Bacterial conversion of cholesterol into coprostanol independent of cerebrosides in the medium.
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Glucocerebroside and galactocerebroside increased the respiratory rate of liver and brain mitochondria by 33-400% and produced an average 30% decrease in oxidative phosphorylation. Psychosine stimulated mitochondrial respiration 66-700%. At concentrations over 100 micrograms/mg mitochondrial protein, oxidative phosphorylation was completely inhibited. Atractyloside did not prevent the respiratory stimulation. Ca2+ transport was blocked and addition of ATP could not overcome this inhibition. The possible deleterious effect of glycosphingolipids on the conformation of the mitochondrial membrane and cellular bioenergetics is discussed in relation to the toxicity of accumulating glycosphingolipids in Gaucher and Krabbe diseases.
PURPOSE: To measure the effect of the major lipid components of white matter on the relaxation times and magnetization transfer (MT) of water protons. MATERIALS AND METHODS: Multilamellar vesicle (MLV) suspensions of pure phosphatidylcholine (PC) and PC with varying proportions of cholesterol (CHOL), sphingomyelin (SPH), and galactocerebroside (GC) were produced at varying pH. T1, T2, and MT were measured. RESULTS: Suspensions consisting of PC with CHOL or SPH caused greater shortening of T1 and T2 and slightly greater MT effects than did PC alone. Suspensions consisting of GC and PC caused the greatest decrease in relaxation times, and the MT effect was two to three times greater than with either CHOL-PC or SPH-PC suspensions. At acidic pH, the relaxation time changes and the MT effects with CHOL-PC, SPH-PC, and GC-PC suspensions were greater than the effects of the same MLVs at physiologic pH. CONCLUSION: GC has the strongest effect on relaxivity and MT of all the major white matter lipids. The relaxivity and MT observed with white matter lipids is pH dependent, indicating that chemical exchange of protons likely contributes to relaxivity and MT.
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This investigation was conducted to determine whether or not plasma galactosyl ceramides were elevated in patients with stroke and multiple sclerosis, and to determine glycosyl ceramide concentrations in older, normal subjects. It was hypothesized that central nervous system destruction, like that which occurs in stroke or in the demyelination characteristic of multiple sclerosis, might be reflected by changes in plasma glycosyl ceramides, specifically by an increased percentage of galactosyl ceramide. Glycosyl ceramides were analyzed in duplicate 10 ml aliquots of plasma from each of seven patients with stroke, five patients with multiple sclerosis and five control subjects age-matched with stroke patients. Mean percentages of galactosyl ceramide for both controls (11.06 percent) and multiple sclerosis (11.40 percent) were strikingly similar. The percent of galactosyl ceramides for stroke was slightly elevated (14.32 percent) but there were no significant differences at the p=greater than 0.05 level.