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Fatty Acid and Lipid Composition of the Brain of a Myelin Deficient Mutant, the “Quaking” Mouse
Author(s) -
BAUMANN N. A.,
JACQUE C. M.,
POLLET S. A.,
HARPIN M. L.
Publication year - 1968
Publication title -
european journal of biochemistry
Language(s) - English
Resource type - Journals
eISSN - 1432-1033
pISSN - 0014-2956
DOI - 10.1111/j.1432-1033.1968.tb00216.x
Subject(s) - galactolipids , myelin , sphingomyelin , cerebroside , biology , sphingolipid , mutant , biochemistry , lipid metabolism , endocrinology , metabolism , choline , galactolipid , medicine , central nervous system , phospholipid , cholesterol , gene , chloroplast , membrane
The “Quaking” mouse is a recessive autosomal mutant characterized by a deficient myelination of the central nervous system. The disease is recognized at about the twelfth day after birth and reaches its full expression by about three weeks. The animal has an unsteady gait and a marked tremor of the hind quarters; epileptic fits are induced by sensory stimulations at the adult age. This mutation apparently involves the process of myelin formation; there is no evidence of destruction. The analysis of brain fatty acids and lipids was undertaken to find out if the myelin deficiency involves an inborn error in the metabolism of one of its major constituents. “Quaking” males aged from seven to ten weeks were compared to apparently normal litter‐mates. At this stage, myelination is achieved. Brain lipids are diminished, especially galactolipids. Qualitative modifications of cerebrosides, sphingomyelin and sulphatides have been detected by mono and two dimensional thin layer chromatography. The proportion of long chain fatty acids (especially C 24 ) is greatly diminished, as shown by gas chromatography. This is true for both cerebrosides and sphingomyelin. In conclusion, the long chain fatty acids of galactolipids and sphingomyelin are considerably diminished in the “Quaking” mouse. Whether it is a cause or a consequence of myelination deficiency remains to be proved, although the importance of the alteration is in favour of the first hypothesis.

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