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- Title
Effects of pyrrophenone, an inhibitor of group IVA phospholipase A2, on eicosanoid and PAF biosynthesis in human neutrophils.
- Authors
Flamand, N.; Picard, S.; Lemieux, L.; Pouliot, M.; Bourgoin, S. G.; Borgeat, P.
- Abstract
Background and Purpose:The biosynthesis of leukotrienes (LT) and platelet-activating factor (PAF) involves the release of their respective precursors, arachidonic acid (AA) and lyso-PAF by the group IVA PLA2 (cPLA2α). This paper aims at characterizing the inhibitory properties of the cPLA2α inhibitor pyrrophenone on eicosanoids and PAF in human neutrophils (PMN).Experimental Approach:Freshly isolated human PMN were activated with physiological and pharmacological agents (fMLP, PAF, exogenous AA, A23187 and thapsigargin) in presence and absence of the cPLA2α inhibitor pyrrophenone and biosynthesis of LT, PAF, and PGE2 was measured.Key Results:Pyrrophenone potently inhibited LT, PGE2 and PAF biosynthesis in PMN with IC50s in the range of 1–20 nM. These inhibitory effects of pyrrophenone were specific (the consequence of substrate deprivation), as shown by the reversal of inhibition by exogenous AA and lyso-PAF. Comparative assessment of pyrrophenone, methyl-arachidonoyl-fluoro-phosphonate (MAFP) and arachidonoyl-trifluoromethylketone (AACOCF3) demonstrated that pyrrophenone was more specific and 100-fold more potent than MAFP and AACOCF3 for the inhibition of LT biosynthesis in A23187-activated PMN. The inhibitory effect of pyrrophenone on LT biosynthesis was reversible as LT biosynthesis was recovered when pyrrophenone-treated PMN were washed with autologous plasma. No alteration of phospholipase D (PLD) activity in fMLP-activated PMN was observed with up to 10 μM pyrrophenone, suggesting that the cPLA2α inhibitor does not directly inhibit PLD.Conclusions and Implications:Pyrrophenone is a more potent and specific cPLA2α inhibitor than MAFP and AACOCF3 and represents an excellent pharmacological tool to investigate the biosynthesis and the biological roles of eicosanoids and PAF.British Journal of Pharmacology (2006) 149, 385–392. doi:10.1038/sj.bjp.0706879; published online 11 September 2006
- Subjects
PHARMACEUTICAL research; PHARMACOLOGY; ENZYME inhibitors; PHOSPHOLIPASE A2; EICOSANOIDS; INFLAMMATORY mediators; PLATELET activating factor; BIOSYNTHESIS; NEUTROPHILS
- Publication
British Journal of Pharmacology, 2006, Vol 149, Issue 4, p385
- ISSN
0007-1188
- Publication type
journal article
- DOI
10.1038/sj.bjp.0706879