TY - JOUR T1 - Oxidative Bioactivation of the Lactol Prodrug of A Lactone Cyclooxygenase-2 Inhibitor JF - Drug Metabolism and Disposition JO - Drug Metab Dispos SP - 403 LP - 409 VL - 27 IS - 3 AU - Deborah A. Nicoll-Griffith AU - Jean-Pierre Falgueyret AU - José M. Silva AU - Pierre-Emmanuel Morin AU - Laird Trimble AU - Chi-C. Chan AU - Sophie Clas AU - Serge Leger AU - Zhaoyin Wang AU - James A. Yergey AU - Denis Riendeau Y1 - 1999/03/01 UR - http://dmd.aspetjournals.org/content/27/3/403.abstract N2 - The lactol derivative of a lactone cyclooxygenase-2 inhibitor (DFU) was evaluated in vivo and in vitro for its potential suitability as a prodrug. DFU-lactol was found to be 10 to 20 times more soluble than DFU in a variety of aqueous vehicles. After administration of DFU-lactol at 20 mg kg−1 p.o. in rats, aCmax of 7.5 μM DFU was reached in the plasma. After oral administration, the ED50s of DFU-lactol in the carrageenan-induced paw edema and lipopolysaccharide-induced pyresis assays in rats are comparable with the ED50s observed when dosing with DFU. Incubations of DFU-lactol with rat and human hepatocytes demonstrated that the oxidation of DFU-lactol can be mediated by liver enzymes and that a competing pathway is direct glucuronidation of the DFU-lactol hydroxyl group. Assays with subcellular fractions from rat liver indicated that most of the oxidation of DFU-lactol occurs in the cytosolic fraction and requires NAD(P)+. Human liver cytosol can also support the oxidation of DFU-lactol to DFU when NAD(P)+ is added to the incubations. Fractionation of human liver cytosolic proteins showed that at least three enzymes are capable of efficiently effecting the oxidation of DFU-lactol to DFU. Incubations with commercially available dehydrogenases suggest that alcohol and hydroxysteroid dehydrogenases are involved in this oxidative process. These data together suggest that lactols may represent useful prodrugs for lactone-containing drugs. The American Society for Pharmacology and Experimental Therapeutics ER -