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R P Hamernik

Publications and source records attributed to R P Hamernik.

At least 19 recordsLinked to original sources
PubMed1991

The energy spectrum of an impulse: its relation to hearing loss.

Permanent threshold shifts obtained from 242 chinchillas that were exposed to various impulse noise paradigms have been related to the energy spectra of the impulses. The impulses were generated by three different shock tubes that produced impulse noise spectra whose A-weighted energies showed peaks at 0.25, 1, and 2 kHz. The results show that there is an increasing susceptibility to NIPTS as the audiometric test frequency increases from 0.5 to 16 kHz. This increase in susceptibility to NIPTS is further accentuated by approximately 5 to 10 dB for impulses whose spectra peak at 2 kHz.

Animals↗
PubMed1990

A generalized approach to random noise synthesis: theory and computer simulation.

A generalized approach to the synthesis of Gaussian and non-Gaussian random noises as well as purely impulsive waveforms having a preselected amplitude spectrum has been developed. The basic idea behind the synthesis is to construct the amplitude-time waveform from the frequency domain, i.e., from the amplitude and phase spectra. By maintaining a predetermined (reference) amplitude spectrum and performing certain specific manipulations of the phase spectrum within any selected band of frequencies and then applying the inverse discrete Fourier transform (IDFT), peaks in the non-Gaussian random waveform can be constructed from the selected band of frequencies that have been phase manipulated. Entire families of signals can thus be produced having the same energy spectrum, but statistical characteristics that vary along the continuum from Gaussian (skewness = 0 and kurtosis = 3) through non-Gaussian (variable skewness, kurtosis, and crest factor) to purely impulsive (shock/transient) signals. The theoretical background and the results of a series of numerical simulations will be presented which demonstrate the functional relation between various phase spectrum manipulations and the descriptors of the synthesized random noise. The results show that the approach is viable and that the synthesized random waveforms can be easily tailored to simulate a variety of real-world acoustic/vibration signals, e.g., high kurtosis (impulsive) industrial noises, helicopter noises, missile vibrational signals, etc.

Acoustic Stimulation↗
PubMed1989

The quantitative relation between sensory cell loss and hearing thresholds.

On the basis of experimental data obtained from 420 noise-exposed animals (chinchilla), the amount of sensory cell loss has been quantitatively related to the amount of permanent threshold shift at eight audiometric test frequencies between 0.125 and 16 kHz. The noise exposures, which varied extensively in spectrum, intensity and duration, produced permanent threshold shifts that ranged from 0 to 70 dB across a broad range of test frequencies. These data show: (1) consistent outer hair cell losses with less than 5 dB permanent threshold shifts (PTS) across all the test frequencies; (2) the first approximately 30 dB of PTS is established by losses of primarily outer hair cells; (3) in regions of the cochlea that transduce frequencies higher than or equal to 2 kHz, the three rows of outer hair cells show the same degree of loss for a given PTS, while in the 0.5 to 1.0 kHz region of the cochlea, the third row of outer hair cells (OHC) consistently shows less loss than do rows one and two; (4) appreciable inner hair cell (IHC) loss does not begin to appear until PTS exceeds approximately 30 dB; (5) in the virtual absence of OHC, hearing thresholds are least sensitive to IHC loss in the octave band centered at 4 kHz, i.e., the 4 kHz region can be as functional as other areas of the cochlea in spite of a greater amount of damage. The quantitative relation between cell loss and PTS varies as a function of test frequency in an orderly fashion.

Animals↗
PubMed1989

The relation among hearing loss, sensory cell loss and tuning characteristics in the chinchilla.

