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M A Ruggero

Publications and source records attributed to M A Ruggero.

29 records · Page 2Linked to original sources
PubMed1986

Basilar membrane mechanics at the base of the chinchilla cochlea. I. Input-output functions, tuning curves, and response phases.

Basilar membrane (BM) velocity was measured at a site 3.5 mm from the basal end of the chinchilla cochlea using the Mössbauer technique. The threshold of the compound action potential recorded at the round window in response to tone bursts was used as an indicator of the physiological state of the cochlea. The BM input-output functions display a compressive nonlinearity for frequencies around the characteristic frequency (CF, 8 to 8.75 kHz), but are linear for frequencies below 7 and above 10.5 kHz. In preparations with little surgical damage, isovelocity tuning curves at 0.1 mm/s are sharply tuned, have Q10's of about 6, minima as low as 13 dB SPL, tip-to-tail ratios (at 1 kHz) of 56 to 76 dB, and high-frequency slopes of about 300 dB/oct. These mechanical responses are as sharply tuned as frequency-threshold curves of chinchilla auditory nerve fibers with corresponding CF. There is a progressive loss of sensitivity of the mechanical response with time for the frequencies around CF, but not for frequencies on the tail of the tuning curve. In some experiments the nonlinearity was maintained for several hours, in spite of a considerable loss of sensitivity of the BM response. High-frequency plateaus were observed in both isovelocity tuning curves and phase-frequency curves.

Action Potentials↗
PubMed1986

Basilar membrane mechanics at the base of the chinchilla cochlea. II. Responses to low-frequency tones and relationship to microphonics and spike initiation in the VIII nerve.

Low-frequency stimuli (40- to 1000-Hz tones) have been used to correlate the motion of the 8-to 9-kHz place of the chinchilla basilar membrane with the cochlear microphonics recorded at the round window and with the responses of auditory nerve fibers with appropriate characteristic frequency. At the lowest stimulus frequencies, maximum displacement of the basilar membrane toward scala tympani occurs in near synchrony with maximum rarefaction at the eardrum and maximum negativity at the round window; at higher frequencies, the mechanical and microphonic response phases progressively lag rarefaction, reaching - 240 deg at 1000 Hz. At most frequencies (40-1000 Hz) near-threshold neural responses, once corrected for neural travel-time and synaptic delays, somewhat lead (by some 40 deg) maximal scala tympani displacement and maximal negativity of the round window microphonics. The variation of sensitivity with frequency is similar for basilar membrane displacement and microphonic responses: Under open-bulla conditions, sensitivity is constant for frequencies between 100 and 1000 Hz; below 100 Hz, sensitivity decreases at rates close to 12 dB/oct toward lower frequencies. Neural response sensitivity matches BM displacement more closely than BM velocity.

Action Potentials↗
PubMed1984

Spontaneous otoacoustic emissions in a dog.

Intense (up to 59 dB SPL) spontaneous otoacoustic emissions are produced by both ears of a young dog. The right ear produces a single, very narrow-band (less than 4 Hz) emission at about 9100 Hz. Brainstem evoked-response audiometry suggests that this emission is generated near the transition between normal and abnormal regions of the cochlea.

Animals↗
PubMed1983

Spontaneous and impulsively evoked otoacoustic emissions: indicators of cochlear pathology?

The first author's right ear produces a spontaneous otoacoustic emission (SOAE) at 7529 Hz and 16 dB SPL. An external continuous tone is able to suppress the SOAE. The 3 dB iso-suppression curve is broadly tuned and displaced, relative to the SOAE, toward higher frequencies. An audiogram notch exists at frequencies just below that of the SOAE. We explain the occurrence of both spontaneous and impulsively evoked OAEs in terms of disruption of active feedback mechanisms of the OHCs upon basilar membrane vibration. According to this hypothesis, each segment of the organ of Corti feeds back positively upon its segment of basilar membrane and negatively upon adjacent segments. If a patch of OHC loss exists, adjacent segments of the basilar membrane are released from the negative feedback and respond to an impulsive stimulus with exaggerated oscillations at their resonance frequencies, thus producing OAEs. At particularly sharp transitions between normal and abnormal regions of the organ of Corti SOAEs may be generated.

Audiometry↗
PubMed1983

Chinchilla auditory-nerve responses to low-frequency tones.

Single unit activity was recorded in the auditory nerves of chinchillas. Period histograms were constructed for responses to tones with frequencies 30-1000 Hz. For low-frequency tones at near-threshold levels, peak period histogram phases for low- and medium-best-frequency (BF) neurons (less than or equal to kHz) ranged from synchronous with condensation at the eardrum to 90 degrees leading it. At near-threshold (but high absolute) levels, high-BF (greater than or equal to 8 kHz) neurons responded in phase with rarefaction. At even higher levels, period histograms for responses of high-BF neurons tended to become bimodal, with one of the modes lagging rarefaction by 90 degrees. Using cochlear microphonics as an indicator of basilar membrane (BM) displacement, at threshold levels, response phase of low- and medium-BF neurons fall within a range between displacement and velocity of the BM toward scala vestibuli. High-BF neurons respond, at threshold (but high) intensities, in phase with BM displacement toward scala tympani. The rates of growth of frequency sensitivity in responses of low-BF (+ 18 dB/oct) and high-BF (+ 12 dB/oct) neurons are consistent with preferred response phases corresponding to BM SV velocity and ST displacement, respectively. At supra-threshold levels high-BF neurons may fire preferentially to both scala tympani displacement and scala vestibuli velocity. These results support the notion that, for high-intensity, low-frequency stimuli, OHC hyperpolarization can induce excitation of the dendrites innervating IHCs.

