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Article
January 1967

Gangliosides and Glycerophospholipids in Multiple Sclerosis White Matter

Author Affiliations

ANN ARBOR, MICH
From the Mental Health Research Institute and Department of Neurology, University of Michigan, Ann Arbor, Mich.

Arch Neurol. 1967;16(1):44-54. doi:10.1001/archneur.1967.00470190048006
Abstract

HISTOLOGICALLY, multiple sclerosis is characterized by focal necrobiosis of white matter with degeneration of myelin sheaths and, usually, a high degree of sparing of axons.1 Chemically, the foci of demyelination show loss of glycerophospholipids, cholesterol, and cerebrosides,2-6 as well as selective loss of particular fatty acids.5-8 The chemical changes are consistent with the histological demonstration of myelin loss but are not sufficiently specific to indicate whether the axons passing through the plaques are normal in composition.

The lipid most characteristic of gray matter, gangliosides, has not been studied with modern methods in multiple sclerosis plaques or normal-appearing white matter (NAWM). Probably the main reason for this is the difficulty of adapting the analytical techniques to determining the relatively low concentration of gangliosides in white matter. Lowden and Wolfe,9 in a detailed study of the distribution of lipid-bound sialic acid, concluded that gangliosides occur in

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