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Untersuchungen an Glycerinphospholipiden aus weißer Substanz von MS- und Normalgehirnen

The glycerophospholipid content of the white matter of normal and MS brains

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Summary

In order to determine the total lipid content, as well as the fatty acid and aldehyde content of the two principal glycerophospholipid fractions, the cholinephosphatides and the ethanolaminephosphatides, 17 samples of normal looking white matter from various regions of four brains of MS patients, and 21 samples from the corresponding regions of five normal brains, were analyzed. The MS patients had suffered from the disease for 8 to 20 years and the diagnosis had been established histologically.

A statistically significant difference, expressed in mg/g of dry tissue weight, was found in the normal looking white matter of the MS brains compared with that of the normal brains, as follows:

  1. (1)

    The lipids in general and every lipidfraction itself (total cholesterol, phospholipids and glycolipids) were reduced.

  2. (2)

    The reduction of the different phospholipid families varied. The decrease of ethanolamineplasmalogens and of phosphatidylserines was the greatest (25%), whereas the remaining ethanolamine phospholipids and the phosphatidylcholines were nearly the same as in normal tissue.

  3. (3)

    Fatty acids of phosphatidylcholines showed a decrease of C18:0 and C18:1. The absolute amount of palmitic acid was by no means reduced, but seemed to be increased.

  4. (4)

    The fatty acids, a well as the aldehydes of the ethanolamine phospholipids, showed a decrease of C18:1. The other aldehydes were also diminished, as was also true for the C20:1 fatty acid.

We think it important that there was a difference in the amount of reduction in the phospholipid families and a decrease of the monounsaturated compounds in the main glycerophospholipids.

Zusammenfassung

Aus 4 MS-Gehirnen entnahmen wir 17 Proben von makroskopisch unveränderter weißer Substanz und verglichen sie hinsichtlich der Gesamtlipide, der Phospholipidzusammensetzung sowie der Fettsäuren und Aldehyde aus den cholin- bzw. ethanolaminhaltigen Phospholipiden mit 21 entsprechenden Proben aus 5 Normalgehirnen. Die weiße Substanz stammte vor allem aus den großen Marklagern des Frontal-, Parietal-, Occipital-Hirns und einiger anderer Regionen. Die Krankheitsdauer der Patienten betrug 8–20 Jahre. Die Diagnose war durch histologische Kontrollen gesichert.

Folgende Ergebnisse, gewonnen durch die Untersuchung der „normal“ erscheinenden weißen Substanz der MS-Gehirne, waren hoch signifikant — (angegeben in mg/g getr. Gewebe).

  1. 1.

    Die Gesamtlipide und die einzelnen Lipidfraktionen (Gesamtcholesterin, Phospholipide und Glycolipide) waren vermindert.

  2. 2.

    Die Abnahme der verschiedenen Phospholipidklassen war sehr unterschiedlich. Dabei zeigten die Ethanolaminplasmalogene und die serinhaltigen Phospholipide die stärkste Reduktion (etwa um 25%), während die übrigen Ethanolaminphospholipide im Material aus pathologischen Gehirnen in gleicher Menge wie in den normalen Proben vorlag. Das Phosphatidylcholin wies nur eine Abnahme von 5% auf.

  3. 3.

    Die Fettsäuren des Phosphatidylcholins zeigten eine Abnahme der C18:0-und C18:1-Verbindungen. Die absolute Menge der C16:0-Fettsäure war keineswegs vermindert. Sie war — allerdings nicht signifikant — angestiegen.

  4. 4.

    Sowohl bei den Fettsäuren als auch den Aldehyden der ethanolaminhaltigen Phospholipide hatten die C18:1-Verbindungen stark abgenommen. Bei den Aldehyden waren auch die anderen Komponenten betroffen, bei den Fettsäuren besonders auch die C20-Monoene.

Die spezifische Verminderung einiger Glycerinphospholipide wie auch die mehrfach anzutreffende Abnahme der Monoenverbindungen erscheint uns besonders bedeutsam.

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Abbreviations

PC:

Phosphatidylcholin (=Lecithin)

PE:

Phosphatidylethanolamine

FS:

Fettsäuren

FSME:

Fettsäuremethylester

DMA:

Dimethylacetale

Literatur

  1. Alling, Ch., Vanier, M. Th., Svennerholm, L.: Lipid alterations in apparently normal white matter in multiple sclerosis. Brain Research 35, 325–336 (1971)

    Google Scholar 

  2. Arnetoli, G., Pazzagli, A., Amaducci, L.: Fatty acid and aldehyde changes in choline- and ethanolamine-containing phospholipids in the white matter of multiple sclerosis brains. J. Neurochem. 16, 461–463 (1969)

    Google Scholar 

  3. Baker, R. W. R., Thompson, R. H. S., Zilkha, K. J.: Fatty-acid composition of brain lecithins in multiple sclerosis. Lancet 1963 I, 26–27

    Google Scholar 

  4. Baker, R. W. R., Thompson, R. H. S., Zilkha, K. J.: Changes in the amounts of linoleic acid in the serum of patients with multiple sclerosis. J. Neurol. Neurosurg. Psychiat. 29, 95–98 (1966)

    Google Scholar 

  5. Bartlett, G. R.: Phosphorus assay in column chromatography. J. Biol. Chem. 234, 466–468 (1959)

    Google Scholar 

  6. Clausen, J., Hansen, J. B.: Myelin constituents of human central nervous system. Acta Neurolog. Scandinav. 46, 1–17 (1970)

    Google Scholar 

  7. Cumings, J. N.: The cerebral lipids in disseminated sclerosis and in amaurotic family idiocy. Brain 76, 551–562 (1953)

