Pentobarbital Depressant Effects Are Independent of GABA Receptors in Auditory Thalamic Neurons

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Abstract
Pentobarbital, a general anesthetic, has received extensive study for its ability to potentiate inhibition at GABAAsubtype of receptors for GABA. Using whole cell current-clamp techniques and bath applications, we determined the effects of pentobarbital and GABA receptor antagonists on the membrane properties and tonic or burst firing of medial geniculate neurons in thalamic slices. Pentobarbital (0.01–200 μM) induced depressant effects in 50 of 66 neurons (76%). Pentobarbital hyperpolarized neurons by a mean of 3 mV and decreased the number of action potentials in tonic firing, evoked by current pulse injection from near the resting potential. Pentobarbital also decreased burst firing or low threshold Ca2+-spikes, evoked by current pulse injection into neurons at potentials hyperpolarized from rest. The blockade of tonic and burst firing, as well as low threshold Ca2+-spikes, was surmountable by increasing the amplitude of input current. The GABAAreceptor antagonists, bicuculline (100 μM) and picrotoxinin (50–100 μM), did not block the depressant effects of pentobarbital (10 μM). The GABABreceptor antagonist, saclofen (200 μM), and GABACreceptor antagonist, (1,2,3,6-tetrahydropyridine-4-yl)methylphosphinate (10–50 μM), did not significantly alter the depressant effects. Pentobarbital produced excitatory effects (0.1–50 μM) on 11 neurons (17%) but had no effects on 5 neurons (7%). The excitation consisted of approximately 3 mV depolarization, increased tonic and burst firing and the rate of rise and amplitude of low threshold Ca2+spikes. These effects were associated with a increase in input resistance. In contrast, the depressant effects of pentobarbital correlated to a decreased input resistance measured with hyperpolarizing current pulse injection (IC50= 7.8 μM). Pentobarbital reduced Na+-dependent rectification on depolarization and lowered the slope resistance over a wide voltage range. Tetrodotoxin eliminated both Na+-dependent rectification and the pentobarbital-induced decrease in membrane resistance at depolarized voltages in two-thirds of the neurons. The pentobarbital-induced decrease in membrane resistance at voltages hyperpolarized from rest was not evident during co-application with Cs+, known to block the hyperpolarization-activated rectifiers. In summary, the pentobarbital acted at low concentrations to depress thalamocortical neurons. The depression resulted from decreased rectification on depolarization, which no longer boosted potentials over threshold, and an increased conductance that shunted spike generation. The depressant effects of pentobarbital did not involve known types of GABA receptor interactions.