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Protein profile of pepsin-digested carious and sound human dentine.

The purpose of this study was to describe the protein profile of pepsin-digested carious and sound dentine using sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE). Carious and sound dentine powder was decalcified using 10% EDTA at pH 7.4 for 48 h. The decalcified pellet was digested using pepsin at pH 2 under sequenced conditions: at 4 degrees C for 24 h, a further 24 h at 23 degrees C, and finally for 24 h at 37 degrees C. After every step, the soluble fraction was separated by centrifugation and analyzed in 15% SDS-PAGE. Two bands at 56 and 62 kDa could be observed in carious dentine digests and were considered specific carious bands. Similar bands could be observed in sound dentine samples, but only after pepsin digestion at higher temperatures (23 degrees C and 37 degrees C). Pepsin digests non-helical collagen and the triple helix structure of collagen is lost when the temperature rises. The bands at 56 and 62 kDa in sound dentine specimens thus represent pepsin-cleaved collagen. There is a possibility that the specific carious bands in carious dentine represent collagen decomposed in a manner similar to the way pepsin digests native dentine collagen at 23 degrees C and 37 degrees C.

Collagen↗

Sound-evoked postural responses in normal subjects.

A pattern of sound-induced paroxysms of the eye and head and other spinal motor neuron synkinesis (Tullio's phenomenon) in human subjects always implies either a pathological contiguity of the tympano-ossicular chain and membranous labyrinth or a dehiscence of the bone overlying the superior semicircular canal. However, it has become clear in the last decade that sound-evoked vestibular stimulation is not only a sign of disease but also a physiological phenomenon, The examination of such physiologically sound-induced vestibular (saccular) responses contributes today to the clinical testing of the vestibular organ, mainly in the form of vestibular-evoked myogenic potentials. In this study it was observed that, in a group of 20 normal subjects, a 500 Hz tonal stimulus of high intensity (105 dB HL = 118.5 dB SPL), applied monoaurally, elicited postural responses. Each subject was studied under 4 different conditions: (i) head facing forwards, eyes open; (ii) head facing forwards, eyes closed; (iii) head rotated approximately 90 degrees to the right, eyes closed: and (iv) head rotated approximately 90 degrees to the left, eyes closed. Body sway, measured using a force platform, was recorded in all subjects, with eyes either open or closed. Postural responses, which were also elicited with a 250 Hz tonal stimulus, were not observed with a tone of 2000 Hz, with legs slightly flexed or with binaural stimulation. The postural sway (head facing forwards, eyes open or closed) was in a lateral direction towards the stimulated ear: with the stimulus applied to the right ear the subject had postural sway towards the right, with the stimulus applied to the left ear towards the left. When the head was rotated approximately 90 degrees sideways and the stimulus was given facing forwards (i.e. head rotated contralaterally to stimulated ear) the postural sway was in a forward direction; when the head was rotated approximately 90 degrees sideways and the stimulus was given facing backwards (i.e. head rotated ipsilaterally to stimulated ear) the postural sway was in a backward direction. The mean values (mm) of body sway obtained with the head facing forwards and the eyes closed were higher than those with the eyes open (21.7 and 22.8 vs 15.7 and 14.7 for the right and left ears, respectively); higher mean values were obtained with the head turned to the side contralateral to the ear stimulated and the eyes closed (29.3 and 24.8 for the right and left ears, respectively). Under this condition the body sway was mainly in a forward direction. The sound-evoked vestibulopostural reflex seems to be a useful test for exploring the saccular function and, as a click-evoked vestibulocollic reflex, can be considered a physiological Tullio phenomenon.

Acoustic Stimulation↗

Sensitivity to bone-conducted sound: excitation of the mastoid vs the teeth.

The sensitivity of nine subjects to bone-conducted sound was measured at three positions: osseointegrated percutaneous titanium implants in the temporal bone, the skin-covered mastoid and the teeth. Voltage levels supplied to a bone-anchored hearing aid (BAHA) transducer and to an Oticon bone-transducer were measured and the thresholds obtained at the three positions were compared. Using the mechanical impedance of the teeth, the parameters of a first order model for the vibration transmission through the teeth was calculated. Also, the equivalent force thresholds were calculated from the voltage threshold levels. The sensitivity to bone-conducted sound, for both voltage and force thresholds, conformed fairly well at the three positions for frequencies below 1 kHz; however, above 1 kHz, bone-conducted sound applied at the titanium implant becomes more sensitive than at the two other positions investigated. It was concluded that the teeth can be used for the application of bone-conducted sound, in particular for pre-operative assessment of a BAHA and to facilitate service and quality control of such a hearing device.

