The mammalian ear embeds a cellular amplifier that boosts sound-induced hydromechanical waves as they propagate along the cochlea. The operation of this amplifier is not fully understood and is difficult to disentangle experimentally. In the prevailing view, cochlear waves are amplified by the piezo-electric action of the outer hair cells (OHCs), whose cycle-by-cycle elongations and contractions inject power into the local motion of the basilar membrane (BM). Concomitant deformations of the opposing (or “top”) side of the organ of Corti are assumed to play a minor role and are generally neglected. However, analysis of intracochlear motions obtained using optical coherence tomography calls this prevailing view into question. In particular, the analysis suggests that (i) the net local power transfer from the OHCs to the BM is either negative or highly inefficient; and (ii) vibration of the top side of the organ of Corti plays a primary role in traveling-wave amplification. A phenomenological model derived from these observations manifests realistic cochlear responses and suggests that amplification arises almost entirely from OHC-induced deformations of the top side of the organ of Corti. In effect, the model turns classic assumptions about spatial impedance relations and power-flow direction within the sensory epithelium upside down.
Cochlear mechanics tends to be studied using single-location measurements of intracochlear vibrations in response to acoustical stimuli. Such measurements, due to their invasiveness and often the instability of the animal preparation, are difficult to accomplish and, thus, ideally require stimulus paradigms that are time efficient, flexible, and result in high resolution transfer functions. Here, a swept-sine method is adapted for recordings of basilar membrane impulse responses in mice. The frequency of the stimulus was exponentially swept from low to high (upward) or high to low (downward) at varying rates (from slow to fast) and intensities. The cochlear response to the swept-sine was then convolved with the time-reversed stimulus waveform to obtain first and higher order impulse responses. Slow sweeps of either direction produce cochlear first to third order transfer functions equivalent to those measured with pure tones. Fast upward sweeps, on the other hand, generate impulse responses that typically ring longer, as observed in responses obtained using clicks. The ringing of impulse response in mice was of relatively small amplitude and did not affect the magnitude spectra. It is concluded that swept-sine methods offer flexible and time-efficient alternatives to other approaches for recording cochlear impulse responses.
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