Literature DB >> 5640502

Changes in the fatty acid composition of cerebrosides and sulfatides of human nervous tissue with age.

L Svennerholm, S Ställberg-Stenhagen.   

Abstract

Sphingogalactolipids (galactocerebrosides and sulfatides) have been isolated in almost quantitative yields from normal human nervous tissue (mostly brain) at different ages and their fatty acid compositions have been determined by gas-liquid chromatography. The ratio of hydroxy acids to normal acids increased slightly during myelination and then remained rather constant; in adults the ratio for cerebrosides was about 2, and for sulfatides, 0.6-0.8. In adult nervous tissue the two predominant fatty acids of cerebrosides and sulfatides were the C(24) monounsaturated and 2-hydroxy saturated acids. The infant brain galactolipids had (compared with child and adult) a lower percentage of C(22)-C(26) fatty acids and a much lower percentage of monoenoic acids, both of normal and hydroxy acids. Low activities of fatty acid elongation and desaturation systems during myelination are inferred. Fatty acid changes with age were the same for cerebrosides and sulfatides but occurred later in the sulfatides, which supports the hypothesis that the cerebrosides are precursors of the sulfatides. The adult pattern of fatty acid composition with regard to degree of unsaturation and total percentage of C(22)-C(26) acids was reached as early as at 2 yr of age, but the percentage of odd-numbered (C(23) and C(25)) fatty acids continued to increase up to the age of 10-15 yr. The fatty acid composition of the galactolipids of peripheral nerves differed mainly in its lower percentages of C(25) and C(26) acids and higher percentages of C(22) and C(16) acids. This composition is thus intermediate between those of brain and of extraneural organs.

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Year:  1968        PMID: 5640502

Source DB:  PubMed          Journal:  J Lipid Res        ISSN: 0022-2275            Impact factor:   5.922


  31 in total

Review 1.  Brain development and assessing the supply of polyunsaturated fatty acid.

Authors:  M T Clandinin
Journal:  Lipids       Date:  1999-02       Impact factor: 1.880

2.  Harnessing the power of yeast to elucidate the role of sphingolipids in metabolic and signaling processes pertinent to psychiatric disorders.

Authors:  Shyamalagauri Jadhav; Miriam L Greenberg
Journal:  Clin Lipidol       Date:  2014-11-01

3.  The effect of undernutrition on the development of myelin in the rat central nervous system.

Authors:  M A Fishman; P Madyastha; A L Prensky
Journal:  Lipids       Date:  1971-07       Impact factor: 1.880

4.  The lipids of mitochondria of human gray and white matter.

Authors:  B Gerstl; L F Eng; R B Hayman; P Bond
Journal:  Lipids       Date:  1969-11       Impact factor: 1.880

5.  Experimental studies on the pathogenesis of leucodystrophies. 3. Cellular accumulation of injected sulphatides in brain, peripheral nerve and kidney.

Authors:  H A Hansson; Y Olsson; P Sourander
Journal:  Acta Neuropathol       Date:  1967-10-20       Impact factor: 17.088

6.  Experimental studies on the pathogenesis of leucodystrophies. I. The effect of intracerebrally injected sphingolipids in the rat's brain.

Authors:  Y Olsson; P Sourander; L Svennerholm
Journal:  Acta Neuropathol       Date:  1966-03-04       Impact factor: 17.088

7.  Sphingolipids and their precursors in human brain (normal and MS).

Authors:  B Gerstl; M G Tavaststjerna; L F Eng; J K Smith
Journal:  Z Neurol       Date:  1972

8.  Fatty acid composition of cerebrosides and cerebroside sulphatides in cerebral oedema.

Authors:  T Yanagihara; J N Cumings
Journal:  Acta Neuropathol       Date:  1968-12-18       Impact factor: 17.088

9.  Fatty acid composition of free ceramides of kidney and cerebellum from a patient with Farber's disease.

Authors:  M Sugita; P Connolly; J T Dulaney; H W Moser
Journal:  Lipids       Date:  1973-07       Impact factor: 1.880

10.  The fatty acid composition of major glycosphingolipids (cerebrosides and sulfatides) in human cerebral white matter measured by a simple micromethod.

Authors:  R Heipertz; H Pilz; W Scholz
Journal:  J Neurol       Date:  1976-07-15       Impact factor: 4.849

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