Adult↗

Control of hearing-aid saturated sound pressure level by frequency-shaped output compression limiting.

To fit a hearing aid successfully, it is important to set the Saturated Sound Pressure Level (SSPL) or Maximum Power Output (MPO) appropriately. The SSPL should be low enough to prevent sounds from being amplified to uncomfortable loudness, and yet high enough to maximize speech intelligibility and signal quality. To help attain an optimum SSPL setting, a novel output compression limiting scheme, with shapable MPO (ShaMPO), has been devised. In ShaMPO, the SSPL is shaped across frequencies in accordance with the individual user's loudness discomfort levels (LDLs). The contributions of different frequency regions to loudness are controlled by summing the amplified signal power relative to the LDLs across frequencies, and using this signal to control a wideband compressor. This scheme and a conventional output compression limiting (AGCo) scheme have been implemented in a digital hearing aid. Ten subjects, with moderately-severe to profound sensorineural hearing losses, participated in a study comparing speech intelligibility and listening comfort for the two schemes. Results showed that there were no significant differences in the speech perception scores between AGCo and ShaMPO, even when the speech was presented at 80 dBA, at which level both schemes were in compression much of the time. However, an examination of how subjects selected the SSPL for the two schemes revealed that, in many instances, AGCo would permit some sounds with compact spectra to be amplified above LDL, whereas ShaMPO would not. Thus the ShaMPO scheme can improve listening comfort for some intense sounds without a loss of speech intelligibility. In contrast, half the subjects found speech at 80 dBA to be uncomfortably loud when listening through their own aids.

Aged↗

Suppressed responses to self-triggered sounds in the human auditory cortex.

Humans are assumed to predict the sensory consequences of their own actions by means of forward models that enable discrimination between self-produced and external sensory signals. Here we tested whether responses in the human auditory cortex would differ to self-triggered versus externally triggered tones. The responses were recorded with a whole-scalp neuromagnetometer from 12 healthy subjects who either themselves triggered a tone by pressing a button once every 5 s or passively listened to externally triggered tones, presented in an identical sound sequence. Sources of the auditory N100m responses, peaking approximately 90 ms after sound onset in the supratemporal auditory cortex, were significantly weaker to self-triggered than to externally triggered sounds (suppressions 24 +/- 7% and 18 +/- 4% in the left and right hemispheres, respectively). These results support the existence of a forward model that predicts the auditory consequences of the subject's own motor acts on the environment--even with a tool--and thereby enables discrimination between self-produced and external sounds.

Acoustic Stimulation↗

Anatomical correlates of foreign speech sound production.

Previous work has shown a relationship between brain anatomy and how quickly adults learn to perceive foreign speech sounds. Faster learners have greater asymmetry (left>right) in parietal lobe white matter (WM) volumes and larger WM volumes of left Heschl's gyrus than slower learners. Here, we tested native French speakers who were previously scanned using high-resolution anatomical magnetic resonance imaging. We asked them to pronounce a Persian consonant that does not exist in French but which can easily be distinguished from French speech sounds, the voiced uvular stop. Two judges scored the goodness of the utterances. Voxel-based morphometry revealed that individuals who more accurately pronounce the foreign sound have higher WM density in the left insula/prefrontal cortex and in the inferior parietal cortices bilaterally compared with poorer producers. Results suggest that WM anatomy in brain regions previously implicated in articulation and phonological working memory, or the size/shape of these or adjacent regions, is in part predictive of the accuracy of speech sound pronunciation.

Adolescent↗

Measurement of the speed of sound in follicular fluid.

