8:13 (1970).

    Article  CAS  Google Scholar 

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Menkes, J.H. Lipid metabolism of brain tissue in culture. Lipids 7, 135–141 (1972). https://doi.org/10.1007/BF02532601

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  • DOI: https://doi.org/10.1007/BF02532601

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