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Therapeutic Methods and Therapies TCIM
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1.
Arch Pharm Res ; 34(2): 229-36, 2011 Feb.
Article in English | MEDLINE | ID: mdl-21380806

ABSTRACT

Sphingomyelinase catalyzes the hydrolysis of sphingomyelin to generate ceramide, an important molecule involved in the regulation of various cellular responses. In this study, we partially purified the neutral sphingomyelinase2 (nSMase2) and identified the inhibitors, D-lyxophytosphingosine and D-arabino-phytosphingosine, which have an inhibitory effect on nSMase2 in a concentration-dependent manner. A Dixon plot of each phytosphingosines revealed their probable inhibitory pattern, i.e., apparent competitive inhibition. These compounds did not inhibit the Mg(2+)-independent neutral SMase activity, although the known nSMase2 inhibitor, GW4869, showed inhibitory effects on Mg(2+)-independent neutral SMase activity. Further, the two phytosphingosines specifically inhibited the ceramide generation regulated by nSMase2.


Subject(s)
Aniline Compounds/pharmacology , Benzylidene Compounds/pharmacology , Ceramides/metabolism , Enzyme Inhibitors/pharmacology , Sphingomyelin Phosphodiesterase/antagonists & inhibitors , Sphingosine/analogs & derivatives , Aniline Compounds/chemistry , Animals , Benzylidene Compounds/chemistry , Cattle , Dose-Response Relationship, Drug , Drug Evaluation, Preclinical , Enzyme Inhibitors/chemistry , Enzyme Inhibitors/isolation & purification , HEK293 Cells , Humans , Magnesium/metabolism , Sphingomyelins/metabolism , Sphingosine/chemistry , Sphingosine/isolation & purification , Sphingosine/pharmacology
2.
Nat Prod Commun ; 4(7): 917-20, 2009 Jul.
Article in English | MEDLINE | ID: mdl-19731592

ABSTRACT

Chemical investigation of the crude extract of a marine sponge Dysidea robusta led to the isolation of an inseparable mixture of saturated ceramides. These were identified from spectroscopic data as well as by hydrolysis followed by LC-MS analysis of the sphingosine moieties.


Subject(s)
Ceramides/chemistry , Dysidea/chemistry , Acetylation , Animals , Ceramides/isolation & purification , Chromatography, High Pressure Liquid , Magnetic Resonance Spectroscopy , Mass Spectrometry , Spectrometry, Mass, Electrospray Ionization , Sphingosine/chemistry , Sphingosine/isolation & purification
4.
Eur J Biochem ; 259(1-2): 331-8, 1999 Jan.
Article in English | MEDLINE | ID: mdl-9914511

ABSTRACT

From the edible mushroom, the basidiomycetes Agaricus bisporus and Agaricus campestris, a novel carbohydrate-homologous series of four glyco-inositol-phospho-sphingolipids, designated basidiolipids, was isolated and the constituents purified. The chemical structures of the basidiolipids were elucidated to be: Manpbeta1-2inositol1-phospho-ceramide, Galpalpha-6[Fucpalpha-2]Galpbeta-6Manpbeta-2i nositol1-phospho-ceramide, Galpalpha-6Galpalpha-6[Fucpalpha-2]Galpbeta- 6Manpbeta-2inositol1-phospho-ceramide and Galpalpha-6Galpalpha-6Galpalpha-6[Fucpalpha-2] Galpbeta-6Manpbeta-2ino sitol1-phospho-ceramide. All four glycolipids contained a ceramide which was composed of phytosphingosine and predominantly alpha-hydroxy-behenic and alpha-hydroxy-lignoceric acid.


Subject(s)
Agaricus/chemistry , Ceramides/chemistry , Inositol Phosphates/isolation & purification , Phospholipids/chemistry , Sphingosine/analogs & derivatives , Adjuvants, Immunologic/chemistry , Carbohydrate Sequence , Fatty Acids/chemistry , Hydroxy Acids/chemistry , Molecular Sequence Data , Nuclear Magnetic Resonance, Biomolecular , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization , Sphingosine/isolation & purification
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