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. Author manuscript; available in PMC: 2010 Jul 15.
Published in final edited form as: Annu Rev Pharmacol Toxicol. 2010;50:295–322. doi: 10.1146/annurev.pharmtox.011008.145533

Table 1.

Key features of mGluRs

Group Receptor/splice
variants
CNS expression Synaptic localization Signaling pathways of group

Group I mGluR1
a,b,c,d,e,f
Taste mGluR1
Widespread in neurons
Taste buds
Predominantly
 postsynaptic
Phospholipase C stimulation
Stimulation of adenylyl cyclase
(some systems)
MAP kinase phosphorylation

mGluR5
a,b
Widespread in neurons,
 astrocytes

Group II mGluR2 Widespread in neurons Presynaptic and
 postynaptic
Inhibition of adenylyl cylcase
Activation of K+ channels
Inhibition of Ca++ channels

mGluR3
GRM3A2
GRM3A4
GRM3A2A3
Widespread in neurons,
 astrocytes

Group III mGluR4 Widespread in neurons,
 High in cerebellum
Predominantly
 presynaptic
Inhibition of adenylyl cylcase
Activation of K+ channels
Inhibition of Ca++ channels
Taste mGluR4
Taste buds

mGluR6
a,b,c
Retina Postsynaptic in
 ON-bipolar retinal cells
Stimulation of cGMP
 phosphodiesterase (mGluR6)

mGluR7
a,b,c,d,e
Widespread in neurons Active zone of presynaptic
 terminals

mGluR8
a,b,c
Lower and more restricted
 expression than
 mGluR4/7
Predominantly
 presynaptic