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R Hamernik

Publications and source records attributed to R Hamernik.

10 recordsLinked to original sources

[Impulsive noise: PTS and anatomic correlations].

The EEH (Equal Energy Hypothesis) postulates that permanent hearing loss (PTS) produced by exposure to noise is a function of sound energy of the exposure. The validity of EEH for continuous noise exposure was confirmed by large scale demographic studies and experiments in controlled laboratory setting. However, for impulse noise, EEH may not be as valid. This study was designed to test the applicability of EEH in impulse noise exposure in chinchillas. 9 groups of chinchillas were exposed to impulse noise. The intensity of the impulses (113, 125 and 137 dB SPL) and the rate (900, 3,600 and 14,400 impulses/hour) of the 9 exposure conditions were counterbalanced so that the 9 groups received the same total energy. PTS was obtained at 0.5, 2. and 8.0 kHz, by recording the evoked potentials from a chronic electrode implanted in the inferior colliculus. The cochleas were dissected and evaluated using conventional histological surface preparations and examined through scanning electron microscopy (SEM) employing a JEOL 35 microscopy. In our experimental conditions only the 113 dB SPL exposures were consistent with EEH (PTS less than 20 dB). The 125 dB SPL peak level is a critical value in that the validity of EEH also depends on exposure duration. As duration increases, so does PTS. At a 137 dB SPL peak level, EEH is not applicable. The amount of PTS is higher than 50 dB. It slightly increases when the impulse rate per hour becomes higher. In all cases examined PTS is less at 0.5 kHz than at 2.0 or 8 kHz. In these animals excellent informations concerning the sensory cell losses and cells damage was obtained with SEM.

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Amplitude modulation thresholds in chinchillas with high-frequency hearing loss.

Estimates of auditory temporal resolution were obtained from normal chinchillas using sinusoidally amplitude modulated noise. Afterwards, the animals were exposed to noise whose bandwidth was progressively increased toward the low frequencies in octave steps. The first exposure was to an octave band of noise centered at 8 kHz. Three additional octave bands of noise were subsequently added to the original exposure in order to progressively increase the extent of the high-frequency hearing loss. The first exposure produced a temporary hearing loss of 50 to 60 dB near 8 kHz and elevated the amplitude modulation thresholds primarily at intermediate (128 Hz) modulation frequencies. Successive noise exposures extended the temporary hearing loss toward lower frequencies, but there was little further deterioration in the amplitude modulation function until the last exposure when the hearing loss spread to 1 kHz. The degradation in the amplitude modulation function observed after the last exposure, however, was due to a reduction in the sensation level of the test signal rather than to a decrease in the hearing bandwidth. The results of this study suggest that the high-frequency regions of the cochlea may be important for temporal resolution.

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Ultrastructural changes to the cochlea resulting from impulse noise.

Following impulse noise trauma to chinchillas, observation of plastic-embedded surface preparations of the organ of Corti showed no consistent relationship between cochlear hair cell loss and permanent hearing loss (Hamernik et al. 1980). In some animals there was a loss of hearing when hair cells were present. The cochleas from that experiment were examined with transmission electron microscopy to determine at the ultrastructural level if there was damage to the sensory cells that would explain the change in threshold sensitivity. Ultrastructural changes in cochlear hair cells include an increase in lysosomes, multivesicular bodies, vacuolization of subsurface cisternae, and proliferation of Hensen bodies. These changes are observed in all experimented animals. Alterations to the ultrastructure of the stereocilia vary from animal to animal and on the outer hair cells, the changes include loosening of the stereocilia membranes, loss of stiffness, fusion of the stereocilia and disintegration of the rootlets. These changes are observed only in animals that have a permanent threshold shift after noise trauma.

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Gap detection by the chinchilla.

Five monaural chinchillas were trained with a method of shock-avoidance conditioning to respond to silent intervals, or gaps, in an otherwise noise. The noise was low-pass filtered at either 10 or 6 kHz and presented at six intensities ranging between 23- and 77- dB sound-pressure level (SPL). Gap detection thresholds were determined according to the method of constant stimuli. For both noise bands, gap thresholds were approximately 3 ms at the highest intensity levels and increased to approximately 6 ms at the lowest level. The results obtained from the chinchilla are in general agreement with those obtained from man.

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Neural correlates of sensorineural hearing loss.

Sensorineural hearing loss is characterized by a relatively well defined set of audiological signs and symptoms such as elevated thresholds, abnormally rapid loudness growth, subjective tinnitus, poor speech discrimination, and a reduction in temporal summation of acoustic energy. Knowledge of the underlying neural mechanisms responsible for some of these auditory distortions has progressed substantially within the past 10 yrs as a result of physiological studies on hearing-impaired animals. Some of the important neurophysiological changes relevant to sensorineural hearing loss are reviewed. One important effect associated with sensorineural hearing loss is the broadening of the cochlear filtering mechanism which may influence loudness growth and the perception of complex sounds. The neurophysiological results may also provide new insights in interpreting traditional audiological data and help in developing more refined tests for fitting hearing aids or differentiating patients with sensorineural hearing loss.

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The consistent occurrence of a striated organelle (Friedmann body) in the inner hair cells of the normal chinchilla.

