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. Author manuscript; available in PMC: 2013 Apr 1.
Published in final edited form as: Nat Rev Neurosci. 2012 Oct;13(10):675–686. doi: 10.1038/nrn3335

Figure 1. Distinctive features of synaptic kainate receptors.

Figure 1

a | Synaptic kainate receptors mediate smaller amplitude currents with much slower kinetics than AMPA receptors. Traces from recordings of synaptic currents at mossy fibre–CA3 synapses in the hippocampus show a mixed AMPA and kainate receptor-mediated excitatory postsynaptic current (EPSCAMPA–KA; black), which is predominantly mediated by AMPA receptors, the low-amplitude pharmacologically isolated EPSCKA (grey), and the peak-scaled EPSCKA (red), which illustrates the relatively slow kinetics of kainate receptors. b | Repetitive activation of pharmacologically isolated mossy fibre kainate receptors (at 20 Hz in the example) results in EPSCKA summation and increases the total charge transferred during the synaptic currents. c | Excitatory postsynaptic potentials (EPSPs) recorded during a train of mossy fibre stimulation exhibit a tonic depolarization ‘envelope’ that is contributed to by the activation of kainate receptors. This is evident in the example traces as the difference between EPSPAMPA–KA (black) and EPSPAMPA (blue) recorded in the presence of the selective postsynaptic kainate receptor antagonist UBP310 (REF. 29). d | Incorporation of the GluK4 and GluK5 subunits shape postsynaptic kainate receptor responses. The left panel shows example traces of EPSCsKA recorded from CA3 pyramidal cells following stimulation of mossy fibre projections from wild-type (black) and GluK4−/− (blue) mice (A. Contractor, unpublished results). The right panel shows that under the same recording conditions as in the previous experiment, the EPSCKA at this synapse exhibits faster kinetics in GluK5−/− mice (green) than in wild-type mice (black)46. Parts a and d (right panel) are modified, with permission, from REF. 46 © (2003) Society for Neuroscience. Part b is modified, with permission, from REF. 126 © (2007) Society for Neuroscience. Part c is modified, with permission, from REF. 29 © (2012) Oxford University Press.