期刊
CEREBRAL CORTEX
卷 23, 期 2, 页码 323-331出版社
OXFORD UNIV PRESS INC
DOI: 10.1093/cercor/bhs022
关键词
hippocampus; kainate receptors; synapse; synaptic integration; temporal lobe epilepsy
资金
- Centre National de la Recherche Scientifique
- Fondation pour la Recherche Medicale
- Conseil Regional d'Aquitaine
- European Commission (EUSynapse Project) [M-CT-2005-019055]
- Nationale de la Recherche
Progress in understanding the roles of kainate receptors (KARs) in synaptic integration, synaptic networks, and higher brain function has been hampered by the lack of selective pharmacological tools. We have found that UBP310 and related willardiine derivatives, previously characterized as selective GluK1 and GluK3 KAR antagonists, block postsynaptic KARs at hippocampal mossy fiber (MF) CA3 synapses while sparing AMPA and NMDA receptors. We further show that UBP310 is an antagonist of recombinant GluK2/GluK5 receptors, the major population of KARs in the brain. Postsynaptic KAR receptor blockade at MF synapses significantly reduces the sustained depolarization, which builds up during repetitive activity, and impacts on spike transmission mediated by heterosynaptic signals. In addition, KARs present in aberrant MF synapses in the epileptic hippocampus were also blocked by UBP310. Our results support a specific role for postsynaptic KARs in synaptic integration of CA3 pyramidal cells and describe a tool that will be instrumental in understanding the physiopathological role of KARs in the brain.
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