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Physiological Reviews, Vol. 81, No. 3, July 2001, pp. 1305-1352
Copyright ©2001 by the American Physiological Society
Instituto de Ciencias Biomédicas, Facultad de Medicina, Programa Disciplinario de Fisiología y Biofísica, Universidad de Chile, Santiago, Chile; and Institute for Neuroscience and Hugh Knowles Center, Department of Communication Sciences and Disorders, Northwestern University, Evanston, Illinois
Robles, Luis and
Mario A. Ruggero.
Mechanics of the Mammalian Cochlea. Physiol. Rev. 81: 1305-1352, 2001.
In mammals,
environmental sounds stimulate the auditory receptor, the cochlea, via
vibrations of the stapes, the innermost of the middle ear ossicles.
These vibrations produce displacement waves that travel on the
elongated and spirally wound basilar membrane (BM). As they travel,
waves grow in amplitude, reaching a maximum and then dying out. The
location of maximum BM motion is a function of stimulus frequency, with
high-frequency waves being localized to the "base" of the
cochlea (near the stapes) and low-frequency waves approaching the
"apex" of the cochlea. Thus each cochlear site has a characteristic
frequency (CF), to which it responds maximally. BM vibrations produce
motion of hair cell stereocilia, which gates stereociliar transduction
channels leading to the generation of hair cell receptor potentials and the excitation of afferent auditory nerve fibers. At the base of the
cochlea, BM motion exhibits a CF-specific and level-dependent compressive nonlinearity such that responses to low-level, near-CF stimuli are sensitive and sharply frequency-tuned and responses to
intense stimuli are insensitive and poorly tuned. The high sensitivity
and sharp-frequency tuning, as well as compression and other
nonlinearities (two-tone suppression and intermodulation distortion),
are highly labile, indicating the presence in normal cochleae of a
positive feedback from the organ of Corti, the "cochlear amplifier." This mechanism involves forces generated by the outer hair cells and controlled, directly or indirectly, by their
transduction currents. At the apex of the cochlea, nonlinearities
appear to be less prominent than at the base, perhaps implying that the cochlear amplifier plays a lesser role in determining apical mechanical responses to sound. Whether at the base or the apex, the properties of
BM vibration adequately account for most frequency-specific properties of the responses to sound of auditory nerve fibers.
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