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Registration of spontaneous cochlear emissions by means of Fourier transformation.

Fourier transformation is a suitable procedure for the detection of spontaneous cochlear emissions. In the setup used, the microphone lies unsupported at the entrance to the external auditory canal; after amplification and optional filtering, the signal is processed digitally. The frequency distribution of the emissions is considerably narrow and shows alterations in frequency and intensity. Emissions seem to occur in slightly damaged cochleas.

Adolescent

Influence of thyroid state and improved hypoxia tolerance on noise-induced cochlea damage.

Guinea pigs were exposed to pure tone noise (2.7 kHz, 130 dB, 1 h) and cochlear microphonic potentials were measured 24 h after exposure. There is the possibility to modify the resulting noise-induced cochlea damage by regulating the function of the thyroid gland to alter the rate of metabolism. A hypofunction of the thyroid gland during sound exposure lessens, an over-function aggravates the damage. After gradual adaptation of the animals to a simulated 10,000 m altitude, the electrophysiologically demonstratable noise-induced damage was reduced. This might be explained by the greater hypoxia tolerance and perhaps additional better oxygen supply to the receptor cells.

Altitude

Effects of modern loop diuretics on the inner ear a quantitative evaluation using computer technics.

The effects of some modern high ceiling loop diuretics on the guinea-pig's inner ear are tested. Short-time experiments are run registrating the cochlear microphonic potentials (CMP) before and after i.v. bolus injections of a diuretic. A 100-point matrix program is performed by automatic sampling of the CMPs after stimulating by five frequencies at 20 sound pressure levels each. Data can be plotted in different scales within 10 min after the end of a whole-day experiment. The data are on-line processed by a IBM 1800 computer.

Animals

[Influence of thyroid state on noise-induced cochlea damage (author's transl)].

Guinea pigs were exposed to pure tone noise (2.7 kHz, 130 dB, 1 h) and cochlear microphonic potentials were measured after 5 days. It is possible, to modify the resulting damage by experimentally altering the rate of metabolism by regulating the function of the thyroid gland. (table: see text) A hypofunction of the thyroid gland during sound exposure lessens, an over-function aggravates the damage. This effect possibly results from the influence on the metabolism exerted by the adenylic system. This conclusion leads to new viewpoints concerning prophylaxis, therapy and metaphylaxis in cases of noise deafness.

Adenylyl Cyclases

Suppression of the auditory frequency following response during visual attention.

Frequency-following responses (FFRs) were recorded from unanesthetized cats with electrodes chronically implanted in the cochlear nucleus and on the round window. Tone bursts of different frequencies (irrelevant stimuli) were presented repetitively (85 dB SPL, 1/sec) as background before, during, and after the presentation of a visual discrimination task (relevant stimuli) which attempted to alter the attentive state of the animals. The mean peak-to-peak amplitudes of the FFRs from the cochlear nucleus were significantly reduced in amplitude during attention to the visual discrimination stimuli when compared with the amplitudes of the pretest- and posttest-control periods. However, at the round window (cochlear microphonic) no significant differences in amplitude were observed for the same periods. Although the amplitudes of the FFRs were reduced in amplitude at all frequencies during visual attention, much greater suppression occurred at the middle frequencies (700-2000 Hz) than at higher or lower frequencies. These data suggest that during visual attention the FFRs are attenuated by a central inhibitory mechanism.

Animals

A reproducible technique for breaking glass micropipettes over a wide range of tip diameters.

A new simple technique for the accurate modification of microelectrode and micropipette tips by breaking has been developed. The breaking is done by longitudinally inserting a micropipette into a larger previously broken pipette for stability and by applying a force on the micropipette to cause it to break. Tips will break cleanly at an easily predetermined diameter over a range of 3-200 micrometers.

Animals

Frequency selectivity in the auditory periphery: similarities between damaged and developing ears.

Single fiber tuning curves (stimulus frequency versus neural threshold curves) were obtained from 198 auditory nerve fibers in 24 kittens between birth and the 16th postnatal day and from 74 auditory nerve fibers in adult cats. Three developmental stages during which adult-like frequency-resolving capacity was acquired were identified. During the early stage of postnatal development, all auditory nerve fibers were essentially untuned and responded to a narrow range of low to middle frequency tone bursts presented at intensities exceeding 110 dB sound pressure level (SPL) re 20 muPa. In the intermediate stage, which occurred during the second postnatal week, auditory nerve fibers tuned to low- and mid-range frequencies acquired adult-like frequency-resolving capacity. Fibers tuned to high frequencies, which were recorded later in development than those tuned to lower frequencies, were as sharply tuned as their adult counterparts, but exhibited a low contrast between thresholds at characteristic frequency (tip) and lower (tail) frequencies (ie, low tip-to-tail ratios). Adult-like tuning curves were observed during the third stage, primarily as a consequence of the acquisition of adult-like tip-to-tail ratios. Our understanding of the cochlear mechanism(s) by which frequency selectivity is produced in adult animals has recently been enhanced by a combined anatomy and physiology investigation conducted by Liberman and Dodds, in which clear anatomic foci of cochlear damage were identified in cats with functionally characterized hearing loss. Similarly, descriptions of anatomic differentiation in the feline auditory end-organ correlate with functional measures of peripheral auditory system development. In this report, anatomic and physiologic similarities between developing and damaged ears are considered in an attempt to better characterized the process whereby normal frequency selectivities and thresholds are developed. Our findings support the notion that anatomic changes in the cochlea during development, primarily the development of adult-like anatomic relations between the tectorial membrane and sensory cells, underlie the acquisition of adult-like auditory nerve fiber tuning.

