Fig. 4. Effects of lidocaine on biophysical properties of thalamocortical relay neurons. (A ) Effects of 100 μM lidocaine on the voltage dependence of activation of the I  hconductance (G  h; ordinate), calculated from the amplitudes of I  hpeak tail currents evoked by a repolarization to −78 mV. Tail current amplitudes were normalized to the maximum current levels obtained after the most negative prepulse (−128 mV) and plotted as a function of step potential (E ). Lidocaine decreased the slope factor but had no significant effect on the half-maximal activation potential (details, see Results, third paragraph); * = P < 0.05 (Student t  test). Effects of lidocaine on the kinetics of I  hactivation (B ) and deactivation (C ). (B ) Fast-time constants (τ) of activation plotted as a function of test voltages (E ) in control and in the presence of 100 μM lidocaine. (C ) Representative I  htail current (I ) relaxations upon repolarization to −78 mV after a hyperpolarization to −128 mV in control and in the presence of 100 μM lidocaine. All recordings were performed in the presence of 0.1 mM BaCl2.

Fig. 4. Effects of lidocaine on biophysical properties of thalamocortical relay neurons. (A ) Effects of 100 μM lidocaine on the voltage dependence of activation of the I  hconductance (G  h; ordinate), calculated from the amplitudes of I  hpeak tail currents evoked by a repolarization to −78 mV. Tail current amplitudes were normalized to the maximum current levels obtained after the most negative prepulse (−128 mV) and plotted as a function of step potential (E ). Lidocaine decreased the slope factor but had no significant effect on the half-maximal activation potential (details, see Results, third paragraph); * = P < 0.05 (Student t  test). Effects of lidocaine on the kinetics of I  hactivation (B ) and deactivation (C ). (B ) Fast-time constants (τ) of activation plotted as a function of test voltages (E ) in control and in the presence of 100 μM lidocaine. (C ) Representative I  htail current (I ) relaxations upon repolarization to −78 mV after a hyperpolarization to −128 mV in control and in the presence of 100 μM lidocaine. All recordings were performed in the presence of 0.1 mM BaCl2.

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