Striated organelles have consistently been observed in electron micrographs of serial sections from the inner hair cells of normal chinchilla cochleas. The striated organelle is located in the infracuticular plate region. It lines the cuticular plate, and the direction, pattern and periodicity of the striations vary along its length. The striated organelle is seen in close association with the cell membrane, smooth endoplasmic reticulum, microtubules and mitochondria. The striated organelle may play an active role in inner hair cell function, and its proliferation under pathological conditions, as observed by others, may be accompanied by alterations in sensitivity of the inner hair cell to stimuli.

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Correlation of audiometric data with changes in cochlear hair cell stereocilia resulting from impulse noise trauma.

In a previous experiment, after chinchillas had been exposed to impulse noise trauma, plastic-embedded surface preparations of the organ of Corti were examined with the light microscope. A consistent relationship between cochlear hair cell loss and hearing loss was not found (Hamernik et al., 1980). In the present study, four cochleas from that experiment were sectioned and examined with the transmission electron microscope to determine if their were consistent patterns of damage to the sensory cells at the ultrastructural level that would more closely correlate with the audiometric data. Alterations of the outer hair cell stereocilia were found when threshold was elevated 15 to 30 dB. The membranes of the stereocilia appeared loose and wrinkled and the stereocilia were no longer erect. In some cases, predominantly in the first row of outer hair cells, stereocilia were missing and in other cases, stereocilia were fused. Within these giant stereocilia, the rootlets of the individual stereocilia had disintegrated. Other alterations in sensory cell ultrastructure, though present, had no consistent pattern and could not be related to changes in hearing thresholds. Only the changes in the outer hair cell stereocilia appeared to correlate with hearing loss and the degree of damage was reflected in the amount of threshold elevation.

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Threshold-duration function of the acoustic reflex in man.

The threshold-duration function of the acoustic reflex was investigated in 5 male and 5 female adult, normal-hearing humans and in 3 adult male subjects with hearing loss of cochlear etiology. Reflex threshold was obtained at stimulus durations of 10, 20, 50, 100, 200, and 500 msec and at frequencies of 500, 1 000, 2 000, 3 000, and 4 000 Hz. Three commercially available acoustic bridges were employed, the Madsen ZO-70 and Grason-Stadler 1720 electroacoustic bridges, and the Grason-Stadler-Zwislocki model 3 mechanical-acoustic bridge. A probe-tone frequency of 220 Hz was used in all measures. The reflex threshold-duration function for normal-hearing subjects was found to encompass a much greater range of intensity than the psychophysically assessed auditory threshold temporal integration function. A sex difference was found which may be explained by subclinical noise-induced cochlear pathology in the male subjects with subsequent truncation of the reflex threshold-duration function. The function was also found to be truncated in the 3 subjects with hearing loss diagnosed to be of cochlear etiology. The implications of these findings for control of stimulus duration in clinical reflex measurement was discussed.

Acoustic Stimulation↗

[Interaction between continuous and impulse noise: anatomic and functional evaluation in relation to the intensity of the exposure].

Interaction between continuous and impulse noise was studied. One group of chinchillas was exposed to octave band of noise of 0.5 kHz 95 dB SPL intensity. Three groups were exposed to impulse noises of 113, 119 and 125 prak SPL emitted at 1 imp/sec, 1 imp/4 sec and 1 imp/16 sec respectively. Three groups were exposed to noise created by a combination of above continuous and impulse noises. All exposures lasted for 5 days. Hearing thresholds were measured in 35 animals using auditory evoked potentials. The combined continuous and impulse noises showed equal energy contents, but the groups exposed to 119 and 125 dB impulse noise intensities developed an exacerbation of PTS and cell hair loss. Therefore, the critical level, under which the damage associated with noise exposure is related to the total noise energy (Equal Energy Hypothesis) was reduced when impulse noise was added to continuous noise.

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[The frequency spectrum in the interaction between continuous and impulse noise: an anatomic functional evaluation].

In industrial setting impulse noise rarely occurs in isolation. Impulses are more often superimposed on a background of continuous noise. Since measurement of peak sound pressure level or energy considerations may not provide a sufficient index of danger to hearing, examining the frequency spectra of the noises appeared to be important. Seven groups of five chinchillas were used in this study. Four groups were exposed to octave bands of noise centered at 0.5, 2 or 4 kHz having intensities of 95, 90 and 86 dB SPL respectively or impulse noise of 113 dB peak SPL applied on time per 1 second. Three groups were exposed to the combination of impulse noise and one of the above continuous noises. Each exposure lasted five days. PTS was calculated on each animal using auditory evoked potentials. The cochleas were dissected and evaluated using conventional histological surface preparation and examined with scanning electron microscopy (SEM) employing a JEOL 35 microscope. The groups exposed to only the impulse or to continuous noise alone developed neither PTS nor hair cell loss. Considerable values of PTS and sensory cell loss were observed in animals exposed to impulse noise in combination with 2 and 4 kHz of continuous noise. This interaction effect increases as the spectral overlapping between the impulse and continuous noise increases. In these animals excellent information concerning the sensory cell losses or cell damage was obtained with SEM. The results of the present study demonstrate that interaction between impulse and continuous noise can indicate increased hazard, which is highly dependent not only upon the total energy of the complex exposure but also on the degree of spectral overlapping between impulse and continuous noise.

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