Journal
EUROPEAN JOURNAL OF PHARMACOLOGY
Volume 520, Issue 1-3, Pages 70-76Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.ejphar.2005.07.029
Keywords
levetiracetam; SV2A; rat spinal cord; binding
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The novel antiepileptic drug levetiracetam ((2S-(2-oxo-1-pyrrolidinyl)butanamide, KEPPRA (R)) possesses a specific binding site in brain, which has very recently been identified as the synaptic vesicle protein SV2A. The aim of this study was to evaluate the presence of a levetiracetam binding site in the spinal cord and compare its properties to that in rat brain. We used [H-3]ucb 30889 ((2S)-2-[4-(3-azidophenyl)-2-oxopyrroli din-1-yl]butanamide), a levetiracetam analogue, to perform binding assays, photoaffinity labelling and autoradiography experiments, and revealed the presence of SV2A by Western-blot analysis. [H-3]ucb 30889 binding kinetics at 4 degrees C were biphasic and saturation binding curves were compatible with the labelling of a homogenous population of binding sites with a K-d similar to that in brain. Competition curves with ligands known to interact with levetiracetam binding sites and photolabelling experiments indicated that [H-3]ucb 30889 labels the same 90 kDa protein in both spinal cord and brain. Levetiracetam binding site was localised in the grey matter of the spinal cord and its expression was not modified in a model of neuropathic pain. This study demonstrates the presence of a specific levetiracetam binding site in the rat spinal cord, which is similar to that found in rat brain. (0 2005 Elsevier BX All rights reserved.
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