| Literature DB >> 2826682 |
K Domańska-Janik1, B Gajkowska, B de Néchaud, J M Bourre.
Abstract
A disorder of CNS myelination was found in paralytic tremor ("pt") rabbits. The condition is inherited in a sex-linked recessive mode. Ultrastructurally, an obvious myelin deficiency with aberration of myelin sheath formation is observed. The yield of myelin isolation was reduced to 20-30% of control. Myelin isolated from 4-week-old "pt" rabbits contained reduced amounts of galactosphingolipids and of several myelin protein markers. Moreover, myelin basic protein, analyzed by two-dimensional gel electrophoresis, showed a deficit in its more basic components. All these facts suggest a delay in myelin maturation. Ganglioside content was increased as well as Na+,K+-ATPase specific activity. 2',3'-Cyclic nucleotide phosphodiesterase (CNPase) specific activity was the same in "pt" as in control myelin but differed by having greater sensitivity to detergent activation.Entities:
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Year: 1988 PMID: 2826682 DOI: 10.1111/j.1471-4159.1988.tb13238.x
Source DB: PubMed Journal: J Neurochem ISSN: 0022-3042 Impact factor: 5.372