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. Author manuscript; available in PMC: 2007 Dec 1.
Published in final edited form as: Neuroscience. 2006 Oct 23;143(2):351–375. doi: 10.1016/j.neuroscience.2006.09.019

Table 2.

Summary of the main ultrastructural features of the subcellular and subsynaptic localization of mGluR subtypes in the basal ganglia, as revealed by high resolution pre-embedding immunogold procedures.

Structure Presynaptic Postsynaptic References
Intracellular     Membrane-bound
Extrasynaptic Perisynaptic Synaptic

Striatum 1a (Thal, Ctx) 1a 1a 1a (Glu) 1a (GABA) 1a, 5: Paquet and Smith, 2003
3 (Ctx) 5 5 5 (Glu, DA) 5 (GABA) 3: Tamaru et al., 2001
4 (Glu, GABA) 4: Corti et al., 2002

GP 4 (GABA) 5 1a 1a (Glu) 1a (GABA) 1a, 5: Hanson and Smith, 1999
5 5 (Glu) 5 (GABA) 4: Corti et al., 2002

STN - 1a 1a 1a (Glu, GABA) - 1a, 5: Kuwajima et al., 2004b
5 5 5 (Glu, GABA)

SNr 4 (Glu, GABA) 5 1a 1a (Glu) 1a (GABA) 1a, 5: Hubert et al., 2001
5 5 (Glu) 5 (GABA) 4: Corti et al., 2002

Source(s) of afferents and chemical phenotype of synapses are indicated in parentheses. Ctx– cortex; DA – dopamine; GABA – γ-aminobutyric acid; Glu – glutamate; Thal – thalamus.

In all basal ganglia, most of the plasma membrane-bound group I mGluRs is extrasynaptic.

No published data is available on the immunogold localization of mGluRs 2, 7, and 8 in all basal ganglia