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Departments of 1 Otolaryngology and 2 Physiology and Biophysics, The University of Texas Medical Branch, Galveston, Texas 77555-1063
Linopirdine and XE991, selective
blockers of K+ channels belonging to the KCNQ family, were
applied to hair cells isolated from gerbil vestibular system and to
hair cells in slices of pigeon crista. In type II hair cells, both
compounds inhibited a slowly activating, slowly inactivating component
of the macroscopic current recruited at potentials above
60 mV. The
dissociation constants for linopirdine and XE991 block were <5
µM. A similar component of the current was also blocked by 50 µM
capsaicin in gerbil type II hair cells. All three drugs blocked a
current component that showed steady-state inactivation and a
biexponential inactivation with time constants of ~300 ms and 4 s. Linopirdine (10 µM) reduced inward currents through the
low-voltage-activated K+ current in type I hair cells, but
concentrations up to 200 µM had little effect on steady-state outward
K+ current in these cells. These results suggest that KCNQ
channels may be present in amniote vestibular hair cells.
delayed rectifier; potassium channel; pigeon; gerbil
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