SV2A protein is a broad-spectrum anticonvulsant target: Functional correlation between protein binding and seizure protection in models of both partial and generalized epilepsy

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• 作者：Rafal M. Kaminski ; Alain Matagne ; Karine Leclercq ; Michel Gillard ; Philippe Michel ; Benoit Kenda ; Patrice Talaga ; Henrik Klitgaard
• 关键词：Epilepsy ; Antiepileptic drugs ; Synaptic vesicle ; SV2A ; Mouse ; Rat
• 刊名：Neuropharmacology
• 出版年：2008
• 出版时间：March 2008
• 年：2008
• 卷：54
• 期：4
• 页码：715-720
• 全文大小：355 K

文摘

SV2A, a synaptic vesicle protein, has been recently identified as a binding target for levetiracetam (Keppra^®). The specific mechanism by which SV2A binding leads to seizure protection has not yet been fully elucidated. However, a functional correlation between SV2A binding affinity and anticonvulsant potency has been observed in the mouse audiogenic seizure model. The present study was undertaken to test whether similar correlations exist in rodent models of partial and generalized epilepsies. As expected, there was a high degree of correlation between anticonvulsant potency and SV2A binding affinity in the mouse audiogenic seizure model (r² = 0.77; p < 0.001). A similar correlation was also observed in the mouse corneal kindling (r² = 0.80; p < 0.01) and in the rat model of generalized absence epilepsy (GAERS) (r² = 0.72; p < 0.01). Moreover, there were no significant differences between the slopes and intercepts of regression lines in these models. Interestingly, the protective potencies in these three epilepsy models were also well correlated with each other. As such, protective doses of a given SV2A ligand in one model could be easily predicted based on the data obtained in another model. Taken together, these results support the concept that SV2A protein is an important target for both partial and generalized epilepsies and thereby relevant for the generation of new antiepileptic drugs with potential broad-spectrum efficacy.