Evoked-potential tuning curves were obtained on over 150 chinchillas before and after acoustic overstimulation in order to relate the effects of changes in frequency selectivity to sensory cell loss over a wide range of hearing loss. Pre- and post-exposure measures of auditory thresholds and masked thresholds (simultaneous tone-on-tone paradigm) were obtained in each animal at 0.5, 1.0, 2.0, 4.0, 8.0 and 11.2 kHz, using the auditory evoked potential recorded from the inferior colliculus. Three tuning curve variables (Q10dB, low-frequency slope and high-frequency slope) were compared to the amount of noise-induced permanent threshold shift and to the percent sensory cell loss produced by a variety of noise exposures. Based upon large sample averages, frequencies showing permanent threshold shifts in excess of 10 dB also showed statistically significant differences between pre- and post-exposure measures of all three tuning curve variables. Shifts of less than 10 dB were not accompanied by statistically significant changes in the tuning curve variables. The percentage of outer hair cell loss, and percentage change in tuning curve characteristics showed systematic and parallel increases as threshold shifts increased at all probe tone frequencies except 8.0 and 11.2 kHz. In general, the results were consistent in showing that there is a systematic change in the variables which define the quality of tuning as hearing loss progressively increases and that these changes are clearly related to outer hair cell losses.

Acoustic Stimulation↗
PubMed1989

Noise and vibration interactions: effects on hearing.

There is the suggestion in the literature that vibration may potentiate the effects of noise and may thus increase the risk of hearing loss in a variety of exposure situations. However, in human experimental studies, which, by necessity, are limited to low levels of exposure, the effects measured are relatively small. A very limited number of animal studies have also shown an enhanced noise-induced hearing loss in the presence of vibration, but the scope of these studies is limited. The animal studies (chinchilla) that form the basis of this report were performed using a 30-Hz, 3g rms and a 20-Hz, 1.3g rms cage vibration separately and in combination with continuous noise (95-dB, 0.5-kHz octave band) and impact noise (113, 119, or 125 dB peak SPL) exposure paradigms. All exposures lasted for 5 days. The impact noise exposures were designed to have approximately equal total energy. Temporary and permanent threshold shifts were measured using evoked potentials, and sensory cell loss was measured using surface preparation histology. The results obtained from some of the noise/vibration paradigms showed that such exposures can alter some of the dependent measures of hearing. This effect was statistically significant only for the stronger vibration exposure conditions and was evident primarily in the extent of the outer hair cell losses and in the shape of the PTS audiogram.

Animals↗
PubMed1989

Damage of the auditory system associated with acute blast trauma.

This paper reviews the results of several studies on the effects of blast wave exposure on the auditory system of the chinchilla, the pig, and the sheep. The chinchillas were exposed at peak sound pressure levels of approximately 160 dB under well-controlled laboratory conditions. A modified shock tube was used to generate the blast waves. The pigs and sheep were exposed under field conditions in an instrumented hard-walled enclosure. Blast trauma was induced by the impact of a single explosive projectile. The peak sound pressure levels varied between 178 and 209 dB. All animals were killed immediately following exposure, and their temporal bones were removed for fixation and histologic analysis using light microscopy and scanning electron microscopy. Middle ears were examined visually for damage to the conductive system. There were well-defined differences in susceptibility to acoustic trauma among species. However, common findings in each species were the acute mechanical fracture and separation of the organ of Corti from the basilar membrane, and tympanic membrane and ossicular failure.

Animals↗
PubMed1988

Threshold recovery functions following impulse noise trauma.

An analysis of the pure-tone threshold recovery functions obtained from 118 chinchillas exposed to high-level impulse noise showed that there are at least three distinctly different types of recovery function: type I--a recovery function for which the initial threshold shift recovers monotonically with increasing postexposure time; type II--a delayed recovery; i.e., for a period as long as 6 h following removal from noise, the pure-tone threshold remains elevated and stable before thresholds begin to follow a monotonic course of recovery; and type III--the growth function; i.e., over a period of at least 6 h following removal from the noise, pure-tone thresholds continue to get worse before they begin to follow a monotonic course of recovery. There is more permanent threshold shift (PTS), more sensory cell loss, and predictions of PTS and cell loss based upon initial measures of threshold shift are less accurate at those frequencies characterized by a type III recovery process than at those frequencies characterized by a type I recovery process.

Acoustic Stimulation↗
PubMed1979

Auditory nerve activity and cochlear morphology after noise exposure.

