a type of
glutamate receptor that binds NMDA as well as glutamate. NMDA receptors are coupled to
ligand-gated ion channels and are also voltage-sensitive, which enables them to participate in a variety of information-processing operations at synapses where glutamate is the neurotransmitter. The drugs of abuse
ketamine and
PCP are antagonists at NMDA receptors, preventing the influx of calcium ions at
calcium channels, which may cause the hallucinogenic effects of these drugs. Excessive flow of calcium ions into the presynaptic neuron via the NMDA receptor is thought to contribute to glutamate toxicity. A hypothesis on the etiology of schizophrenia involves dysfunction of the NMDA glutamate receptor (see
glutamate hypothesis). Compare
AMPA receptor.