1 The e ects of lignocaine [lidocaine] HCl (0.6 mM ± 1 mM) on the membrane electrical properties and action potential ®ring of neurones of the ventral posterolateral (VPL) nucleus of the thalamus were investigated using whole cell recording techniques in rat brain slices in vitro. 2 Bath application of lignocaine reversibly decreased the input resistance (R i ) of VPL neurones. This e ect was observed at low, clinically sedative and analgesic concentrations (i.e., maximal amplitude at 10 mM) whereas higher concentrations (300 mM ± 1 mM) had no e ect on R i . 3 Lignocaine (10 ± 100 mM) depolarized VPL neurones up to 14 mV in a reversible manner. 4 Consistent with a decreased R i , low concentrations of lignocaine shunted the current required for spike generation in the tonic pattern. Lignocaine increased the threshold amplitude of current required for ®ring and decreased the tonic ®ring frequency, without concomitant elevation of the voltage threshold for ®ring or reduction in the maximal rate of rise (dV/dt max ) of spikes. 5 Low concentrations of lignocaine shunted low threshold spike (LTS) burst ®ring evoked either from hyperpolarized potentials or as rebound bursts on depolarization from prepulse-conditioned potentials. 6 Higher concentrations of lignocaine (300 mM ± 1 mM), not associated with a decrease in R i , elevated the voltage threshold for ®ring and reduced the dV/dt max of spikes in a concentration-dependent fashion. 7 In conclusion, low concentrations of lignocaine shunted tonic and burst ®ring in VPL neurones by decreasing R i , a mechanism not previously described for local anaesthetics in the CNS. We suggest that a decreased resistance in thalamocortical neurones contributes to the sedative, analgesic, and anaesthetic properties of systemic lignocaine in vivo.