The Journal of the Acoustical Society of America · 2005 · 53 citations · 65 references
Life SciencesNeurobiologyNeuroscienceHearing ScienceSensory NeuroscienceSensory PhysiologyAuditory NeurobiologyAuditory NeurophysiologyAuditory NeuroscienceAuditory PathwaysAuditory PhysiologyCochlear NeuroscienceAmplificationBasilar Membrane ResponseCochlear Amplifier FunctionCochlear BaseCochlear NeurophysiologyCochlear PhysiologyElectrical StimulationOlivocochlear System
Despite the insights obtained from click responses, the effects of medial-olivocochlear (MOC) efferents on click responses from single-auditory-nerve (AN) fibers have not been reported. We recorded responses of cat single AN fibers to randomized click level series with and without electrical stimulation of MOC efferents. MOC stimulation inhibited (1) the whole response at low sound levels, (2) the decaying part of the response at all sound levels, and (3) the first peak of the response at moderate to high sound levels. The first two effects were expected from previous reports using tones and are consistent with a MOC-induced reduction of cochlear amplification. The inhibition of the AN first peak, which was strongest in the apex and middle of the cochlea, was unexpected because the first peak of the classic basilar-membrane (BM) traveling wave receives little or no amplification. In the cochlear base, the click data were ambiguous, but tone data showed particularly short group delays in the tail-frequency region that is strongly inhibited by MOC efferents. Overall, the data support the hypothesis that there is a motion that bends inner-hair-cell stereocilia and can be inhibited by MOC efferents, a motion that is present through most, or all, of the cochlea and for which there is no counterpart in the classic BM traveling wave.
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Evoked Mechanical Responses of Isolated Cochlear Outer Hair Cells
William E. Brownell, Charles R. Bader, Daniel Bertrand et al. · Science · 1985 · 1.8K citations