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Stereoselective inhibition of rat brain cyclooxygenase by dexketoprofen
Author(s) -
Carabaza Assumpta,
Cabré Francesc,
García Ana M.,
Rotllan Elisabet,
García M. Luisa,
Mauleón David
Publication year - 1997
Publication title -
chirality
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.43
H-Index - 77
eISSN - 1520-636X
pISSN - 0899-0042
DOI - 10.1002/(sici)1520-636x(1997)9:3<281::aid-chir13>3.0.co;2-j
Subject(s) - ketoprofen , chemistry , enantiomer , cyclooxygenase , prostaglandin , pharmacology , analgesic , ic50 , microsome , stereoselectivity , stereochemistry , alpha (finance) , enzyme , biochemistry , in vitro , chromatography , biology , medicine , catalysis , construct validity , nursing , patient satisfaction
Although it has been assumed that the effects of nonsteroidal antiinflammatory drugs (NSAIDs) are mainly the result of their action on local synthesis of prostaglandins, there is growing evidence to suggest that they may also exert a central analgesic action. Some authors have suggested that inhibition of prostaglandin synthesis in the brain could contribute to the analgesic action. The effect of dexketoprofen trometamol (tromethamine salt of the enantiomer (+)‐S‐ketoprofen) on prostaglandin synthesis was investigated in rat brain fragments and in cyclooxygenase preparations from rat brain microsomes. Effects of the (‐)‐R‐enantiomer and the racemic mixture were also evaluated. Significant levels of prostaglandin F 2α (PGF 2α ) were synthesized in rat brain fragments after 10 min of incubation at 37°C. Dexketoprofen was found to be a potent inhibitor of this PGF 2α production in rat brain (IC 50 = 6.2 n M ), and it completely suppressed PGF 2α production at 1 μ M concentration. In addition, inhibition of PGF 2α synthesis by dexketoprofen was highly stereoselective since the enantiomer (‐)‐R‐ketoprofen was significantly less potent (IC 50 = 294 n M ); with this enantiomer, even at high concentrations such as 1 μ M , less than 60% inhibition was achieved. These results correlated with those obtained in the study of racemic ketoprofen and its enantiomers on cyclooxygenase activity of rat brain microsomes, where dexketoprofen also inhibited enzymatic activity stereoselectively. IC 50 values obtained for dexketoprofen, (‐)‐R‐ketoprofen, and rac ‐ketoprofen were 3.5 μ M , 45.3 μ M , and 5.8 μ M , respectively. The above results could be related to the potent analgesic effect of dexketoprofen observed in vivo, which was also stereoselective. Taken together, these findings suggest that prostaglandin synthesis inhibition in rat brain by dexketoprofen could be associated, at least in part, with the analgesic effect of this NSAID. Chirality 9:281–285, 1997. © 1997 Wiley‐Liss, Inc.