, Volume 4, Issue 1, pp 18–61

Molecular targets for antiepileptic drug development

  • Brian S. Meldrum
  • Michael A. Rogawski

DOI: 10.1016/j.nurt.2006.11.010

Cite this article as:
Meldrum, B.S. & Rogawski, M.A. Neurotherapeutics (2007) 4: 18. doi:10.1016/j.nurt.2006.11.010


This review considers how recent advances in the physiology of ion channels and other potential molecular targets, in conjunction with new information on the genetics of idiopathic epilepsies, can be applied to the search for improved antiepileptic drugs (AEDs). Marketed AEDs predominantly target voltage-gated cation channels (the α subunits of voltage-gated Na+ channels and also T-type voltage-gated Ca2+ channels) or influence GABA-mediated inhibition. Recently, α2-δ voltage-gated Ca2+ channel subunits and the SV2A synaptic vesicle protein have been recognized as likely targets. Genetic studies of familial idiopathic epilepsies have identified numerous genes associated with diverse epilepsy syndromes, including genes encoding Na+ channels and GABAA receptors, which are known AED targets. A strategy based on genes associated with epilepsy in animal models and humans suggests other potential AED targets, including various voltage-gated Ca2+ channel subunits and auxiliary proteins, A- or M-type voltage-gated K+ channels, and ionotropic glutamate receptors. Recent progress in ion channel research brought about by molecular cloning of the channel subunit proteins and studies in epilepsy models suggest additional targets, including G-protein-coupled receptors, such as GABAB and metabotropic glutamate receptors; hyperpolarization-activated cyclic nucleotide-gated cation (HCN) channel subunits, responsible for hyperpolarization-activated currentIh; connexins, which make up gap junctions; and neurotransmitter transporters, particularly plasma membrane and vesicular transporters for GABA and glutamate. New information from the structural characterization of ion channels, along with better understanding of ion channel function, may allow for more selective targeting. For example, Na+ channels underlying persistent Na+ currents or GABAA receptor isoforms responsible for tonic (extrasynaptic) currents represent attractive targets. The growing understanding of the pathophysiology of epilepsy and the structural and functional characterization of the molecular targets provide many opportunities to create improved epilepsy therapies.

Key Words

Epilepsy channelopathy antiepileptic drug sodium channel calcium channel potassium channel GABA receptor glutamate receptor GABA transporter glutamate transporter gap junction 

Copyright information

© The American Society for Experimental NeuroTherapeutics, Inc. 2007

Authors and Affiliations

  • Brian S. Meldrum
    • 1
  • Michael A. Rogawski
    • 2
  1. 1.Centre for Neuroscience, Division of Biomedical and Health Sciences, School of MedicineKings CollegeLondonUK
  2. 2.Epilepsy Research Section, National Institute of Neurological Disorders and StrokeNational Institutes of HealthBethesda
  3. 3.Department of NeurologyUniversity of California, DavisSacramento

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