Kainate receptors mediate a slow postsynaptic current in hippocampal CA3 neurons

Pablo E. Castillo, Robert C. Malenka and Roger A. Nicoll ()
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Pablo E. Castillo: University of California at San Francisco
Robert C. Malenka: ‡Physiology and Psychiatry, University of California at San Francisco
Roger A. Nicoll: University of California at San Francisco

Nature, 1997, vol. 388, issue 6638, 182-186

Abstract: Abstract Glutamate, the neurotransmitter at most excitatory synapses in the brain, activates a variety of receptor subtypes that can broadly be divided into ionotropic (ligand-gated ion channels) and metabotropic (G-protein-coupled) receptors. Ionotropic receptors mediate fast excitatory synaptic transmission, and based on pharmacological and molecular biological studies are divided into NMDA and non-NMDA subtypes. The non-NMDA receptor group is further divided into AMPA and kainate subtypes1. Virtually all fast excitatory postsynaptic currents studied so far in the central nervous system are mediated by the AMPA and NMDA subtypes of receptors. Surprisingly, despite extensive analysis of their structure, biophysical properties and anatomical distribution, a synaptic role for kainate receptors in the brain has not been found2. Here we report that repetitive activation of the hippocampal mossy fibre pathway, which is associated with high-affinity kainate binding3 and many of the kainate receptor subtypes4,5,6,7,8, generates a slow excitatory synaptic current with all of the properties expected of a kainate receptor. This activity-dependent synaptic current greatly augments the excitatory drive of CA3 pyramidal cells.

Date: 1997
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DOI: 10.1038/40645

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