Medial efferent inhibition suppresses basilar membrane responses to near characteristic frequency tones of moderate to high intensities

1997 ◽  
Vol 102 (3) ◽  
pp. 1734-1738 ◽  
Author(s):  
Ian J. Russell ◽  
Euan Murugasu
Author(s):  
Shuangqin Liu ◽  
Douglas A. Gauthier ◽  
Ethan Mandelup ◽  
Robert D. White

In this research, an uncoiled scale gerbil cochlea is designed and fabricated. The cochlea model is an uncoiled, 16 times scale model of the real gerbil cochlea and has only one duct. Both the basilar membrane width and the duct size vary along the length of the device, in analogy to the physiology. The cochlea duct is filled with silicone oil and driven by a modal exciter (shaker) at different frequencies. The movement of the basilar membrane is measured using laser vibrometry at different locations along the basilar membrane. The ratio of the basilar membrane velocity to drive velocity is computed and plotted. The characteristic frequency of the model varies from 7000 Hz at 2 cm from the base of the cochlea to 350 Hz at the 15 cm from the base. Two different viscosities silicone oil, 20 cSt and 500 cSt are used for the basilar membrane movement measurements. A WKB method is applied to the calculation of the basilar membrane movement of the scale cochlea model, in which the fluid motion is fully three dimensional.


2008 ◽  
Vol 100 (5) ◽  
pp. 2899-2906 ◽  
Author(s):  
Andrei N. Temchin ◽  
Nola C. Rich ◽  
Mario A. Ruggero

Spontaneous activity and frequency threshold tuning curves were studied in thousands of auditory nerve fibers in chinchilla. The frequency distribution of spontaneous activity rates is strongly bimodal for auditory nerve fibers with characteristic frequency <3 kHz but only mildly bimodal for the entire sample. Spontaneous activity rates and thresholds at the characteristic frequency are inversely related. Auditory-nerve fibers with low spontaneous rate have tuning curves with lower tip-to-tail ratios and more sharply tuned tips than the tuning curves of fibers with high spontaneous rates. It is shown here that this dependence of tuning on spontaneous rates is consistent with a previously unnoticed nonmonotonic dependence on iso-velocity criterion of the frequency tuning of basilar membrane vibrations.


2005 ◽  
Vol 93 (6) ◽  
pp. 3635-3648 ◽  
Author(s):  
Andrei N. Temchin ◽  
Alberto Recio-Spinoso ◽  
Pim van Dijk ◽  
Mario A. Ruggero

Responses to tones, clicks, and noise were recorded from chinchilla auditory-nerve fibers (ANFs). The responses to noise were analyzed by computing the zeroth-, first-, and second-order Wiener kernels (h0, h1, and h2). The h1s correctly predicted the frequency tuning and phases of responses to tones of ANFs with low characteristic frequency (CF). The h2s correctly predicted the frequency tuning and phases of responses to tones of all ANFs, regardless of CF. Also regardless of CF, the kernels jointly predicted about 77% of the features of ANF responses to “frozen” samples of noise. Near-CF group delays of kernels and signal-front delays of responses to intense rarefaction clicks exceeded by 1 ms the corresponding basilar-membrane delays at both apical and basal sites of the chinchilla cochlea. This result, confirming that synaptic and neural processes amount to 1 ms regardless of CF, permitted drawing a map of basilar-membrane delay as a function of position for the entire length of the chinchilla cochlea, a first for amniotic species.


Author(s):  
R.J. Mount ◽  
R.V. Harrison

The sensory end organ of the ear, the organ of Corti, rests on a thin basilar membrane which lies between the bone of the central modiolus and the bony wall of the cochlea. In vivo, the organ of Corti is protected by the bony wall which totally surrounds it. In order to examine the sensory epithelium by scanning electron microscopy it is necessary to dissect away the protective bone and expose the region of interest (Fig. 1). This leaves the fragile organ of Corti susceptible to physical damage during subsequent handling. In our laboratory cochlear specimens, after dissection, are routinely prepared by the O-T- O-T-O technique, critical point dried and then lightly sputter coated with gold. This processing involves considerable specimen handling including several hours on a rotator during which the organ of Corti is at risk of being physically damaged. The following procedure uses low cost, readily available materials to hold the specimen during processing ,preventing physical damage while allowing an unhindered exchange of fluids.Following fixation, the cochlea is dehydrated to 70% ethanol then dissected under ethanol to prevent air drying. The holder is prepared by punching a hole in the flexible snap cap of a Wheaton vial with a paper hole punch. A small amount of two component epoxy putty is well mixed then pushed through the hole in the cap. The putty on the inner cap is formed into a “cup” to hold the specimen (Fig. 2), the putty on the outside is smoothed into a “button” to give good attachment even when the cap is flexed during handling (Fig. 3). The cap is submerged in the 70% ethanol, the bone at the base of the cochlea is seated into the cup and the sides of the cup squeezed with forceps to grip it (Fig.4). Several types of epoxy putty have been tried, most are either soluble in ethanol to some degree or do not set in ethanol. The only putty we find successful is “DUROtm MASTERMENDtm Epoxy Extra Strength Ribbon” (Loctite Corp., Cleveland, Ohio), this is a blue and yellow ribbon which is kneaded to form a green putty, it is available at many hardware stores.


1968 ◽  
Vol 11 (1) ◽  
pp. 63-76
Author(s):  
Donald C. Teas ◽  
Gretchen B. Henry

The distributions of instantaneous voltage amplitudes in the cochlear microphonic response recorded from a small segment along the basilar membrane are described by computing amplitude histograms. Comparisons are made between the distributions for noise and for those after the addition to the noise of successively stronger sinusoids. The amplitudes of the cochlear microphonic response to 5000 Hz low-pass noise are normally distributed in both Turn I and Turn III of the guinea pig’s cochlea. The spectral composition of the microphonic from Turn I and from Turn III resembles the output of band-pass filters set at about 4000 Hz, and about 500 Hz, respectively. The normal distribution of cochlear microphonic amplitudes for noise is systematically altered by increasing the strength of the added sinusoid. A decrease of three percent in the number of small amplitude events (±1 standard deviation) in the cochlear microphonic from Turn III is seen when the rms voltage of a 500 Hz sinusoid is at −18 dB re the rms voltage of the noise (at the earphone). When the rms of the sinusoid and noise are equal, the decrease in small voltages is about 25%, but there is also an increase in the number of large voltage amplitudes. Histograms were also computed for the output of an electronic filter with a pass-band similar to Turn III of the cochlea. Strong 500 Hz sinusoids showed a greater proportion of large amplitudes in the filter output than in CM III . The data are interpreted in terms of an anatomical substrate.


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