Four chinchillas were exposed for 5 days to an octave band of noise centered at 4 kHz and having an SPL of 86 dB. After a recovery period of approximately 6 months, behavioral audiograms were obtained and auditory nerve fiber activity was recorded. The animals were killed and the cochleas embedded in plastic to obtain a surface preparation and 1 mu radial sections of the organ of Corti. Behavioral threshold shifts ranged from 5 to 20 dB at frequencies between 4 and 11 kHz. Auditory nerve fiber thresholds were elevated up to 70 dB for units with characteristic frequencies between 4 and 14 kHz. Units with higher and lower characteristic frequencies had normal thresholds. Cochleagrams showed narrow lesions of inner and/or outer hair cells over approximately a 1 mm distance. A comparison of the three realms of data revealed the following: (1) The greatest threshold shifts from the noise exposure were seen in the single nerve fiber thresholds while the smallest shifts were seen in the behavioral thresholds, (2) the greatest behavioral and neural threshold shifts and greatest cochlear damage occurred 1 octave above the center frequency of the noise exposure, and (3) based on the frequency-place map of the chinchilla cochlea, the range of fibers with elevated thresholds exceeded the extent of the OHC lesion. A number of anatomical changes were seen that effectively increased the extent of the damage found in the chochleagram. These changes included: distortions in the surface topography of the organ of Corti affecting the orientation of IHC; missing pillar cells in the presence of normal OHC and/or IHC and protrusion of the IHC cuticular plate into the subtectorial space.

Animals↗
PubMed1979

Hearing loss from simulated work-week exposure to impulse noise.

Six monaural chinchillas were exposed to a repetitive, reverberant, impulse noise for a total of five days, 8 h per day. The average peak overpressure within the holding cage was 113 dB. The reverberation time (pressure fluctuation envelope within 20 dB of peak) was 160 ms. Auditory thresholds were measured at 0.25, 0.5, 1, 2, 4, and 8 kHz before and after each day's exposure using either the average-evoked response technique or shock avoidance conditioning. After the last exposure, recovery was monitored for five successive days. Final thresholds were obtained starting at 30 days postexposure after which the animals were sacrificed for cochlear histology. The high frequencies (4, 8 kHz) showed a daily median shift of 40 dB and a 27 dB recovery before the following day's exposure. The low frequencies (0.25, 0.5 kHz) were shifted 35 dB after each day's exposure with a 15 dB recovery overnight. Final median audiograms showed little permanent threshold shift. The cochleagrams for two test animals were found to be normal while the remaining four displayed 10%--40% losses in hair cells at specific cochlear sites.

Animals↗
PubMed1978

Discharge patterns in the cochlear nucleus of the chinchilla following noise induced asymptotic threshold shift.

Chinchillas were exposed to an 86 dB SPL octave band of noise centered at 4.0 kHz for 3.5--5 days. The noise elevated the hearing thresholds between 4.0 and 16.0 kHz to between 60 and 75 dB SPL. Measurements from single neurons in the cochlear nucleus revealed abnormalities in the response properties of neurons with characteristic frequencies (CF) above 2.0 kHz. Units above 2.0 kHz had elevated thresholds (between 50 and 90 dB SPL) and broad tuning curves due to a greater loss in sensitivity near CF than at lower frequencies. The tuning curve Q10dB values for high frequency neurons were generally less than 3.0 and approached the Q10dB values for basilar membrane displacement. Spontaneous activity rates in units above 2.0 kHz were also low. In a few units, the threshold for single tone inhibition was significantly lower than that for excitation; the best inhibitory frequencies were always below 2.0 kHz. Two-tone inhibition was present in both low and high threshold neurons, but its strength was not assessed. Cochleagrams obtained 12 hours postexposure revealed discrete hair cell lesions in the basal third of the cochlea. The locations of the lesions were consistent with the frequencies of maximum hearing loss. The behavioral thresholds and the thresholds at CF of the most sensitive units were within 10--15 dB of each other. The results indicate that intense sounds reduce the sensitivity, frequency selectivity and spontaneous activity of units in the cochlear nucleus. The findings are similar to those obtained in auditory nerve fibers with ototoxic drugs and hypoxia.