Age Factors

Efferent neural control of cochlear mechanics? Olivocochlear bundle stimulation affects cochlear biomechanical nonlinearity.

We confirm the report of Mountain (Mountain, D.C. (1980): Science 210, 77-72) that stimulating the crossed olivocochlear bundle (COCB) can change the magnitude of the distortion product (f2-f1) in the ear-canal sound pressure. Our results are extended to include (2f1-f2) as well as (f2-f1) from anesthetized chinchillas with both middle-ear muscles sectioned. In contrast to Mountain's report, the polarity of the change can be either positive, negative or absent, depending on the choice of two-tone stimulus frequencies. The influence of two-tone stimulus level is also complex, but we have not yet seen the polarity of the COCB effect change with stimulus level. The magnitude and polarity of the change in (2f1-f2) are not simply related to those for (f2-f1). The effect of COCB stimulation is abolished when scala tympani is perfused with artificial perilymph containing 10(-5) M d-tubocurarine. These results demonstrate that the COCB effect is postsynaptic, probably mediated by outer hair cells. We suggest that the normal cochlea contains an active biomechanical mechanism which reduces the damping of the cochlear-partition motion and is modulated by activating the efferents. It is thus possible that the central nervous system may be able to control the dynamics of the motion of the cochlear partition.

Acoustic Stimulation

Spontaneous, click-, and toneburst-evoked otoacoustic emissions from normal ears.

Evoked and spontaneous otoacoustic emissions were recorded bilaterally in a group of normal subjects (n = 14) using clicks and tonebursts at four frequencies (0.5, 1, 1.5, and 3 kHz). All ears (n = 28) demonstrated evoked emissions, but not to every stimulus type. The 0.5-kHz toneburst evoked emissions in only 10 (36%) ears, the 1.5-kHz toneburst in all ears, and the remaining stimuli in at least 80% of ears. Two distinct patterns of evoked emissions were identified. Five (18%) ears showed short, broadband click-evoked emissions lasting less than 20 ms after stimulus onset. In these ears, toneburst-evoked emissions were often more prominent than click-evoked emissions and no spontaneous emissions were detected. Twenty-three (82%) ears showed click-evoked emissions lasting longer than 20 ms poststimulus onset. Spectral analysis of these emissions demonstrated several (2-10) narrow frequency peaks. Highly similar peaks were present in the spectra of toneburst-evoked emissions within the range of toneburst spectra. Spontaneous emissions were recorded in 12 of the 23 ears. In these ears, at the frequencies of spontaneous emissions, prominent peaks in both click- and toneburst-evoked emission spectra were always present. Otoacoustic emission characteristics correlated significantly between the ears of individual subjects inferring that a symmetrical cochlear mechanism generates otoacoustic emissions.

Acoustic Stimulation

Mutant golden hamsters with an abnormal outer hair cell stereociliary arrangement.

A new malformation of the inner ear was found in golden hamster reared at our institute. It was studied using electron microscope and auditory electrophysiological measurements including auditory brainstem response (ABR), whole nerve action potential (AP) cochlear microphonic (CM) potential, and the summating potential (SP). The stereocilia on individual first row of outer hair cells in the hamsters with malformed inner ears (F-K hamsters) were arranged in a triple W form, but the entire bundle of stereocilia was irregular in orientation. These anomalies were seen in approximately 70 to 85% of sensory hairs, in all rotations, with no difference between the right and left sides. The cuticles of the first row of outer hair cells were displaced, but lower portions did not appear to be affected. ABR and SP revealed no differences from normal hamsters and it is believed that the F-K hamsters' hearing ability was normal. The CM potential and the amplitude of AP in the F-K hamsters were significantly lower, at 50 to 80 dB sound pressure level (SPL). The linear portions of the CM input-output relation curve were separated by 4 to 6 dBSPL and the saturating voltage levels differed by 2.5 to 3.0 microV. Based on these results, the actually-measured CM potentials were shown to represent a summation of the reaction of the three individual rows of outer hair cells.

