The stratum griseum superficiale (SGS) of the superior colliculus contains
a high concentration of the recently described GABA(C) receptor. In a previ
ous study, it was postulated that activation of these receptors on inhibito
ry interneurons functions to disinhibit projection cells that relay visual
information to the thalamus and brainstem. To test this model, we used in v
itro whole-cell patch-clamp methods to measure effects of GABA and muscimol
on EPSCs and IPSCs evoked in rat SGS by electrical optic layer stimulation
. The neurons were filled with biocytin for later morphological characteriz
ation. As expected, bath applications of GABA and muscimol always strongly
depressed evoked PSCs at concentrations of >100 and >1 muM, respectively. H
owever, at lower agonist concentrations, which most likely activate GABAC b
ut not GABAA receptors, effects were not uniform. Evoked responses were sup
pressed by both agonists in 48% of the neurons, whereas the remaining cells
exhibited enhanced responses with increased evoked EPSCs, decreased evoked
IPSCs, or both types of change. Most morphologically identified cells with
suppressed responses (14 of 17 cells) had morphological characteristics of
putative GABAergic interneurons, whereas almost all cells with enhanced re
sponses (8 of 10 cells) had morphological characteristics of projection cel
ls. Finally, all effects of GABA and muscimol at low concentrations were bl
ocked by (1,2,5,6-tetrahydropyridine-4-yl) methylphosphinic acid, a specifi
c GABAC receptor antagonist, but not by the specific GABAA receptor antagon
ist bicuculline. Taken together, these results indicate that in SGS, GABAC
receptors are predominantly expressed by GABAergic neurons and that activat
ion of these receptors leads to disinhibition of SGS projection cells.