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NEUROPHARMACOLOGY
Department of Physiology, Leiden University Medical Center, Leiden, The Netherlands (J.P.B., L.P.v.d.B., G.Th.v.K., D.L.Y., R.J.v.d.B.); and Department of Pathology, Anatomy, and Cell Biology, Jefferson Medical College, Philadelphia, Pennsylvania (M.E.O.)
In this study, we investigated the effects of the local anesthetic
n-butyl-p-aminobenzoate (BAB) on the delayed rectifier
potassium current of cultured dorsal root ganglion (DRG) neurons using the
patch-clamp technique. The majority of the K+ current of small DRG
neurons rapidly activates and slowly inactivates at depolarized voltages. BAB
inhibited the whole-cell K+ current of these neurons with an
IC50 value of 228 µM. Dendrotoxin K (DTXK), a
specific inhibitor of Kv1.1, reduced the DRG K+ current at +20 mV
by 34%, consistent with an important contribution of channels incorporating
the Kv1.1 subunit to the delayed rectifier current. To further investigate the
mechanism of BAB inhibition, we examined its effect on Kv1.1 channels
heterologously expressed in mammalian tsA201 cells. BAB inhibits the Kv1.1
channels with an IC50 value of 238 µM, similar to what was
observed for the native DRG current. BAB accelerates the opening and closing
of Kv1.1, but does not alter the midpoint of steady-state activation. BAB
seems to inhibit Kv1.1 by stabilizing closed conformations of the channel.
Coexpression with the Kv
1 subunit induces rapid inactivation and reduces
the BAB sensitivity of Kv1.1. Comparison of the heterologously expressed Kv1.1
and native DRG currents indicates that the Kv
1 subunit does not modulate
the gating of the DTXK-sensitive Kv1.1 channels of DRG neurons.
Inhibition of the delayed rectifier current of these neurons may contribute to
the long-duration anesthesia attained during the epidural administration of
BAB.
Address correspondence to: R. J. Van den Berg, Neurophysiology Division, Leiden University Medical Center, Wassenaarseweg 62, P.O. Box 9604, 2300 RC, Leiden, The Netherlands. E-mail: r.j.van_den_berg{at}lumc.nl
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