Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Sphingomyelin, metabolites

Auge, N., Negre-Salvayre, A., Salayre, R., Levade, T. 2000. Sphingomyelin metabolites in vascular cell signalling and atherogenesis. Prog. Lipid Res. 39, 207-229. [Pg.668]

Vivekananda, J., Smith, D., and King, R.J. (2001). Sphingomyelin metabolites inhibit sphingomyelin S3mthase and CTP phosphocholine cytidylyltransferase. Am J Physiol Lung Cell Mol Physiol 281, L98-107. [Pg.291]

Alessenko, A.V., 2000, The role of sphingomyelin cycle metabolites in transduction of signals of ceU prohferation, differentiation and death, Memb. Cell Biol. 13 303-320. [Pg.260]

Hormonal lipids. We have already considered a number of hormones that are not water-soluble but may have to be transported by carrier proteins to their sites of action. These include retinoic acid (Box 22-A), metabolites of vitamin D (Box 22-C), and the plateletactivating factor (Box 8-A). The last functions in the brain311 as well as in blood. Hormonal lipids also include the prostaglandins (Fig. 21-7), leukotrienes, and lipoxins (Fig. 21-8). These are products of the eicosenoid cascade or network, which is activated by receptors linked to phospholipase C (Fig. 11-9). Cera-mide formed by hydrolysis of sphingomyelin initiates... [Pg.1757]

Fatty Acids Can Inhibit SREBP via Metabolites of Sphingomyelin... [Pg.375]

Fig. 8. Head-group additions to ceramide in a schematic representation. Starting with a given molecular subspecies of ceramide (Fig. 7), head groups can be added to make sphingomyelin by addition of a phospho-choline moiety (by transesterification from phosphatidylcholine), phosphate (from ATP), glucose (from UDP-Glc), galactose (from UDP-Gal), or a fatty acid (by transacylation from phosphatidylcholine or phosphatidylethanolamine). Subsequent metabolites are formed by sequential carbohydrate addition (from UDP-sugars except for GDP-fucose, GDP-mannose and CMP-sialic acid) or addition of sulfate. Fig. 8. Head-group additions to ceramide in a schematic representation. Starting with a given molecular subspecies of ceramide (Fig. 7), head groups can be added to make sphingomyelin by addition of a phospho-choline moiety (by transesterification from phosphatidylcholine), phosphate (from ATP), glucose (from UDP-Glc), galactose (from UDP-Gal), or a fatty acid (by transacylation from phosphatidylcholine or phosphatidylethanolamine). Subsequent metabolites are formed by sequential carbohydrate addition (from UDP-sugars except for GDP-fucose, GDP-mannose and CMP-sialic acid) or addition of sulfate.
Denisova, N.A., Fisher, D., Provost, M. Joseph, J.A. (1999). The role of glutathione, membrane sphingomyelin, and its metabolites in oxidative stress-induced calcium dysregulation in PC 12 cells. Free Radical Biology and Medicine, 27,1292-1301. [Pg.292]

Thin-layer chromatography can be used for the separation of drugs, amino acids, sugars and catecholamine metabolites, and for the determination of lecithin-sphingomyelin ratios. [Pg.341]


See other pages where Sphingomyelin, metabolites is mentioned: [Pg.44]    [Pg.299]    [Pg.58]    [Pg.327]    [Pg.341]    [Pg.121]    [Pg.27]    [Pg.44]    [Pg.1763]    [Pg.1769]    [Pg.1675]    [Pg.221]    [Pg.196]    [Pg.381]    [Pg.365]    [Pg.389]    [Pg.136]    [Pg.310]    [Pg.281]    [Pg.282]    [Pg.600]    [Pg.237]    [Pg.273]    [Pg.158]    [Pg.287]    [Pg.411]    [Pg.62]    [Pg.408]   
See also in sourсe #XX -- [ Pg.375 ]




SEARCH



Sphingomyeline

Sphingomyelins

© 2024 chempedia.info