Action Potentials

Evoked otoacoustic emissions in guinea pig: basic characteristics.

Different types of evoked otoacoustic emissions (EOAEs) such as stimulus frequency emissions, tone burst and click EOAEs, were investigated in the guinea pig. Their correlates on cochlear microphonic potential were also recorded. Although it was confirmed that click EOAEs are difficult to detect in the guinea pig, partly because their delay (2 to 3 ms, measured on tone burst EOAEs) is much shorter than in man, other types of OAE were found in the interval (1.5-5 kHz) for almost every normal animal. Many of their properties were quite different from man, for instance their small number, low level, and the wide frequency range of some of them (up to 500 Hz), suggesting that they represent a sort of continuum. It is proposed that these particularities may not arise from different generating mechanisms but should be correlated with the well-known differences in hair cells patterns.

Acoustic Stimulation

[Evoked otoacoustic emissions and their modification by contralateral acoustic stimulation].

The active vibration of the basilar membrane as well as evoked otoacoustic emissions (EOAE) are probably based on the motile properties of cochlear outer hair cells (OHC). In the present study we examined the effects of contralateral acoustic stimulation on ipsilateral EOAE and thereby the active cochlear micromechanics. Contralateral white noise with intensities below 30 dB HL enhanced the EOAE amplitude, whereas higher sound levels reduced the evoked acoustic emissions. Similar effects of contralateral acoustic stimuli on ipsilateral EOAE were observed in patients with a conductive hearing loss. However, the required sound levels were higher compared to probands with normal hearing. In controls with unilateral deaf patients white noise up to 60 dB HL did not alter the EOAE amplitude. We concluded, that in patients with normal hearing or unilateral conductive hearing loss, effects of contralateral acoustic stimulation on evoked ipsilateral sound emissions may be due to the activation of crossed olivo-cochlear efferents reaching the OHCs.

Acoustic Stimulation

[Evoked otoacoustic emissions in diagnosis of cochlear hearing disorders].

The authors consider the possibility of routine use of evoked otoacoustic emissions (EOE) in diagnosis of sensory hearing loss by comparison of EOE curves with relative curves obtained by pure tone audiometry. 180 ears with sensory hearing loss of different aetiologies were examined. EOE were obtained by application of Bray and Kemp's Evoked Otoacustic Measurement Package (ILO88). The results obtained show a close correlation between presence of EOE and real hearing losses of different frequencies obtained by pure tone audiometric evaluation. We could detect no EOE with hearing losses over 50 dB HL at 500 Hz, 40 dB HL at 1000 Hz, 50 dB HL at 2000 Hz and 85 dB HL at 4000 Hz. With a rate of middle hearing loss over 45 dB HL we also did not find EOE for the whole frequency range. On the base of this study, the authors conclude that EOE explore the functional integrity of those parts of the cochlea that correspond to the middle frequencies of hearing range. If EOE are not detectable, statements on the nature and extent of hearing loss on the base of this examination are not valid.

Adolescent

[Prognostic indications within the scope of the selection of cochlear implant patients].

The common selection criteria for cochlear implant patients do not allow any prognostic indication on the final result. On the other hand, some postoperative data (threshold, TDL, dynamic range, duration of deafness) corresponds clearly with the results, some of them also correspond with the preoperative data. Preoperative TDL, dynamic range as well as duration of deafness can therefore be used as suitable prognostic indicators.

Auditory Threshold

Influence of spontaneous otoacoustic emissions (SOAE) on acoustic distortion product input/output functions: does the medial efferent system act differently in the vicinity of an SOAE?

Otoacoustic emission (OAE) generation mechanisms reside in the active micromechanical properties of the organ of Corti, and especially in the outer hair cells (OHCs). OHCs are strongly innervated by medial efferent olivo-cochlear fibres. Decrease of the intensity of transiently evoked otoacoustic emissions (TOAEs) and modification of spontaneous otoacoustic emissions (SOAEs) during acoustic stimulation of the contralateral ear have already been shown in humans. Similar results were obtained in guinea pigs with a decrease of 2F1-F2 acoustic distortion products (DPOAEs) and a suppression of the effect with sectioning of the floor of the fourth ventricle. The present study sought to investigate the influence of contralateral auditory stimulation on DPOAEs recorded in humans. It shows a decrease in DPOAE intensity for all frequencies, at levels above 45 dB SPL of contralateral broad band noise. This effect was found at levels of contralateral BBN well below the acoustic reflex threshold, and in subjects without acoustic reflex. Moreover, the influence of transcranial transmission could be ruled out since no effect was found when contralateral BBN applied to the altered ear of totally unilaterally deaf patients. Thus, the contralateral acoustic stimulation effect on DPOAEs provides a new means of functional exploration of the medial efferent system in humans. The effect obtained is more ample at low primary frequency levels. Moreover, as DPOAEs are known to be stronger and to show more irregular input/output function patterns in the vicinity of an SOAE, the influence of contralateral auditory stimulation was studied for DPOAEs recorded at 10 Hz, 50 Hz and 150 Hz from an SOAE frequency.