BACKGROUND: Measurement of ovarian follicles by ultrasound is common practice in fertility treatment. However, the effect of the speed of sound is not taken into account. We present results from a study aimed at measuring this. METHODS: The speed of sound was measured in samples of follicular fluid aspirated from patients undergoing fertility treatment. The transmitted and received pulses from a single element ultrasound transducer were recorded using a digital oscilloscope for a pulse passed through a sample of the fluid. The distance over which the pulse travelled was known from calibration with pure water. Variation with temperature was investigated in the range 25-45 degrees C. Dependence on ultrasound frequency, patient and time from aspiration were also investigated. RESULTS: The speed of sound in follicular fluid was found to be 1550+/-3 m/s at 37.3 degrees C using 5.0 MHz ultrasound. The speed varied from 1528+/-3 m/s at 24.8 degrees C to 1561+/-3 m/s at 44.8 degrees C. Variation with patient, time and frequency were not detected. CONCLUSION: The speed of sound in follicular fluid at body temperature is 1550 m/s. This small difference from the speed assumed by the ultrasound machine corresponds to the systematic bias in volume measurement evident in previously published results.

Biopsy, Needle↗

Reducing noise damage by using a mid-frequency sound conditioning stimulus.

Sound conditioning guinea pigs to a 6.3 kHz tone at 78 dB SPL for either 13 or 24 days provides significant physiological (auditory brain stem responses, ABR; and distortion product otoacoustic emissions, DPOAE) and morphological (cochleograms) protection against a subsequent traumatic exposure (6.3 kHz, 100 dB SPL for 24 h) delivered 2 h after sound conditioning. Threshold shifts (ABR, DPOAE) were significantly reduced and the degree of hair cell loss was minimal. When a 1 week pause was given between the end of the sound conditioning and the traumatic exposure, protection was still observed, but to a lesser degree. These findings demonstrate that mid-frequency sound conditioning protects against noise trauma and that the protective effect is maintained for at least 1 week.

Acoustic Stimulation↗

Basal forebrain stimulation changes cortical sensitivities to complex sound.

Experience affects how brains respond to sound. Here, we examined how the sensitivity and selectivity of auditory cortical neuronal responses were affected in adult rats by the repeated presentation of a complex sound that was paired with basal forebrain stimulation. The auditory cortical region that was responsive to complex sound was 2-5 five times greater in area in paired-stimulation rats than in naive rats. Magnitudes of neuronal responses evoked by complex sounds were also greatly increased by associative pairing, as were the percentages of neurons that responded selectively to the specific spectrotemporal features that were paired with stimulation. These findings demonstrate that feature selectivity within the auditory cortex can be flexibly altered in adult mammals through appropriate intensive training.

Acoustic Stimulation↗

Event-related potential correlates of sound duration: similar pattern from birth to adulthood.

The effects of sound duration on event-related potentials (ERP) were studied in newborns and adults. Increasing tone duration from 200 to 300 ms led to the enhancement of the N2 peak amplitude, whereas two peaks became distinguishable in the N2 response elicited by 400 ms long tones. The sound-duration related ERP changes most likely reflect contribution from the sustained potential, although the observed results can also be explained by assuming the elicitation of a sound-duration sensitive frontocentrally negative ERP component (duration-sensitive N2; DN2). The pattern of duration-related changes observed in newborn infants was very similar to that in adults, regardless of the structural differences between adult and infant ERPs. The results suggest that sound duration is processed already at birth in a similar way as in adulthood.

Acoustic Stimulation↗

The newborn human brain binds sound features together.

To process a stimulus as a holistic entity, the human brain must be able to conjoin its different features. Previous evidence suggests that this ability emerges during the first months of life, implying its considerable dependence on postnatal development. We recorded human newborn (1-3 days of age) electrical brain responses to frequently occurring (standard) sounds and to rarely occurring (deviant) sounds in a series. Responses to deviants differed from those to standards despite the fact that only the combination of sound frequency and intensity could be used as a cue for discriminating between these sound types. Our finding suggests that the human brain is ready for auditory feature binding very soon after birth.

Acoustic Stimulation↗

Speech-sound discrimination in neonates as measured with MEG.

Magnetic brain responses to speech sounds were measured in 10 healthy neonates. The stimulation consisted of a frequent vowel sound [a:] with a steady pitch contour, which was occasionally replaced by the vowel [i:] with a steady pitch, or the vowel [a:] with a rising pitch, manifesting a change of intonation. The magnetic mismatch-negativity response (MMNm) was obtained and successfully modelled to the speech sound quality change in all infants and to the intonation change in 6 infants. The present results indicate that auditory-cortex speech-sound discrimination may well be studied with magnetic recordings as early as in newborn infants.

