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1Department of Anatomy and Neurobiology, University of Tennessee, Memphis, Tennessee; and 2Departments of Neurology and Physiology and Biophysics, University of Washington, Veterans Administration Puget Sound Health Care System, Seattle Washington
Submitted 1 September 2006; accepted in final form 9 January 2007
Pyramidal neurons from layers II/III of somatosensory and motor cortex express multiple Kv1
-subunits and a current sensitive to block by
-dendrotoxin (
-DTX). We examined functional roles of native Kv1 channels in these cells using current-clamp recordings in brain slices and current- and voltage-clamp recordings in dissociated cells.
-DTX caused a significant negative shift in voltage threshold for action potentials (APs) and reduced rheobase. Correspondingly, a ramp-voltage protocol revealed that the
-DTXsensitive current activated at subthreshold voltages. AP width at threshold increased with successive APs during repetitive firing. The steady-state threshold width for a given firing rate was similar in control and
-DTX, despite an initially broader AP in
-DTX. AP voltage threshold increased similarly during a train of spikes under control conditions and in the presence of
-DTX.
-DTX had no effect on input resistance or resting membrane potential and modest effects on the amplitude or width of a single AP. Accordingly, experiments using AP waveforms (APWs) as voltage protocols revealed that
-DTXsensitive current peaked late during the AP repolarization phase. Application of
-DTX increased the rate of firing to intracellular current injection and increased gain (multiplicative effects), but did not alter spike-frequency adaptation. Consistent with these findings, voltage-clamp experiments revealed that the proportion of outward current sensitive to
-DTX was highest during the interval between two APWs, reflecting slow deactivation kinetics at 50 mV. Finally,
-DTX did not alter the selectivity of pyramidal neurons for DC versus time-varying stimuli.
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