Title of article :
NO-releasing NSAIDs are caspase inhibitors
Author/Authors :
Stefano Fiorucci، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2001
Pages :
4
From page :
232
To page :
235
Abstract :
Nitrosation of thiol-containing proteins is a mechanism for cell regulation. Nitric-oxide-releasing nonsteroidal anti-inflammatory drugs (NO-NSAIDs) are chemical entities obtained by adding a nitroxybutyl moiety to a conventional NSAID. NO-NSAIDs inhibit inflammation via cyclo-oxygenase (COX)-dependent and -independent effects. Similarly to endogenous NO, NO-NSAIDs are potent inhibitors of T helper1 (Th1) type cytokines. This effect is largely owing to post-translational nitrosation and therefore inactivation of cysteine proteases, such as the interleukin (IL)-1β converting enzyme (ICE/caspase-1) involved in pro-cytokine processing.
Journal title :
Trends in Immunology
Serial Year :
2001
Journal title :
Trends in Immunology
Record number :
468251
Link To Document :
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