    Google Scholar 

  8. Cumings, J. N.: Lipid chemistry of the brain in demyelinating diseases. Brain 78, 554–563 (1955)

    Google Scholar 

  9. Cumings, J. N., Goodwin, H.: Sphingolipids and phospholipids of myelin in multiple sclerosis. Lancet 1968 II, 664–665

    Google Scholar 

  10. Cumings, J. N., Shortman, R. C., Skrbic, T.: Lipid studies in the blood and brain in multiple sclerosis and motor neurone disease. J. clin. Path. 18, 641–644 (1965)

    Google Scholar 

  11. Davison, A. N., Wajda, M.: Cerebral lipids in multiple sclerosis. J. Neurochem. 9, 427–432 (1962)

    Google Scholar 

  12. Debuch, H., Mertens, W., Winterfeld, M.: Quantitative Bestimmung der Phosphatide mit Hilfe einer zweidimensionalen dünnschichtchromatographischen Methode. Hoppe-Seyler's Z. physiol. Chem. 349, 896–902 (1968)

    Google Scholar 

  13. Delmotte, P., Ketelaer, Ch. J.: Biochemical findings in multiple sclerosis. J. Neurol. 207, 27–43 (1974)

    Google Scholar 

  14. Dittmer, J. C., Lester, R. L.: A simple, specific spray for the detection of phospholipids on thin-layer chromatograms. J. Lipid Res. 5, 126–127 (1964)

    Google Scholar 

  15. Feulgen, R., Boguth, W., Andresen, G.: Quantitative Bestimmung der Acetalphosphatide (Plasmalogen) im Serum unter Berücksichtigung des „Waelsch-Effektes“. Hoppe-Seyler's Z. physiol. Chem. 287, 90–108 (1951)

    Google Scholar 

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

    Google Scholar 

  17. Gerstl, B., Kahnke, M. J., Smith, J. K., Tavaststjerna, M. G., Hayman, R. B.: Brain lipids in multiple sclerosis and other diseases. Brain 84, 310–319 (1961)

    Google Scholar 

  18. Gerstl, B., Tavaststjerna, M. G., Hayman, R. B., Eng, L. F., Smith, J. K.: Alterations in myelin fatty acids and plasmalogens in multiple sclerosis. Ann. N. Y. Acad. Sci. 122, 405–416 (1965)

    Google Scholar 

  19. Gerstl, B., Eng, L. F., Tavaststjerna, M. G., Smith, J. K., Kruse, S. L.: Lipids and proteins in multiple sclerosis white matter. J. Neurochem. 17, 677–689 (1970)

    Google Scholar 

  20. Kishimoto, Y., Radin, N. S., Tourtellotte, W. W., Parker, J. A., Itabashi, H. H.: Gangliosides and glycerophospholipids in multiple sclerosis white matter. Arch. Neurol. 16, 44–54 (1967)

    Google Scholar 

  21. Klenk, E., Debuch, H.: In: R. T. Holman, W. O. Lundberg, T. Malkin, eds., Progress in the chemistry of fats and other lipids, pp. 3–26. London: Pergamon Press 1963

    Google Scholar 

  22. Lea, C. H., Rhodes, D. N., Stoll, D. R.: Phospholipids. Biochem. J. 60, 353–363 (1955)

    Google Scholar 

  23. Rouser, G., Marinetti, G. V., Witter, R. F., Berry, J. F., Stotz, E.: Paper chromatography of phospholipids. J. Biol. Chem. 223, 485–497 (1956)

    Google Scholar 

  24. Suzuki, K., Kamoshita, S., Eto, Y., Tourtellotte, W. W., Gonatas, J. O.: Myelin in multiple Sclerosis. Arch. Neurol. 28, 293–297 (1973)

    Google Scholar 

  25. Svennerholm, L.: Distribution and fatty acid composition of phosphoglycerides in normal human brain. J. Lipid Res. 5, 570–579 (1968)

    Google Scholar 

  26. Thompson, R. H. S.: A biochemical approach to the problem of multiple sclerosis. Proc. roy. Soc. Med. 59, 269–276 (1966)

    Google Scholar 

  27. Winterfeld, M., Debuch, H.: Die Lipoide einiger Gewebe und Organe des Menschen. Hoppe-Seyler's Z. physiol. Chem. 345, 11–21 (1966)

    Google Scholar 

  28. Woelk, H., Borri, P.: Glycerinphosphatide und Sphingolipide der normalen weißen Substanz bei der Multiplen Sklerose. Z. Neurol. 205, 243–256 (1973)

    Google Scholar 

  29. Woelk, H., Borri, P.: Lipid and fatty acid composition of myelin purified from normal and MS brains. Europ. Neurol. 10, 250–260 (1973)

    Google Scholar 

  30. Yanagihara, T., Cumings, J. N.: Alterations of phospholipids, particularly plasmalogens in the demyelination of multiple sclerosis as compared with that of cerebral oedema. Brain 92, 59–70 (1969)

    Google Scholar 

  31. Zak, B., Dickenman, R. C., White, E. G., Burnett, H., Cherney, R. J.: Rapid estimation of free and total cholesterol. Amer. J. Clin. Path. 24, 1307–1315 (1954)

    Google Scholar 

  32. Zöllner, N., Wolfram, G.: Dünnschichtchromatographische Systeme zur Trennung der Plasmalipoide. Klin. Wschr. 40, 1101–1107 (1962)

    Google Scholar 

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Winterfeld, M., Debuch, H. Untersuchungen an Glycerinphospholipiden aus weißer Substanz von MS- und Normalgehirnen. J. Neurol. 215, 261–272 (1977). https://doi.org/10.1007/BF00312497

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