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The Journal of Neurophysiology Vol. 87 No. 4 April 2002, pp. 1738-1748
Copyright ©2002 by the American Physiological Society
Neuroscience Center and Kresge Hearing Laboratories, Louisiana State University, New Orleans, Louisiana 70112
Ricci, Anthony
Differences in Mechano-Transducer Channel Kinetics Underlie
Tonotopic Distribution of Fast Adaptation in Auditory Hair Cells. J. Neurophysiol. 87: 1738-1748, 2002. The first step in
audition is a deflection of the sensory hair bundle that opens
mechanically gated channels, depolarizing the sensory hair cells. Two
mechanism of adaptation of mechano-electric transducer (MET) channels
have been identified in turtle auditory hair cells. The rate of fast
adaptation varies tonotopically and is postulated to underlie a
mechanical tuning mechanism in turtle auditory hair cells. Fast
adaptation is driven by a calcium-dependent feedback process associated
with MET channels. The purpose of this paper is to test the hypothesis
that fast adaptation contributes to MET channel kinetics and that
variations in channel kinetics underlie the tonotopic distribution of
fast adaptation. To test for kinetic differences, the open channel
blocker dihydrostreptomycin (DHS) was used. DHS blocked MET currents
from low-frequency cells (IC50 = 14 ± 2 µM)
more effectively than high-frequency cells (IC50 = 75 ± 5 µM), suggesting differences in MET channel properties. DHS block showed similar calcium sensitivities at both papilla locations. No difference in calcium permeation or block of the transducer channels was observed, indicating that the DHS effect was
not due to differences in the channel pore. Slowing adaptation increased DHS efficacy, and speeding adaptation decreased DHS efficacy,
suggesting that adaptation was influencing DHS block. DHS block of MET
channels slowed adaptation, most likely by reducing the peak
intraciliary calcium concentration achieved, supporting the hypothesis
that the rate of adaptation varies with the calcium load per
stereocilia. Another channel blocker, amiloride showed similar efficacy
for high- and low-frequency cells with an IC50 of 24.2 ± 0.5 µM and a Hill coefficient of 2 but appeared to block high-frequency channels faster than low-frequency channels. To further
explore MET channel differences between papilla locations, stationary
noise analysis was performed. Spectral analysis of the noise gave half
power frequencies of 1,185 ± 148 Hz (n = 6) and
551 ± 145 Hz (n = 5) for high- and low-frequency
cells in 2.8 mM external calcium. The half power frequency showed
similar calcium sensitivity to that of adaptation shifting to 768 ± 205 Hz (n = 4) and 289 ± 63 Hz
(n = 4) for high- and low-frequency cells in 0.25 mM
external calcium. Both the pharmacological data and the noise analysis
data are consistent with the hypothesis that the tonotopic distribution
of fast adaptation is in part due to differences in MET channel
kinetics. An increase in the number of MET channels per stereocilia
(termed summation) and or intrinsic differences in MET channel kinetics
may be the underlying mechanism involved in establishing the gradient.
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