Stereoselective Analysis of the Antiseizure Activity of Fenfluramine and Norfenfluramine in Mice: Is -Norfenfluramine a Better Follow-Up Compound to Racemic-Fenfluramine?

The aim of this study was to investigate the comparative antiseizure activity of the -enantiomers of ,-fenfluramine and ,-norfenfluramine and to evaluate the relationship between their concentration in plasma and brain and anticonvulsant activity. ,-Fenfluramine, ,-norfenfluramine and their individual enantiomers were evaluated in the mouse maximal electroshock seizure (MES) test. ,-Fenfluramine, ,-norfenfluramine and their individual -enantiomers were also assessed in the DBA/2 mouse audiogenic seizure model. All compounds were administered intraperitoneally. Brain and plasma concentrations of the test compounds in DBA/2 mice were quantified and correlated with anticonvulsant activity. In the MES test, fenfluramine, norfenfluramine and their enantiomers showed comparable anticonvulsant activity, with ED values between 5.1 and 14.8 mg/kg. In the audiogenic seizure model, -norfenfluramine was 9 times more potent than ,-fenfluramine and 15 times more potent than -fenfluramine based on ED (1.2 vs. 10.2 and 17.7 mg/kg, respectively). Brain concentrations of all compounds were about 20-fold higher than in plasma. Based on brain EC values, -norfenfluramine was 7 times more potent than ,-fenfluramine and 13 times more potent than -fenfluramine (1940 vs. 13,200 and 25,400 ng/g, respectively). EC values for metabolically formed ,-norfenfluramine and -norfenfluramine were similar to brain EC values of the same compounds administered as such, suggesting that, in the audiogenic seizure model, the metabolites were responsible for the antiseizure activity of the parent compounds. Because of the evidence linking -norfenfluramine to ,-fenfluramine to cardiovascular and metabolic adverse effects, their -enantiomers could potentially be safer follow-up compounds to ,-fenfluramine. We found that, in the models tested, the activity of -fenfluramine and -norfenfluramine was comparable to that of the corresponding racemates. Based on the results in DBA/2 mice and other considerations, -norfenfluramine appears to be a particularly attractive candidate for further evaluation as a novel, enantiomerically pure antiseizure medication.