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      Felbamate but not phenytoin or gabapentin reduces glutamate release by blocking presynaptic NMDA receptors in the entorhinal cortex

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          Summary

          We have shown that a number of anticonvulsant drugs can reduce glutamate release at synapses in the rat entorhinal cortex (EC) in vitro. We have also shown that presynaptic NMDA receptors (NMDAr) tonically facilitate glutamate release at these synapses. In the present study we determined whether, phenytoin, gabapentin and felbamate may reduce glutamate release by blocking the presynaptic NMDAr. Whole cell patch clamp recordings of spontaneous excitatory postsynaptic currents (sEPSCs) were used as a monitor of presynaptic glutamate release. Postsynaptic NMDAr were blocked with internal dialysis with an NMDAr channel blocker. The antagonist, 2-AP5, reduced the frequency of sEPSCs by blocking the presynaptic facilitatory NMDAr, but did not occlude a reduction in sEPSC frequency by gabapentin or phenytoin. Felbamate also reduced sEPSC frequency, but this effect was occluded by prior application of 2-AP5. Thus, whilst all three drugs can reduce glutamate release, only the action of felbamate seems to be due to interaction with presynaptic NMDAr.

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          Most cited references38

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          Glutamate exocytosis from astrocytes controls synaptic strength.

          The release of transmitters from glia influences synaptic functions. The modalities and physiological functions of glial release are poorly understood. Here we show that glutamate exocytosis from astrocytes of the rat hippocampal dentate molecular layer enhances synaptic strength at excitatory synapses between perforant path afferents and granule cells. The effect is mediated by ifenprodil-sensitive NMDA ionotropic glutamate receptors and involves an increase of transmitter release at the synapse. Correspondingly, we identify NMDA receptor 2B subunits on the extrasynaptic portion of excitatory nerve terminals. The receptor distribution is spatially related to glutamate-containing synaptic-like microvesicles in the apposed astrocytic processes. This glial regulatory pathway is endogenously activated by neuronal activity-dependent stimulation of purinergic P2Y1 receptors on the astrocytes. Thus, we provide the first combined functional and ultrastructural evidence for a physiological control of synaptic activity via exocytosis of glutamate from astrocytes.
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            The neurobiology of antiepileptic drugs.

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              Differential roles of NR2A and NR2B-containing NMDA receptors in cortical long-term potentiation and long-term depression.

              It is widely believed that long-term depression (LTD) and its counterpart, long-term potentiation (LTP), involve mechanisms that are crucial for learning and memory. However, LTD is difficult to induce in adult cortex for reasons that are not known. Here we show that LTD can be readily induced in adult cortex by the activation of NMDA receptors (NMDARs), after inhibition of glutamate uptake. Interestingly there is no need to activate synaptic NMDARs to induce this LTD, suggesting that LTD is triggered primarily by extrasynaptic NMDA receptors. We also find that de novo LTD requires the activation of NR2B-containing NMDAR, whereas LTP requires activation of NR2A-containing NMDARs. Surprisingly another form of LTD, depotentiation, requires activation of NR2A-containing NMDARs. Therefore, NMDARs with different synaptic locations and subunit compositions are involved in various forms of synaptic plasticity in adult cortex.
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                Author and article information

                Journal
                Epilepsy Res
                Epilepsy Res
                Epilepsy Research
                Elsevier Science Publishers
                0920-1211
                1872-6844
                December 2007
                December 2007
                : 77
                : 2-3
                : 157-164
                Affiliations
                Department of Pharmacy and Pharmacology, University of Bath, Claverton Down, Bath BA2 7AY, UK
                Author notes
                [* ]Corresponding author. Tel.: +44 1225 383935; fax: +44 1225 386114. r.s.g.jones@ 123456bath.ac.uk
                Article
                EPIRES3870
                10.1016/j.eplepsyres.2007.09.005
                2496957
                17980555
                e9d3ab9d-8b4e-4356-a934-c7563a7ba71d
                © 2007 Elsevier B.V.

                This document may be redistributed and reused, subject to certain conditions.

                History
                : 23 May 2007
                : 4 September 2007
                : 11 September 2007
                Categories
                Short Communication

                Neurology
                phenytoin,entorhinal cortex,felbamate,glutamate release,presynaptic nmda receptors,gabapentin

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