By using the whole cell patch recording technique in vitro, we examined the
voltage-dependent firing patterns of 69 interneurons in the rat dorsal lat
eral geniculate nucleus (LGN). When held at a hyperpolarized membrane poten
tial, all interneurons responded with a burst of action potentials. In 48 i
nterneurons, larger current pulses produced a bursting oscillation. When re
latively depolarized, some interneurons produced a tonic train of action po
tentials in response to a depolarizing current pulse. However, most interne
urons produced only oscillations, regardless of polarization level. The osc
illation was insensitive to the bath application of a combination of blocke
rs to excitatory and inhibitory synaptic transmission, including 30 mu M 6,
7-dinitroquinoxaline2,3-dione, 100 mu M (+/-)-2-amino-5-phosphonopentanoic
acid, 20 mu M bicuculline, and 2 mM saclofen, suggesting an intrinsic event
. The frequency of the oscillation in interneurons was dependent on the int
ensity of the injection current. Increasing current intensity increased the
oscillation frequency. The maximal frequency of the oscillation was 5-15 H
z for most cells, with some ambiguity caused by the difficulty of precisely
defining a transition from oscillatory to regular firing behavior. In cont
rast, the interneuron oscillation was Little affected by preceding depolari
zing and hyperpolarizing pulses. In addition to being elicited by depolariz
ing current injections, the oscillation could also be initiated by electric
al stimulation of the optic tract when the interneurons were held at a depo
larized membrane potential. This suggests that interneurons may be recruite
d into thalamic oscillations by synaptic inputs. These results indicate tha
t interneurons may play a larger role in thalamic oscillations than was pre
viously thought.