Immunoelectron microscopic study of gamma-aminobutyric acid inputs to identified thalamocortical projection neurons in the anterior thalamus of the rat
B. Wang et al., Immunoelectron microscopic study of gamma-aminobutyric acid inputs to identified thalamocortical projection neurons in the anterior thalamus of the rat, EXP BRAIN R, 126(3), 1999, pp. 369-382
We have carried out a semi-quantitative ultrastructural study to determine
the characteristics and distribution of gamma-aminobutyric acid (GABA)-cont
aining constituents of the anterodorsal (AD) and anteroventral (AV) thalami
c nuclei in adult rats. We used a polyclonal antibody to GABA and a postemb
edding immunogold detection method in animals in which the cortical project
ion neurons of these nuclei had been labelled by retrograde transport of ch
olera toxin/horseradish peroxidase (HRP) injected into the retrosplenial gr
anular cortex. Two types of GABA-immunopositive structures were identified,
with gold particle densities 4-40 times higher than the highest densities
over blood-vessel lumens and areas of empty resin: (1) an apparently homoge
neous population of axon terminals with Gray type-2 (symmetric) synaptic co
ntacts corresponding to F-axon terminals; and (2) small-medium sized myelin
ated axons scattered individually or in small groups within the neuropil wh
ich may be their parent axons. These axons and terminals may originate from
the ipsilateral thalamic reticular nucleus; others may arise from the basa
l forebrain or brainstem. The GABA-immunopositive terminals comprised appro
ximately 16% of all axon terminal profiles in AD and 12% in AV, a significa
nt difference. However, because the immunoreactive axon terminals in AD wer
e significantly larger than those in AV (1.09+/-0.47 mu m(2) vs 0.90+/-0.43
mu m(2)) and would therefore be encountered more frequently, it is not pos
sible to conclude that the GABAergic innervation of AD is heavier than that
of AV. The GABA-positive terminals established synaptic contacts with cell
bodies and dendrites of all sizes (some of which were HRP-labelled) with t
he following frequency distribution (AD/AV, no significant difference): som
ata 5%/7%; large dendrites (greater than or equal to 1.5 mu m) 14%/9%; medi
um dendrites (1.00-1.49 mu m) 35%/45% and small dendrites (<1 mu m) 46%/40%
. Despite evidence from previous studies, we found no evidence in this stud
y for the presence of GABAergic interneurons or for GABA-containing project
ion neurons in AD or AV.