A kainate receptor is an ionotropic receptor activated by the neurotransmitter glutamate. Activation opens an ion channel, coupling chemical recognition to an electrical response. The family is named after kainic acid, an experimental agonist. Kainate receptors and AMPA receptors are distinct receptor families even though some experimental agonists can activate both, making pharmacological responses alone difficult to interpret.[ref]
Altered synaptic physiology and reduced susceptibility to kainate-induced seizures in GluR6-deficient mice by C. Mulle and others. Abstract: ionotropic receptor classes and difficulty separating kainate from AMPA responses.
A genetic experiment helped isolate the kainate component. C. Mulle and colleagues generated mice lacking the subunit then called GluR6. Neurons in the hippocampal CA3 region became much less sensitive to kainic acid; a postsynaptic kainate current evoked by a train of mossy-fibre stimulation was absent in the mutants. This linked a molecular subunit to a synaptically evoked response, rather than merely to a response produced by bathing tissue in an agonist.[ref]
Altered synaptic physiology and reduced susceptibility to kainate-induced seizures in GluR6-deficient mice by C. Mulle and others. Nature392,601–605(1998), abstract: deletion, CA3 responses and mossy-fibre stimulation.
The subunit's current name is GluK2.[ref]https://www.ncbi.nlm.nih.gov/mesh/2106638. NLM GluK2 nomenclature record, entry terms include GluR6
For example, a current produced by an agonist that also activates AMPA receptors cannot be assigned wholly to kainate receptors. Comparing selective perturbations with synaptic stimulation supplies stronger evidence for the receptor responsible. In another experimental setting, paired recordings in ground-squirrel retina showed that AMPA receptors and kainate receptors could route cone signals into OFF retinal bipolar cells with different temporal filtering properties.[ref]
Bipolar cells use kainate and AMPA receptors to filter visual information into separate channels by S. H. DeVries. Abstract and Results: paired cone/bipolar recordings, pharmacology and distinct temporal filtering.
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