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
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.