SYNAPTIC ORGANIZATION OF PULVINAR PROJECTING PORTIONS OF THE CAT THALAMIC RETICULAR NUCLEUS.

J.W.Boss; Z.B.Baldauf; M.E.Bickford*

Anatom. Sci. and NeuroBiol., Univ. of Louisville, Louisville, KY, USA

Intrinsic connections between GABAergic cells in the thalamic reticular nucleus (TRN) may play an important role in synchronizing the activity of the TRN and its target nuclei in the dorsal thalamus. We recently examined the synaptic circuitry of the cat perigeniculate nucleus (PGN), which projects specifically to the dorsal lateral geniculate nucleus (dLGN), and were surprised to find very few GABAergic contacts on PGN cells. To determine whether this reflects the general organization of the visual sector of the TRN, or is a unique feature of the PGN, we have begun to examine the synaptic organization of portions of the TRN that project to the cat pulvinar nucleus. We injected tracers into the pulvinar nucleus to label pulvinar-projecting TRN cells (PP-TRN). We then characterized the synaptic contacts on PP-TRN cells labeled by retrograde transport in tissue stained for GABA using postembedding immunocytochemistry. In contrast to our previous study, where GABAergic contacts made up as little as 3% of the input to PGN cells, we found that PP-TRN cells received up to 42% of their input from GABAergic terminals. Most of these profiles contained densely packed synaptic vesicles characteristic of axon terminals, although occasional GABAergic dendrodendritic contacts were also observed. Most other contacts in the PP-TRN were made by small non-GABAergic profiles (42%, presumed corticothalamic terminals). In contrast to the PGN, where contacts made by large non-GABAergic terminals (presumed thalamocortical collaterals) provide the majority of the input to PGN cells, large non-GABAergic profiles were not observed in the PP-TRN. These results suggest that connections between GABAergic cells are more common in the main body of the TRN than in the PGN, and thalamocortical collateral projections may be more prevalent in the PGN, or may display distinct morphologies in the PGN and TRN.
Support Contributed By: NIH NS35377