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Department of Pharmacology, Emory University School of Medicine, Atlanta, GA 30322
3To whom correspondence should be addressed.
Glutamate is the most widespread excitatory neurotransmitter in the
mammalian brain. Two classes of glutamate receptor have been cloned,
the ionotropic (ligand-gated ion channels) and the metabotropic (G
proteincoupled receptors). Three subclasses of ionotropic glutamate
receptors are known; they are named after selective agonists, i.e.,
-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA),
N-methyl-D-aspartate (NMDA) and kainate
receptors. Fifteen functional subunits assemble together in
heteromultimeric complexes to form these receptors as follows:
GluR1GluR4 for AMPA; GluR5GluR7 and KA1-KA2 for kainate; and NR1,
NR2A-NR2D and NR3 for NMDA receptors. Within a subclass, the subunit
composition strongly influences the pharmacologic and biophysical
properties of the receptors. The metabotropic glutamate receptors fall
into the following three groups, each containing two or more individual
receptor proteins: group I (mGluR1, mGluR5), group II (mGluR2, mGluR3),
and group III (mGluR4, mGluR6, mGluR7 and mGluR8). In contrast to the
ionotropic receptors, the metabotropic glutamate receptors appear to
act as monomers or homodimers rather than heteromers. Messenger RNAs
encoding several ionotropic subunits and a mGluR4-like receptor have
been identified in taste buds. Although controversial, the evidence is
consistent with an NMDA receptor serving as a primary taste transducer
for monosodium glutamate (MSG), and a metabotropic glutamate receptor
modulating the flavor-enhancing effect of MSG. Thus the
neurotransmitter glutamate is intimately involved in the central
processing of taste information.
KEY WORDS: taste receptor
-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid N-methyl-D-aspartate metabotropic sensory transduction