TY - JOUR T1 - Interaction of the Electrophilic Ketoprofenyl-Glucuronide and Ketoprofenyl-Coenzyme A Conjugates with Cytosolic Glutathione <em>S</em>-Transferases JF - Drug Metabolism and Disposition JO - Drug Metab Dispos SP - 260 LP - 267 DO - 10.1124/dmd.107.016808 VL - 36 IS - 2 AU - Sandra Osbild AU - Jérome Bour AU - Benoît Maunit AU - Cécile Guillaume AU - Carine Asensio AU - Jean-François Muller AU - Patrick Netter AU - Glbert Kirsch AU - Denyse Bagrel AU - Françoise Lapicque AU - Eric Battaglia Y1 - 2008/02/01 UR - http://dmd.aspetjournals.org/content/36/2/260.abstract N2 - Carboxylic acid-containing drugs are metabolized mainly through the formation of glucuronide and coenzyme A esters. These conjugates have been suspected to be responsible for the toxicity of several nonsteroidal anti-inflammatory drugs because of the reactivity of the electrophilic ester bond. In the present study we investigated the reactivity of ketoprofenyl-acylglucuronide (KPF-OG) and ketoprofenyl-acyl-coenzyme A (KPF-SCoA) toward cytosolic rat liver glutathione S-transferases (GST). We observed that KPF-SCoA, but not KPF-OG inhibited the conjugation of 1-chloro-2,4-dinitrobenzene and 4-nitroquinoline N-oxide catalyzed by both purified cytosolic rat liver GST and GST from FAO and H5-6 rat hepatoma cell lines. Photoaffinity labeling with KPF-SCoA suggested that the binding of this metabolite may overlap the binding site of 4-methylumbelliferone sulfate. Furthermore, high-performance liquid chromatography and mass spectrometry analysis showed that both hydrolysis and transacylation reactions were observed in the presence of GST and glutathione. The formation of ketoprofenyl-S-acyl-glutathione could be kinetically characterized (apparent Km = 196.0 ± 70.6 μM). It is concluded that KPF-SCoA is both a GST inhibitor and a substrate of a GST-dependent transacylation reaction. The reactivity and inhibitory potency of thioester CoA derivatives toward GST may have potential implications on the reported in vivo toxicity of some carboxylic acid-containing drugs. The American Society for Pharmacology and Experimental Therapeutics ER -