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Turnover rate of molecular species of sphingomyelin in rat brain

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Abstract

Turnover rate of individual molecular species of sphingomyelin of adult rat brain myelin and microsomal membranes was determined after an intracerebral injection of 100 μCi of [C3H3]choline. Myelin and microsomal membrane sphingomyelins were isolated from the rest of the lipids. The individual molecular species of benzoylated sphingomyelin were separated and quantitated by reversed-phase high performance liquid chromatography. All individual major molecular species of microsomal and myelin sphingomyelin had maximum incorporation at 6 and 15 days, respectively, after the injection. The specific radioactivity of all the various molecular species of both myelin and microsomal sphingomyelin declined at a similar rate after reaching a maximum. There was no significant difference in the turnover rate of short chain (16:0, 18:0) and long chain (>22:0) fatty acid containing sphingomyelin. The average apparent turnover rate of myelin and microsomal sphingomyelin molecular species was about 14–16 days for the fast pool and about 45 days for the slow pool. It is concluded that individual molecular species of sphingomyelin of myelin and microsomal membranes turned over at a similar rate. Thus, turnover rate of sphingomyelin in myelin and microsomal membranes is not affected by the fatty acyl composition of the lipid.

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References

  1. Benjamins, J. A., andSmith, M. E. 1977. Metabolism of myelin. Pages 233–270. inP. Morell (ed.) Myelin. Plenum Press, New York.

    Google Scholar 

  2. Jungalwala, F. B., andDawson, R. M. C. 1971. The turnover of myelin phospholipids in the adult and developing rat brain. Biochem. J. 123:683–693.

    PubMed  Google Scholar 

  3. Jungalwala, F. B. 1974. The turnover of myelin phosphatidylcholine and sphingomyelin in adult rat brain. Brain Res. 78:99–108.

    PubMed  Google Scholar 

  4. Jungalwala, F. B. 1974. Synthesis and turnover of cerebroside sulfate of myelin in adult and developing rat brain. J. Lipid Res. 15:114–123.

    PubMed  Google Scholar 

  5. Hayes, L. W., andJungalwala, F. B. 1976. Synthesis and turnover of cerebroside and phosphatidylserine of myelin and microsomal fractions of adult and developing rat brain. Biochem. J. 160:195–204.

    PubMed  Google Scholar 

  6. Singh, H., andJungalwala, F. B. 1979. Turnover of myelin proteins in adult rat brain. Int. J. Neurosci. 9:123–131.

    PubMed  Google Scholar 

  7. Pasquini, J. M., Krawiec, L., andSoto, E. F. 1973. Turnover of phosphatidylcholine in cell membranes of adult rat brain. J. Neurochem. 21:647–653.

    PubMed  Google Scholar 

  8. Davison, A. N., andGregson, N. A. 1966. Metabolism of cellular membrane sulpholipids in rat brain. Biochem. J. 98:915–922.

    PubMed  Google Scholar 

  9. Horrocks, L. A., Toews, A. D., Thompson, D. K., andChin, J. Y. 1976. Synthesis and turnover of brain phosphoglycerides-results, methods of calculation and interpretation. Adv. Exptl. Med. Biol. 72:37–54.

    Google Scholar 

  10. Miller, S. L., Benjamins, J. A., andMorell, P. 1977. Metabolism of glycerophopholipids of myelin and microsomes in rat brain. Reutilization of precursors. J. Biol. Chem. 252:4026–4037.

    Google Scholar 

  11. Chapman, D. 1975. Phase transitions and fluidity characteristics of lipids and cell membranes. Quart. Rev. Biophys. 8:185–235.

    Google Scholar 

  12. Jungalwala, F. B., Hayssen, V., Pasquini, M., andMcCluer, R. H. 1979. Separation of molecular species of sphingomyelin by reversed-phase high performance liquid chromatography. J. Lipid Res. 20:579–587.

    PubMed  Google Scholar 

  13. Smith, M., Monchamp, P., andJungalwala, F. B. 1981. Separation of molecular species of complex-lipids by argentation and reversed-phase HPLC. J. Lipid Res. 22:714–719.

    PubMed  Google Scholar 

  14. Ruenwongsa, P., Singh, H., andJungalwala, F. B. 1979. Protein catalyzed exchange of phosphatidylinositol between rat brain microsomes and myelin. J. Biol. Chem. 254:9385–9393.

    PubMed  Google Scholar 

  15. Folch, P. J., Lees, M., andSloane-Stanley, G. H. 1957. A simple method for the isolation and purification of total lipids from animal tissues. J. Biol. Chem. 226:497–509.

    PubMed  Google Scholar 

  16. Jungalwala, F. B., Evans, J. E., andMcCluer, R. H. 1976. High-performance liquid chromatography of phosphatidylcholine and sphingomyelin with detection in the region of 200 nm. Biochem. J. 155:55–60.

    PubMed  Google Scholar 

  17. Dawson, R. M. C. 1967. Analysis of phosphatides and glycerolipids by chromatography of their partial hydrolysis or alcoholysis products. Pages 163–189.In G. V. Marinetti (ed.) Lipid Chromatographic Analysis Vol. 1, M. Dekker, New York.

    Google Scholar 

  18. Freysz, L., andMandel, P. 1980. Turnover of molecular species of sphingomyelin in microsomes and myelin of rat brain. J. Neurochem. 34:305–308.

    PubMed  Google Scholar 

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LeBaron, F.N., Sanyal, S. & Jungalwala, F.B. Turnover rate of molecular species of sphingomyelin in rat brain. Neurochem Res 6, 1081–1089 (1981). https://doi.org/10.1007/BF00964414

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  • DOI: https://doi.org/10.1007/BF00964414

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