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J Neurophysiol (December 1, 2002). 10.1152/jn.00771.2001
Submitted on 17 September 2001
Accepted on 28 June 2002
Departments of 1Neurobiology, Pharmacology, and Physiology and of 2Otolaryngology-Head and Neck Surgery, University of Chicago, Chicago, Illinois 60637
Goldberg, Jay M. and
Alan M. Brichta.
Functional Analysis of Whole Cell Currents From Hair Cells of the
Turtle Posterior Crista. J. Neurophysiol. 88: 3279-3292, 2002. Controlled currents were used to study
possible functions of voltage-sensitive, outwardly rectifying
conductances. Results were interpreted with linearized Hodgkin-Huxley
theory. Because of their more hyperpolarized resting potentials and
lower impedances, type I hair cells require larger currents to be
depolarized to a given voltage than do type II hair cells. "Fast"
type II cells, so-called because of the fast activation of their
outward currents, show slightly underdamped responses to current steps
with resonant (best) frequencies of 40-85 Hz, well above the bandwidth
of natural head movements. Reflecting their slower activation kinetics,
type I and "slow" type II cells have best frequencies of 15-30 Hz
and are poorly tuned, being critically damped or overdamped. Linearized theory identified the factors responsible for tuning quality. Our fast
type II hair cells show only modestly underdamped responses because
their steady-state I-V curves are not particularly steep. The even poorer tuning of our type I and slow type II cells can be
attributed to their slow activation kinetics and large conductances. To
study how ionic currents shape response dynamics, we superimposed sinusoidal currents of 0.1-100 Hz on a small depolarizing steady current intended to simulate resting conditions in vivo. The steady current resulted in a slow inactivation, most pronounced in fast type
II cells and least pronounced in type I cells. Because of inactivation,
fast type II cells have nearly passive response dynamics with
low-frequency gains of 500-1,000 M
. In contrast, type I and slow
type II cells show active components in the vestibular bandwidth and
low-frequency gains of 20-100 and 100-500 M
, respectively. As
there are no differences in the responses to sinusoidal currents for
fast type II cells from the torus and planum, voltage-sensitive currents are unlikely to be responsible for the large differences in
gains and response dynamics of afferents innervating these two regions
of the peripheral zone. The low impedances and active components of
type I cells may be related to the low gains and modestly phasic
response dynamics of calyx-bearing afferents.
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