Acoustic Stimulation

Cochlear microphonics and recruitment.

In this study, bilateral cochlear microphonics (CM) were evoked by tone burst simultaneously. A speaker was put in head-food axis 2 m from the mid-point of a given line connecting the bilateral external meatus. Five normal persons and 68 cases (34 cases of Meniere's disease, 27 cases of sudden hearing loss, and 7 cases of low-tone sensory hearing loss without vertigo) with unilateral sensory hearing loss and recruitment, in addition to 2 cases of bilateral Meniere's disease with recruitment were examined. CM shifted in normal and hearing loss ears and was absent in profound and totally deaf ears. When recruitment was present, CM at corresponding frequencies were enlarged and prolongated in 60 cases. Some of the enlarged and prolongated CM decayed slowly, others quickly. Meanwhile the CM of the opposite normal ear decreased obviously. The presence of enlarged and prolongated CM may indicate an increase of abnormal excitability of the hair cells caused by some pathological stimulations. This would cause excitability of the hair cells in the opposite cochlea to be inhibited by the effect of the efferent system. In such a condition, the patients complained that the stimulating sound was heard louder in the disordered ear than that in the opposite normal ear. CM was slightly enlarged during sleep.

Adult

Middle-ear response in the chinchilla and its relationship to mechanics at the base of the cochlea.

The responses of the malleus and the stapes to sinusoidal acoustic stimulation have been measured in the middle ears of anesthetized chinchillas using the Mössbauer technique. With "intact" bullas (i.e., closed except for venting via capillary tubing), the vibrations of the tip of the malleus reach a maximal peak velocity of about 2 mm/s in responses to 100-dB SPL tones in the frequency range 500-6000 Hz; vibration velocity diminishes toward lower frequencies with a slope of about 6 dB/oct. Opening the bulla widely increases the responses to low-frequency stimuli by as much as 16 dB. At low frequencies, malleus response sensitivity with either open or intact bullas far exceeds all previous measurements in cats and matches or exceeds such measurements in guinea pigs. Whether measured in open or intact bullas, phase-versus-frequency curves closely approximate those predicted from the magnitude-versus-frequency curves by minimum phase theory. The stapes responses are similar to those of the malleus, except that stapes response magnitude is lower, on the average, by 7.5 dB at frequencies below 2 kHz and 10.7 dB at 2 kHz and above. Comparison of the responses of the middle ear with those of the basilar membrane at a site 3.5 mm from the stapes indicates that, at frequencies below 150 Hz, the basilar membrane displacement is proportional to stapes acceleration. At frequencies between 150 and 2000 Hz, basilar membrane displacement is proportional to stapes velocity.

Acoustic Impedance Tests

The representation of the spectra and fundamental frequencies of steady-state single- and double-vowel sounds in the temporal discharge patterns of guinea pig cochlear-nerve fibers.

Psychophysical results using double vowels imply that subjects are able to use the temporal aspects of neural discharge patterns. To investigate the possible temporal cues available, the responses of fibers in the cochlear nerve of the anesthetized guinea pig to synthetic vowels were recorded at a range of sound levels up to 95 dB SPL. The stimuli were the single vowels /i/ [fundamental frequency (f0) 125 Hz], /a/ (f0, 100 Hz), and /c/ (f0, 100 Hz) and the double vowels were /a(100),i(125)/ and /c(100),i(125)/. Histograms synchronized to the period of the double vowels were constructed, and locking of the discharge to individual harmonics was estimated from them by Fourier transformation. One possible cue for identifying the f0's of the constituents of a double vowel is modulation of the neural discharge with a period of 1/f0. Such modulation was found at frequencies between the formant peaks of the double vowel, with modulation at the periods of 100 and 125 Hz occurring at different places in the fiber array. Generation of a population response based on synchronized responses [average localized synchronized rate (ALSR): see Young and Sachs [J. Acoust. Soc. Am. 66, 1381-1403 (1979)] allowed estimation of the f0's by a variety of methods and subsampling the population response at the harmonics of the f0 of the constituent vowel achieved a good reconstruction of its spectrum. Other analyses using interval histograms and autocorrelation, which overcome some problems associated with the ALSR approach, also allowed f0 identification and vowel segregation. The present study has demonstrated unequivocally that the timing of the impulses in auditory-nerve fibers provides copious possible cues for the identification of the fundamental frequencies and spectra associated with each of the constituents of double vowels.

Animals