NMDA Receptor GluN2A Relevant to Schizophrenia Identified

NMDA receptor GluN2C appears to decline in the brains of schizophrenia patients. NMDA receptors are the sensors in the brain critical for learning and memory.

Mice without adequate GluN2C levels were found to display abnormalities in learning, memory and sensory processing, which together resemble schizophrenia in humans. The enzyme GluN2C has a key role in ketamine mechanism, a drug being studied for its rapid anti-depressant effects.

Researchers at Emory have been probing one variety of NMDA receptor assembly found in the cerebellum, and also in the thalamus, a central gateway for sensory inputs, important for cognition, movement and sleep. This variety includes a subunit called GluN2C - together with two partners, GluN1 and GluN2A.

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Schizophrenia is a mental disorder characterized by symptoms of thought, behavior and social problems.

‘NMDA receptor GluN2C appears to decline in the brains of schizophrenia patients. NMDA receptors are the sensors in the brain critical for learning and memory.’

The results are scheduled for publication in Neuron.

Outside of a living brain, NMDA receptor assemblies are typically studied with either two copies of GluN2C or two of GluN2A, but not with one of each, says senior author Stephen Traynelis, PhD, professor of pharmacology at Emory University School of Medicine.

"Our data suggest that GluN2C is rarely by itself," Traynelis says. "It's typically paired up with another GluN2 subunit. This means we really don't know what the properties of the main NMDA receptor in the cerebellum or the thalamus are."

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Using drugs that are selective for particular combinations of NMDA receptor subunits, Traynelis' laboratory showed that an assembly of GluN2A and GluN2C is the dominant form in the cerebellum. When GluN2C is introduced into cortical neurons, it prefers to pair up with GluN2A, the researchers found. This raises the question in regions such as the thalamus of whether GluN2C also appears with a partner GluN2 subunit. They also observed that the GluN2A-GluN2C assembly has distinct electrochemical properties.

Traynelis' laboratory, working with colleagues from Emory's Department of Chemistry, has recently identified compounds that are selective for GluN2C-containing assemblies, and determined which compounds are likely to be active against GluN2C when it is paired up with GluN2A.

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"For GluN2C, we believe that the assembly that contains GluN1 and two different GluN2 subunits will be the receptor to study, whether it comes to pharmacology, biophysics, or clinical relevance," he says. Similar efforts are underway to identify the subunit composition of GluN2D-containing receptors, which may also be paired with other subunits.

Source-Eurekalert

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