Light and electron microscopic immunocytochemistry were employed here to sh
ow the distribution of metabotropic glutamate receptors (mGluRs) mGluR2/3 a
nd mGluR5 in laminae I and II of the dorsal horn, to identify their pre- an
d postsynaptic location, and to test colocalization with gamma-aminobutyric
acid (GABA). mGluR2/3 was mainly in the inner part of lamina II; mGluR5 wa
s mainly in laminae I and II. Electron microscopy showed that bath mGluR2/3
and mGluR5 were in perikarya, dendrites, and vesicle-containing profiles.
Two main morphological types of primary afferent terminals can be distingui
shed in the superficial laminae: C1, likely to be endings of unmyelinated f
ibers, and C2, of small myelinated fibers. Quantitative data show that only
a small fraction of C2s stained for either receptor; more common were immu
nopositive dendrites postsynaptic to these terminals, and most common were
appositions between C2s and mGluR5 immunopositive dendrites. Vesicle-contai
ning profiles were characteristically apposed to primary afferent terminals
, mainly C2s. Immunopositivity for mGluRs, especially mGluR2/3, was present
in vesicle-containing profiles apposed to C2, none to C1, and about half o
f the profiles immunostained for either receptor were also stained for GABA
. The presence of presynaptic and postsynaptic mGluRs in both inhibitory an
d excitatory interneurons may contribute to complex processing of fast and
slow responses to peripheral input in superficial laminae. As selective ago
nists of mGluRs may modulate GABA release, the present demonstration of mGl
uRs in GABAergic terminals of presumed interneurons suggests that facilitat
ory effects may involve a mechanism of disinhibition. (C) 1999 Wiley-Liss,
Inc.