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Identification and evaluation of neutral sphingomyelinase 2 inhibitors
Ist Teil von
Archives of Pharmacal Research, 2011, 34(2), , pp.229-236
Ort / Verlag
Heidelberg: Pharmaceutical Society of Korea
Erscheinungsjahr
2011
Quelle
MEDLINE
Beschreibungen/Notizen
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
-
lyxo
phytosphingosine 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.