Acoustic Stimulation↗

Comparison of two hearing aid receiver-amplifier combinations using sound quality judgments.

Sound quality judgments were obtained on two binaural pairs of laboratory hearing aids with similar battery drain. One pair had a traditional low-current-drain "starved Class A" output stage. The other had a new (at the time) "Class D" output stage. Speech and music reproduction was rated, for seven input levels between 70 and 100 dB SPL, on an overall quality scale by juries of normal-hearing and hearing-impaired subjects. The same subjects also were asked to assign a dollar value to each condition by answering the question "What would you pay for a hearing aid that sounded like that?" Both subject groups rated the hearing aids with the Class D output stage as having superior sound quality across a variety of input levels and test materials, consistent with objective distortion measurements. On the average, each one-percentage point increase in sound quality rating corresponded to a $6.75 increase in perceived value in these experiments.

Adult↗

The effects of broadband noise masking on cortical event-related potentials to speech sounds /ba/ and /da/.

OBJECTIVE: To systematically investigate in normal-hearing listeners the effects of decreased audibility produced by broadband noise masking on the cortical event-related potentials (ERPs) N1, N2, and P3 to the speech sounds /ba/ and /da/. DESIGN: Ten normal-hearing adult listeners actively (button-press response) discriminated the speech sounds /ba/ and /da/ presented in quiet (no masking) or with broadband masking noise (BBN), using an ERP oddball paradigm. The BBN was presented at 50, 60, and 70 dB SPL when speech sounds were presented at 65 dB ppe SPL and at 60, 70 and, 80 dB SPL when speech sounds were presented at 80 dB ppe SPL. RESULTS: On average, the 50, 60, 70, and 80 dB SPL BBN maskers produced behavioral threshold elevations of 18, 25, 35, and 48 dB (average for 250 to 4000 Hz), respectively. The BBN maskers produced significant decreases (relative to quiet condition) in ERP amplitudes and behavioral discriminability. These decreases did not occur, however, until the noise masker intensity (in dB SPL) was equal to or greater than the speech stimulus intensity (in dB ppe SPL), that is, until speech to noise ratios (SNRs) were < or = 0 dB. N1 remained present even after N2, P3, and behavioral discriminability were absent. In contrast to amplitudes, ERP and behavioral latencies showed significant decreases at higher (better) SNRs. Significant latency increases occurred when the noise maskers were within 10 to 20 dB of the stimuli (i.e., SNR < or = 20 dB). The effects of masking were greater for responses to /da/ compared with /ba/. Latency increases occurred with less masking for N1 than for P3 or behavioral reaction time, with N2 falling in between. CONCLUSIONS: These results indicate that decreased audibility as a result of masking affects the various ERP peaks in a differential manner and that latencies are more sensitive indicators of these masking effects than are amplitudes.

Adult↗

Stapes prosthesis attachment: the effect of crimping on sound transfer in otosclerosis surgery.

OBJECTIVES/HYPOTHESIS: Although in stapes surgery successful hearing improvement may be achieved in the majority of patients, unsatisfactory closure of the air-bone gap can be recorded. One of many reasons for unexpected failures of stapes surgery may be the insufficient crimping of a stapes prosthesis onto the incus. The objectives of the study were to assess the amount of sound transmission loss in response to the quality of prosthesis crimping and to identify a required loop attachment pattern to obtain good sound transmission results. STUDY DESIGN: Experimental. METHODS: A temporal bone model was developed to measure the sound transmission properties between incus and prosthesis on 17 fresh human temporal bones. The attachment of a titanium stapes piston was assessed without crimping, followed by loose crimping and tight fixation to the incus, using scanning laser Doppler interferometry, endoscopic photography, micro grinding technique, and scanning electron microscopy. An algorithm had to be developed to simulate acoustical stimulation using electromechanical stimulation. RESULTS: Optimal tight crimping of the stapes piston revealed consistent good sound transfer function ranging from 0 to 7 dB loss, and loss remained, on average, at 2 dB. The mean transmission losses for conditions of loose crimping and no crimping were surprisingly small (within 10 dB). However, these unusual crimping conditions allowed a wide range of losses up to 28 dB. A close coupling at least at two opposite points was obligatory to obtain consistently good results. CONCLUSIONS: Perfect hearing reconstruction necessitates ideal crimping of a prosthesis to obtain consistently good results. However, the final functional gain depends on many different intraoperative and postoperative factors.