Acoustic Stimulation↗
PubMed1978

Asymptotic threshold shift in chinchillas exposed to impulse noise.

Five monaural chinchillas were exposed to a repetitive, reverberant, impulse noise for ten days. The impulse-noise source was a mechanized hammer hitting a steel plate at a rate of 1/s. The average, peak over pressure within the holding cage was 113 dB SPL. Auditory thresholds were determined before and after exposure at 0.5, 1, 1.4 2, 2.8, 4, 8, and 16 kHz utilizing shock-avoidance conditioning. During exposure thresholds were monitored on a daily basis at 0.5 and 8 kHz. Within one hour from the start of the exposure, threshold shift at 8 kHz had reached an asymptotic level, while threshold shift at 0.5 kHz leveled off after 24 h of exposure. Asymptotic threshold shift (ATS) levels of both frequencies varied between 30 and 50 dB across animals. Median threshold shift for both frequencies recovered to within 10 dB of normal after 40 days of recovery. Maximum permanent threshold shift (PTS) was at 2 and 2.8 KHZ with median PTS of 17 and 13 dB, respectively. After final thresholds were obtained (50-70 days), the cochleas were examined histologically using the surface preparation technique. A comparison is made between impulse-noise-induced ATS and ATS produced by continuous-noise sources.

Acoustic Stimulation↗
PubMed1975

The role of the middle ear in acoustic trauma from impulses.

Exposure to high intensity impulse noise may produce a wide range of audiometric and histological effects in experimental animals. The objective of this study was to assess the changes in the middle ear mechanism after impulse noise exposure and to relate these changes to the audiometric and histological effects. Nine monaural chinchilla were exposed to either 161 or 166 db peak SPL impulses of 1 msec "A" duration, presented at a rate of 1 per minute for 50 minutes. The conductive mechanism of the chinchilla was assessed using standard clinical measures of static and dynamic impedance before and after the noise exposure. Auditory thresholds were measured before and after noise exposure using the average evoked response (AER) technique. At 30 days post-exposure, the animals were sacrificed for histology. Pre-exposure tympanometry showed that: 1. the total mean impedance of the chinchilla ear is considerably lower than that of man; 2. a method related hysterisis effect is present in both the susceptance and conductance tympanograms; and 3. sedation has a significant effect on the total impedance of the ear and on the shape of the tympanograms. After exposure to high level impulse noise: 1. tympanograms become irregular and double peaked, indicating tympanic membrane stress; 2. for the given exposure, 166 db is the impulse intensity needed to rupture consistently the tympanic membrane; and 3. audiometric and histological data correlate with the tympanometric findings and demonstrate a protective effect of a tympanic membrane rupture on the cochlea.

Animals↗
PubMedDate not supplied

Effects of combinations of sodium salicylate and noise on the auditory threshold.

Thirty-nine monaural chinchillas were used to study the interaction between sodium salicylate and various TTS-producing noise paradigms. Five animals were included in each of the following three groups: 1) sodium salicylate (400 mg/kg) plus 2-4 kHz, 95 dB SPL noise band for one hour; 2) sodium salicylate (400 mg/kg) plus 4 kHz CF octave band noise at 80 dB SPL for 96 hours; and 3) sodium salicylate (400 mg/kg) plus 50 impulses having 50 musec A-duration and 158 dB peak SPL, presented at one per minute. The remaining 24 animals served as various controls in groups exposed to sodium salicylate or the noise paradigm alone. Thresholds were estimated before, during, and after exposure using the AER technique and cochleagrams were mapped for each cochlea 30 days after exposure. When sodium salicylate was combined with the various noise conditions, the maximum TTS values obtained from the combination studies were comparable to those obtained from the single agent producing the greatest TTS at a particular frequency. No consistent alteration in either magnitude or time course of posttreatment threshold shift was found following the combination treatments as compared to the individual agents alone. Hazard to the auditory system resulting from a combination of sodium salicylate and noise was concluded to be no greater than the hazard presented by either agent alone. This result is also substantiated in the histological results.

Animals↗