Using anterograde transport of WGA-HRP and the experimental degenerati
on method for identification of corticocuneate (CCT) and primary affer
ent (PAT) terminals in conjunction with gamma-amino butyric acid (GABA
) and glutamate immunocytochemistry, this study has demonstrated that
the GABA-immunoreactive (GABA-IR) neurons in the rat cuneate nucleus w
ere post-synaptic to PATs (some of them being glutamate-IR), GABA-IR a
nd GABA-negative terminals. The HRP-labelled CCTs did not make any syn
aptic contacts with GABA-IR neurons but with some GABA-negative dendri
tes. PATs labelled by HRP or showing degenerating features made direct
synaptic contacts with the dendrites of GABA-IR neurons. Beside the a
bove GABA-IR boutons also showed axosomatic and axodendritic synapses
with the GABA-IR neurons. In 'triple labeling' method for GABA, PAT an
d glutamate, it was found that the PATs which were usually glutamate-p
ositive were presynaptic to the dendrites of GABA-IR neurons. Furtherm
ore, some glutamate-IR terminals which were of non-PAT's origin also s
ynapsed with the dendrites and somata of GABA-IR neurons. It is conclu
ded from this study that the major inputs of GABA-IR neurons were from
glutamate immunopositive PATs and glutamate terminals of non-PATs ori
gin; other GABA-IR terminals either intrinsic or extrinsic also contri
buted to the afferent sources of GABA-IR neurons. The CCTs contributed
very little, if any, to this input. It is suggested that the PATs and
glutamate-IR terminals on GABA-IR neurons may be involved in lateral
inhibition for increase of spatial precision. The synaptic contacts be
tween GABA-IR boutons and dendrites or somata of GABA-IR neurons may p
rovide a possible means for disinhibition. (C) 1997 Elsevier Science I
reland Ltd.