GRIA1

From WikiMD's Wellness Encyclopedia

GRIA1 is a gene that encodes the GluR1 subunit of the AMPA receptor, a type of ionotropic glutamate receptor in the human body. The AMPA receptor is a key player in the central nervous system's fast synaptic transmission.

Function[edit | edit source]

The GRIA1 gene is responsible for the production of the GluR1 subunit of the AMPA receptor. This receptor is a ligand-gated ion channel that is activated by the neurotransmitter glutamate, the primary excitatory neurotransmitter in the brain. When glutamate binds to the AMPA receptor, it causes the channel to open, allowing positively charged ions to flow into the neuron. This influx of ions triggers an action potential, which is the electrical signal that neurons use to communicate with each other.

Clinical significance[edit | edit source]

Mutations in the GRIA1 gene have been associated with a variety of neurological and psychiatric disorders, including schizophrenia, bipolar disorder, and major depressive disorder. These disorders are thought to be caused, at least in part, by abnormalities in glutamate signaling.

In addition, research has shown that changes in the expression or function of the GRIA1 gene can affect learning and memory. For example, mice that lack the GRIA1 gene show deficits in a type of learning called spatial learning, which involves remembering the location of objects in the environment.

See also[edit | edit source]

References[edit | edit source]



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Contributors: Prab R. Tumpati, MD