SPHINGOLIPID METABOLIC DISORDERS IN TREMBLER MOUSE PERIPHERAL-NERVES IN-VIVO RESULT FROM AN ABNORMAL SUBSTRATE SUPPLY

Citation
Am. Heape et al., SPHINGOLIPID METABOLIC DISORDERS IN TREMBLER MOUSE PERIPHERAL-NERVES IN-VIVO RESULT FROM AN ABNORMAL SUBSTRATE SUPPLY, Journal of neurochemistry, 65(4), 1995, pp. 1665-1673
Citations number
21
Categorie Soggetti
Biology,Neurosciences
Journal title
ISSN journal
00223042
Volume
65
Issue
4
Year of publication
1995
Pages
1665 - 1673
Database
ISI
SICI code
0022-3042(1995)65:4<1665:SMDITM>2.0.ZU;2-A
Abstract
Sphingolipid metabolic pathways in the peripheral nerves of dysmyelina ting Trembler mice were studied in vivo, using intraneurally injected [H-3]palmitate as the exogenous substrate. The kinetic analysis of the experimental data obtained for the mutant revealed that, as in normal nerves, two metabolically and kinetically independent pathways are im plicated in the biosynthesis of the major peripheral nerve sphingolipi ds: the ceramide pathway and another pathway in which there is no dete ctable labeled intermediate (''direct amidification''), The results al so show that, in the Trembler mouse sciatic nerves: (a) The severely d eficient sphingolipid biosynthesis results from the constitution of a qualitatively and quantitatively abnormal fatty acid substrate pool de stined for metabolism via the ceramide pathway, which ensures the tota lity of the galactocerebroside labeling and two-thirds of that of sphi ngomyelin, The ceramide intermediates of this pathway are labeled only on their fatty acyl moiety, which contains only 16-carbon atom chains , (b) ''Direct amidification'' events implicated in sphingolipid label ing are decreased compared with normal and account for the remaining s phingomyelin formation.