Inner hair cell (IHC) responses are recorded from the apical three turns of
the guinea pig cochlea in order to define the relationship between hair ce
ll depolarization and position of the basilar membrane. At low frequencies,
inner hair cell depolarization is generally observed near basilar membrane
velocity to scala vestibuli, reflecting the putative freestanding nature o
f the IHC's stereocilia. While this is consistent with previous IHC results
, independent of location, and with neural responses for fibers with low be
st frequencies, it is inconsistent with single-unit results from the base o
f the cochlea, where response phase is associated with basilar membrane vel
ocity to scala tympani. Results suggest that the temporal disparity between
IHC and neural data from the base of the cochlea may relate to several fac
tors that influence transmembrane voltage in IHCs. First, extracellular vol
tages (Ingvarsson, 1981; Sellick et al., 1982; Russell and Sellick, 1983) c
an potentially affect low- and high-frequency regions differently because e
lectrical interactions are more likely in the base of the cochlea than in t
he apex (Dallos, 1983, 1985). Second, waveform distortion and kinetic prope
rties associated with voltage-dependent ion channels in the IHC's basolater
al membrane can both influence response phase by adding harmonic components
and lagging the receptor potential by as much as 90 deg. Third, the veloci
ty dependence of IHCs in the apex appears to extend to higher frequencies t
han the velocity dependence demonstrated for IHCs in the base of the cochle
a. These features. which influence the timing of discharges in the auditory
nerve, are compared and evaluated. (C) 1999 Acoustical Society; of America
. [S0001-4966(99)01702-6].