Acoustic Stimulation↗

Presbyopia and velocity of sound in the lens.

The elastic properties of lens matter change with age and this contributes to presbyopia. The changes in elasticity of lens matter could be the result of a change in water and soluble proteins (1) or a change in lens fiber cytoskeleton and membranes (2). If it is caused by (1) then the velocity of sound in the lens should change with age. If it is caused by (2) the velocity of sound in the lens will not change. Using the technique of continuous ultrasonographic biometry, the velocity of sound in clear lenses was measured in vivo in a group of 24 healthy subjects aged 15 to 45 years with a visual acuity of 6/6 or better. In this group maximum accommodative amplitude decreased with age. It was found that, despite the occurrence of presbyopia, the velocity of sound did not change with age. Our results support the hypothesis that age-related changes in lens fiber cytoskeleton and membranes are responsible for the change in elastic properties of lens matter and thus contribute to presbyopia.

Accommodation, Ocular↗

Attenuation of cerebral oxygen toxicity by sound conditioning.

HYPOTHESIS: Sound conditioning might reduce cerebral oxygen toxicity. BACKGROUND: Cerebral oxygen toxicity is related to high levels of reactive oxygen species. Noise-induced hearing loss has been shown to result from ischemia-reperfusion, in which reactive oxygen species play a major role. Repeated exposure to loud noise at levels below that which produces permanent threshold shift prevented noise-induced hearing loss and was associated with significant elevation of the antioxidant enzymes measured in the inner ear. We tested the hypothesis that sound conditioning might reduce cerebral oxygen toxicity. METHODS: Forty-five guinea pigs were prepared for electroencephalography and auditory brainstem recording. The auditory brainstem recording detection threshold was determined to confirm baseline normal hearing. The animals were divided into three equal groups and subjected to the following procedures: Group 1, electroencephalography electrode implantation and auditory brainstem recording only; Group 2, exposure to oxygen at 608 kPa (the latency to the first electrical discharge in the electroencephalogram preceding the appearance of seizures was measured); and Group 3, sound conditioning followed by oxygen exposure. The animals were killed, and the brains were excised and homogenized. Brain levels of superoxide dismutase, catalase, glutathione peroxidase, glutathione transferase, glutathione reductase, glucose-6-phosphate dehydrogenase, and thiobarbituric acid reactive substances were compared among the groups. RESULTS: Latency to the first electrical discharge was compared between Groups 2 and 3, and was found to be significantly longer in Group 3 (27.9 +/- 11 versus 20.4 +/- 7.6 min, p < 0.03). No significant changes were found in brain levels of superoxide dismutase, catalase, glutathione peroxidase, glutathione transferase, glutathione reductase, glucose-6-phosphate dehydrogenase, or thiobarbituric acid reactive substances. CONCLUSION: Our data show that sound conditioning prolongs the latency to oxygen-induced convulsions. This effect was not accompanied by significant changes in whole-brain antioxidant enzyme activity or the magnitude of lipid peroxidation.

Animals↗

Organization of sequential sounds in auditory memory.

A repeating five-tone pattern was presented at several stimulus rates (200, 400, 600, and 800 ms onset-to-onset) to determine at what temporal proximity the five-tone repeating unit would be represented in memory. The mismatch negativity component of event-related brain potentials was used to index how the sounds were organized in memory when participants had no task with the sounds. Only at the 200-ms onset-to-onset pace was the five-tone sequence unitized in memory. At presentation rates of 400 ms and above, the regularity (a different frequency tone occurred every fifth tone) was not detected and mismatch negativity was elicited by these tones in the sequence. The results show that temporal proximity plays a role in unitizing successive sounds in auditory memory. These results also suggest that global relationships between successive sounds are represented at the level of auditory cortices.

Acoustic Stimulation↗