Mutual inversion of flurbiprofen enantiomers in various rat and mouse strains |
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| Authors: | Natasja de Bruin Nerea Ferreirós Mike Schmidt Martine Hofmann Carlo Angioni Gerd Geisslinger Michael John Parnham |
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| Affiliation: | 1. Fraunhofer Institute for Molecular Biology and Applied Ecology IME, Research Center for Translational Medicine and Pharmacology TMP, Industriepark H?chst, Frankfurt am Main, Germany;2. Pharmazentrum Frankfurt/ZAFES, Institute of Clinical Pharmacology, Goethe‐University Frankfurt, Frankfurt am Main, Germany |
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| Abstract: | Flurbiprofen (F) is a nonsteroidal anti‐inflammatory drug (NSAID) used therapeutically as the racemate of (R)‐enantiomer and (S)‐enantiomer. The inversion of RF to SF and vice versa was investigated in C57Bl/6 and SJL mice and Dark Agouti and Lewis rats. The enzyme α‐methylacyl‐CoA racemase (AMACR) is involved in the chiral inversion pathway that converts members of the 2‐arylpropionic acid NSAIDs from the R‐enantiomer to the S‐enantiomer. We studied C57Bl/6 mice deficient in AMACR postulating that they should show reduced inversion of RF to SF. In line with the data of others in mice, (R)‐inversion to (S)‐inversion was relatively high in both the C57Bl/6 and SJL mice (fraction inverted, FI = 37.7% and 24.7%, respectively). In contrast, in AMACR deficient mice, there was no measurable peak for SF after administration of RF. The results in both rat strains (Dark Agouti and Lewis rats, FI = 1.4% and 4.1%, respectively) confirm the low chiral inversion of the enantiomers of flurbiprofen in the rat, as observed by other authors in the Sprague‐Dawley strain (<5%). From the present results, we conclude that for the study of flurbiprofen enantiomers, the rat is more suitable than the mouse as a model for the human in which (R)‐inversion to (S)‐inversion is negligible. |
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| Keywords: | (R)‐flurbiprofen (RF) (S)‐flurbiprofen (SF) enantiomers experimental autoimmune encephalomyelitis (EAE) α ‐methylacyl‐CoA racemase (AMACR) |
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