Stapedius reflex in industrial impact noise: fatigability and role for temporary threshold shift (TTS).
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Biomedical subjects
Publications and source records attributed to E Borg.
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The fatiguability of the acoustic stapedius muscle reflex in an actual noisy industrial environment was investigated in normal-hearing subjects. In a laboratory situation a small depression was found with a considerable individual variability. The stapedius reflex recovered slowly, approximately as a linear function of time. In a field study on an entire day of exposure in a ship-building yard the reflex depression was on the average 4 dB in response to a stimulation of 2000 Hz 10 min after the end of the workday. This corresponds to less than 8 dB immediately at the end of the exposure.
A review of some short-term and long-term physiological effects of sound on non-auditory body functions is given. It is pointed out that the short-term effects depend closely on the acoustic properties of the sound. Habituation is rapid for steady signals but slow for interrupted ones. Irrelevant, meaningless sound, presented to rats over their life-time in such a way as to simulate an industrial acoustic environment, did not affect blood pressure, life-span or morbidity incidence. As far as the injurious effect of sound on the inner ear is concerned, it was shown that spontaneously hypertensive rats were considerably more susceptible to such impairment than were normotensive ones. Hence sound does not produce hypertension, but susceptibility to ear injury may be greater in hypertensive individuals. The protential role which individual variability in physiological properties of the sound conduction system might play for the observed individual variability in noise-induced hearing loss is also discussed.
The function of the avian middle ear muscle was investigated in the chicken, Gallus gallus (domesticus). The avian species offers excellent conditions for study of middle ear muscle function since it possesses a single middle ear muscle, the stapedius, which is located extracranially. Electromyograms (EMG), measurements of impedance change, and volume change in the middle ear cavity were used to assess the muscle's activity. The results showed that the middle ear muscle of Gallus does not exhibit an acoustic reflex. However, the stapedius is regularly activated during the animal's own vocalization. Measurements of the EMG and volume change showed the stapedial activity to increase systematically with increases in the vocal sound level. The use of volume change as a measure of stapedius function was found to be highly suitable in the present experiments in that it allows for measurements of the magnitude of the stapedius contraction without altering the intact physiological state of the middle ear, and is insensitive to the ambient noise and vocal sounds, that hamper the impedance technique.
The influence of the stapedius muscle contraction on middle ear volume and acoustic impedance was investigated in the chicken, Gallus gallus. The time course of twitch responses to electrical stimulation (measured as volume and impedance changes) was found to be largely independent of the stimulus voltage, having a contraction time of 22 ms and a half-relaxation time of 22 ms. The stapedius muscle was therefore characterized as a fast twitch muscle. Slow contraction properties were also revealed: A summation of responses to repetitive stimulation beginning at 2.5 Hz and a slow decline to baseline were seen in volume and impedance change recordings. The morphological characteristics were consonant with that of a homogeneously fast muscle: Only fibres with high ATPase activity were identified and no fibres with "en grappe" or multiple innervation were observed. The slow characteristics were suggested to be due to visco-elastic elements in the middle ear. The chicken stapedius muscle is suggested to be analogous to both the stapedius and the tensor tympani of mammals.
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Arterial pulsations have been recorded indirectly from the surface of the rat's tail. Slight heating of restrained unanesthetized rats produces vasodilatation and large amplitude pulsations that are influenced by sensory stimuli, in this case, sound. The surface-recorded pulse volume was found to be proportional to pulse pressure, indicating vasoconstriction as the cause of the decline of the pulse amplitude. A one-second noise burst elicited vasoconstriction, the duration of which was proportional to sound level and occurred as low as at hearing threshold. Under the specified conditions, reproducibility was good with no significant habituation both within session, and between sessions with a one week interval. The warming of the rats was found to be critical for the sound-elicited reactions; responses were obtained only within a narrow, individual temperature-range. The possibilities of using tail vasoconstriction for evaluation of hearing was pointed out, as well as for studies of noise effects on peripheral circulation.
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The respective effects of pentobarbital-sodium, enibumal-sodium, urethane, urethane-chloralose and lidocaine on the function of the acoustic middle ear reflex in the rabbit were studied. The response of the middle ear muscles was measured by recording changes in both ears' acoustic impedance when the reflex was elicited by applying pure tone stimuli (2,000 Hz) to the two ears one at a time. In that way both the crossed and the uncrossed reflexes were studied. All the drugs were found to depress the reflex in such a way that a higher sound intensity was required after administration to achieve the same impedance change as before. The effect of the anesthetics was roughly proportional to their known anesthetic power. Lidocaine produced only a slight depression of the reflex. The crossed reflex showed a greater susceptibility to the general anesthetics than did the uncrossed reflex which suggests a greater complexity of the crossed reflex. Because the method of recording the reflex response does not require any surgery and is equally well applicable in unrestrained rabbits and in humans, it is suggested as a way of testing the effect of drugs on the central nervous system.
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