Animals↗
PubMed1982

Type II cochlear ganglion cells in the chinchilla.

In order to ascertain whether Type II cochlear ganglion cells project to the brain, we have studied the retrograde transport of horseradish peroxidase (HRP) from the cochlear nucleus to the spiral ganglion of the chinchilla. In this animal there exist two types of ganglion neurons, which closely correspond to those previously described in guinea pigs, cats and rats. As in the guinea pig, the majority population (Type I) consists of relatively large, myelinated neurons. The minority population (Type II, 10% of the total population) consists of small, mostly unmyelinated cells, with filamentous cytoplasm and finely grained nuclear chromatin. Type II neurons tend to be clustered toward the peripheral side of Rosenthal's canal, often in close proximity to the intraganglionic spiral bundle. By 24 h after injections of HRP into the cochlear nucleus, incubation of the cochlear ganglion in diaminobenzidine/H2O2 reveals abundant HRP label in both Type I and Type II neurons. Type II neurons, however, tend to be labelled less intensely than Type I neurons. Control experiments, consisting of spillage of HRP solution over the cochlear nucleus, were carried out to determine how much HRP might be picked up by neurons after HRP diffusion. Comparison of cochleae from injected animals and from the control animals suggests that most of the label that was found in ganglion neurons after cochlear nucleus injections represents axonally transported HRP. We conclude, at least tentatively, that Type II neurons project to the brain. The fact that less label is found in Type II neurons that in Type I neurons suggests that the former have thinner axons and/or finer terminals in the cochlear nucleus.

Animals↗
PubMed1982

Kanamycin and bumetanide ototoxicity: anatomical, physiological and behavioral correlates.

Severe hair-cell degeneration and cochlear dysfunction was observed in chinchillas examined at 60 days (or longer) after administration of a single injection of 150 mg/kg kanamycin, followed 2 h later by a single injection of 20 mg/kg bumetanide. Outer hair cells in the cochlear base were most severely affected. While inner and outer hair-cell loss was common, some animals showed large regions along the basilar membrane where almost all inner hair cells were present and almost all outer hair cells were absent. Wherever areas of complete degeneration of the organ of Corti occurred, a small, diffuse population of nerve fibers within the spiral lamina was always present. Single-unit tuning curves correlated best with anatomical observations, compared with the other functional measures of auditory sensitivity that were obtained (behavioral audiogram and compound action potential thresholds). Results indicated that behavioral detection of auditory stimuli is relatively independent of innervation density as long as a few inner hair cells are present. Thus, the cross-fiber threshold envelope of the single-unit tuning curves appeared very similar to the behavioral audiogram.

Animals↗
PubMed1980

Systematic errors in indirect estimates of basilar membrane travel times.

There exist in the literature three attempts to derive basilar membrane travel times from the phase versus frequency characteristics of responses to tones in the auditory nerve [Anderson et al., J. Acoust. Soc. Am. 4., 1131-1139 (1971)], cochlear nucleus [Gibson et al., in Psychophysics and Physiology of Hearing, edited by Evans and Wilson (Academic, New York, 1977), pp. 57-68], and basilar membrane [Robles et al., J. Acoust. Soc. Am. 59, 926-939 (1976)]. It is argued in this paper that these derivations probably have overestimated the actual mechanical travel times. Travel time was originally defined by von Békésy as the latency between the onset of a click stimulus and the onset of basilar membrane vibration. For a linear bandpass system, the frequency-domain equivalent of this latency is the high-frequency asymptotoic slope of the phase lag versus frequency characteristic, which is not generally a linear function. In the neural studies (auditory nerve and cochlear nucleus) it was assumed that the phase versus frequency characteristic was a straight line. Slopes derived under a linear assumption are probably closer to the weighted average group delay (i.e., the center of gravity of the click response) than they are to travel time. In the Mössbauer study of basilar membrane mechanics the latency of the response to clicks was compared with the low-frequency slope of the phase characteristic. The comparison should have been made with the high-frequency slope.

Basilar Membrane↗
PubMed1977

Organization of auditory cortex in the owl monkey (Aotus trivirgatus).

The region of cerebral cortex in the owl monkey that is responsive to acoustic stimulation is located on the dorsal and lateral surfaces of the rostral half of the superior temporal gyrus. Systematic microelectrode mapping of this area has revealed multiple frequency representations. The boundaries of these fields determined electrophysiologically correlate with the architectural boundaries apparent in Nissl stained material. On the basis of combined cytoarchitectonic and electrophysiological maps we have divided auditory cortex into five fields. Two of them, the primary field (AI) and the field rostral to it (R) are somewhat similar architectonically and constitute the central core of auditory cortex. Each of these two fields has a complete and orderly representation of the audible frequency spectrum within it. Surrounding these fields is a belt of cortex in which units are generally less responsive to acoustic stimulation and the frequency organization is more complex than in AI or R. Electrophysiological and cytoarchitectonic evidence suggest that this belt is composed of at least three and possibly four separate auditory fields.

Acoustic Stimulation↗
PubMedDate not supplied

Cochlear delays and traveling waves: comments on 'Experimental look at cochlear mechanics'.

In a recent publication [Audiology 1992;31:301-312], A. Dancer argued that direct and indirect measures of basilar membrane motion are more consistent with theories of cochlear resonance than with the traveling-wave theory. The present communication reviews empirical evidence that contradicts Dancer's argument. Such evidence--recordings of mechanical responses of the basilar and Reissner's membranes to sound--strongly supports the existence of displacement waves that propagate on the basilar membrane from the base of the cochlea toward its apex.

Acoustic Stimulation↗