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Journal of Pharmacology And Experimental Therapeutics Fast Forward
First published on June 18, 2008; DOI: 10.1124/jpet.108.140368


0022-3565/08/3263-966-974$20.00
JPET 326:966-974, 2008
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NEUROPHARMACOLOGY

Combination Therapy with Fenofibrate, a Peroxisome Proliferator-Activated Receptor {alpha} Agonist, and Simvastatin, a 3-Hydroxy-3-methylglutaryl-Coenzyme A Reductase Inhibitor, on Experimental Traumatic Brain Injury

Xiao Ru Chen, Valerie C. Besson, Tiphaine Beziaud, Michel Plotkine, and Catherine Marchand-Leroux

Equipe de Recherche "Pharmacologie de la Circulation Cérébrale" (EA 2510), Faculté des Sciences Pharmaceutiques et Biologiques, Université Paris Descartes, Paris, France

We and others have demonstrated that fibrates [peroxisome proliferator-activated receptor (PPAR){alpha} agonists] and statins (3-hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors) exerted neuroprotective and pleiotropic effects in experimental models of traumatic brain injury (TBI). Because the combination of statins and fibrates synergistically enhanced PPAR{alpha} activation, we hypothesized that the combination of both drugs may exert more important and/or prolonged beneficial effects in TBI than each alone. In this study, we examined the combination of fenofibrate with simvastatin, administered 1 and 6 h after injury, on the consequences of TBI. First, our dose-effect study demonstrated that the most efficient dose of simvastatin (37.5 mg/kg) reduced post-traumatic neurological deficits and brain edema. Then, the effects of the combination of fenofibrate (50 mg/kg) and simvastatin (37.5 mg/kg), given p.o. at 1 and 6 h after TBI, were evaluated on the TBI consequences in the early and late phase after injury. The combination exerted more sustained neurological recovery-promoting and antiedematous effects than monotherapies, and it synergistically decreased the post-traumatic brain lesion. Furthermore, a delayed treatment given p.o. at 3 and 8 h after TBI with the combination was still efficient on neurological deficits induced by TBI, but it failed to reduce the brain edema at 48 h. The present data represent the first demonstration that the combination of fenofibrate and simvastatin exerts prolonged and synergistic neuroprotective effects than each drug alone. Thus, these results may have important therapeutic significance for the treatment of TBI.


Received April 24, 2008; accepted June 17, 2008.

Address correspondence to: Dr. Valerie Besson, Laboratoire de Pharmacologie, EA 2510, Université Paris Descartes, 4 avenue de l'Observatoire, F-75006 Paris, France. E-mail: valerie.besson{at}univ-paris5.fr







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