Literature DB >> 6737033

Effects of continuous noise backgrounds on rate response of auditory nerve fibers in cat.

J A Costalupes, E D Young, D J Gibson.   

Abstract

This study describes the effects of broadband background noise on the average discharge rate to best-frequency (BF) tones of auditory nerve fibers in the cat. The effects of exposure to long-term continuous noise are compared to the effects of noise gated on and off simultaneously with test tones. Addition of background noise causes a shift of the dynamic portion of tone-evoked rate versus level functions to higher tone intensities. The shift occurs at a mean rate of 0.61 dB of shift for each 1-dB increment in noise level. The rate of shift is independent of best frequency and spontaneous discharge rate. The noise level at which the shift begins is frequency dependent and is consistent with the frequency-dependent bandwidths of auditory nerve fiber tuning curves. The adjustment of the dynamic range shows many similarities to two-tone suppression. Therefore, it is most likely that it is caused by suppression of the response to the BF test tone by energy present in the noise at surrounding frequencies. At high noise levels, the ability of auditory nerve fibers to respond to test tones is limited by the rate response to the noise. As noise level increases, the discharge rate it evokes approaches a fiber's saturation rate and ultimately eliminates the fiber's ability to respond to test tones. Low spontaneous rate fibers, which have been shown to have higher thresholds and wider dynamic range (17,29), are significantly more resistant to saturation by high noise levels. Exposure to broadband noise prior to onset of test tones produces an overall decrement in response rate. This phenomenon is similar to the effects of short-term adaptation (32) and seems to develop independently of the shift of dynamic range. At high noise levels, previous exposure to the noise produces a small dynamic range shift. This effect is similar to that produced by suppression but is smaller. The effect is occluded in continuous noise backgrounds by the adjustment of sensitivity produced by suppression.

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Mesh:

Year:  1984        PMID: 6737033     DOI: 10.1152/jn.1984.51.6.1326

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  80 in total

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Journal:  J Neurophysiol       Date:  2015-08-12       Impact factor: 2.714

2.  The effects of ipsilateral, contralateral, and bilateral broadband noise on the mid-level hump in intensity discrimination.

Authors:  Elin Roverud; Elizabeth A Strickland
Journal:  J Acoust Soc Am       Date:  2015-11       Impact factor: 1.840

3.  The middle ear muscle reflex in the diagnosis of cochlear neuropathy.

Authors:  Michelle D Valero; Kenneth E Hancock; M Charles Liberman
Journal:  Hear Res       Date:  2015-11-30       Impact factor: 3.208

Review 4.  Cochlear synaptopathy in acquired sensorineural hearing loss: Manifestations and mechanisms.

Authors:  M Charles Liberman; Sharon G Kujawa
Journal:  Hear Res       Date:  2017-01-10       Impact factor: 3.208

5.  Noise-induced cochlear synaptopathy in rhesus monkeys (Macaca mulatta).

Authors:  M D Valero; J A Burton; S N Hauser; T A Hackett; R Ramachandran; M C Liberman
Journal:  Hear Res       Date:  2017-07-08       Impact factor: 3.208

6.  The role of broadband inhibition in the rate representation of spectral cues for sound localization in the inferior colliculus.

Authors:  Bradford J May; Michael Anderson; Matthew Roos
Journal:  Hear Res       Date:  2008-01-26       Impact factor: 3.208

7.  Age-related cochlear synaptopathy: an early-onset contributor to auditory functional decline.

Authors:  Yevgeniya Sergeyenko; Kumud Lall; M Charles Liberman; Sharon G Kujawa
Journal:  J Neurosci       Date:  2013-08-21       Impact factor: 6.167

8.  Nonlinear temporal receptive fields of neurons in the dorsal cochlear nucleus.

Authors:  Sharba Bandyopadhyay; Eric D Young
Journal:  J Neurophysiol       Date:  2013-08-28       Impact factor: 2.714

9.  Synaptopathy in the noise-exposed and aging cochlea: Primary neural degeneration in acquired sensorineural hearing loss.

Authors:  Sharon G Kujawa; M Charles Liberman
Journal:  Hear Res       Date:  2015-03-11       Impact factor: 3.208

10.  Sensory Neuron Diversity in the Inner Ear Is Shaped by Activity.

Authors:  Brikha R Shrestha; Chester Chia; Lorna Wu; Sharon G Kujawa; M Charles Liberman; Lisa V Goodrich
Journal:  Cell       Date:  2018-08-02       Impact factor: 41.582

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