A brainstem slice preparation was used to investigate GABA-induced res
ponses in the gustatory region of the nucleus of the solitary tract (N
ST) of the hamster. The baseline activities of 91 cells in the rostral
NST were examined extracellularly; 59 cells were located in the rostr
al central (RC), 21 in the rostral lateral (RL), six in the ventral (V
) and five in the medial (M) subdivision of the NST. Of the 80 cells i
n the gustatory region of the NST (RC and RL subdivisions), applicatio
n of GABA produced dose-dependent inhibition in 55 (69 %), excitation
in 9 (11 %) and no effect in 16 cells (22 %). In contrast, only nine c
ells were responsive to baclofen, a GABA(B) agonist. In all subdivisio
ns of the rostral NST, 57 cells were inhibited by GABA and the respons
es of 48 of these were blocked by the specific GABA(A) antagonist, bic
uculline methiodide (BICM). Application of BICM alone often yielded an
excitatory burst of impulses; this effect was eliminated when synapti
c release was blocked by perfusion with a high magnesium physiological
saline solution (PSS/Mg++). The GABA(A)-responsive cells were distrib
uted predominantly within the RC subdivision, whereas the GABA(B)-resp
onsive neurons were mostly in the RL subdivision of the NST. The influ
ences of GABA on the membrane properties of cells within the gustatory
region (RC and RL subdivisions) of the NST were recorded using conven
tional intracellular (16 cells) or whole-cell patch (17 cells) recordi
ng methods. Intracellular recording revealed that GABA produced hyperp
olarisation of the membrane, decreased the firing frequency, and incre
ased the membrane conductance. In the patch-clamp experiments, the app
lication of GABA evoked both inward and outward currents, and an incre
ase in membrane conductance. The reversal potential produced by GABA w
as close to the Cl- equilibrium potential. The effects of GABA were bl
ocked by BICM. These results suggest that (i) GABA has a strong inhibi
tory influence on rostral NST neurons. which in the majority of cells
is mediated through GABA(A) receptors: and (ii) the gustatory region o
f the NST may contain a tonically active GABAergic network.