|
|
||||||||
1. Micro-electrode recordings were obtained from over 100 single fibres in the cochlear nerve of the pentobarbitone or urethane anaesthetized guinea-pig. The acoustic system was calibrated at the tympanic membrane and threshold sound level measurements so corrected.
2. The minimum thresholds of the fibres approached with 10-20 dB of the behavioural thresholds reported in the literature. Exceptions to this were fibres from preparations where there was evidence of malfunction of the cochlea either from abnormally low perfusion or local damage, and a few high frequency fibres. With these high threshold fibres excepted, the range of thresholds at a given frequency in any one animal was less than 20 dB.
3. The slopes of the low and high frequency cut-offs of the frequencythreshold curves (`tuning curves') within 25 dB of minimum threshold, ranged from 10 to 60 and from 20 to 125 dB/octave respectively for fibres with characteristic frequencies below 2 kHz, increasing to 90-180 and 200-600 dB/octave respectively for fibres with characteristic frequencies at about 8 kHz. These slopes represent the minimum values for the high-frequency cut-offs, which increase towards 1000 dB per octave in some cases at higher levels above threshold. At 30-50 dB above threshold, the low frequency cut-offs become suddenly less steep and approximate to 5 dB per octave.
4. The relative sharpness of the frequencythreshold curves, measured as the `Q10 dB', i.e. the ratio of characteristic frequency to the band width at 10 dB above minimum threshold, ranged from 1 to 4 for fibres with characteristic frequencies below 2 kHz, to 3-15 for fibres with characteristic frequencies near 10 kHz.
5. The slopes and `Q10 dB' measures of the frequencythreshold curves of most of the abnormally high threshold fibres approximated to, or were lower than those of analogous measurements of the guinea-pig basilar membrane vibration patterns.
6. Four fifths of the cochlear nerve fibres had spontaneous discharge rates greater than 1/sec. No consistent relationship was observed between the rate of this activity and response properties, with the exception that nearly half of the high threshold fibres were silent. In these and other respects the response properties to tonal and click stimuli resembled those of cochlear nerve fibres in the cat. In no case was inhibition of the spontaneous discharge by single tones observed.
7. It is concluded that, contrary to earlier reports, the cochlear nerve fibres of the guinea-pig are substantially more frequency selective than the existing measurements of the guinea-pig basilar membrane displacement. In terms of band width, this discrepancy approaches a factor of ten. The finding of a considerable range of band widths within optimal preparations, and frequencythreshold curves approximating to the mechanical functions in fibres from pathological cochleas, provides circumstantial evidence for a physiologically vulnerable sharpening mechanism occurring within the cochlea subsequent to the displacement pattern of the basilar membrane.
This article has been cited by other articles:
![]() |
P. X. Joris, D. H. Louage, and M. van der Heijden Temporal Damping in Response to Broadband Noise. II. Auditory Nerve J Neurophysiol, April 1, 2008; 99(4): 1942 - 1952. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Ashmore Cochlear Outer Hair Cell Motility Physiol Rev, January 1, 2008; 88(1): 173 - 210. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. B. Averbeck and L. M. Romanski Probabilistic Encoding of Vocalizations in Macaque Ventral Lateral Prefrontal Cortex J. Neurosci., October 25, 2006; 26(43): 11023 - 11033. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. J. Kros and M. G. Evans Tuning in to cochlear hair cells J. Physiol., October 1, 2006; 576(1): 7 - 9. [Full Text] [PDF] |
||||
![]() |
K. N. O'Connor, C. I. Petkov, and M. L. Sutter Adaptive Stimulus Optimization for Auditory Cortical Neurons J Neurophysiol, December 1, 2005; 94(6): 4051 - 4067. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. M. Taberner and M. C. Liberman Response Properties of Single Auditory Nerve Fibers in the Mouse J Neurophysiol, January 1, 2005; 93(1): 557 - 569. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Kaur, R. Lazar, and R. Metherate Intracortical Pathways Determine Breadth of Subthreshold Frequency Receptive Fields in Primary Auditory Cortex J Neurophysiol, June 1, 2004; 91(6): 2551 - 2567. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. X. Joris Interaural Time Sensitivity Dominated by Cochlea-Induced Envelope Patterns J. Neurosci., July 16, 2003; 23(15): 6345 - 6350. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. E. N. LeBeau, M. S. Malmierca, and A. Rees Iontophoresis In Vivo Demonstrates a Key Role for GABAA and Glycinergic Inhibition in Shaping Frequency Response Areas in the Inferior Colliculus of Guinea Pig J. Neurosci., September 15, 2001; 21(18): 7303 - 7312. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Robles and M. A. Ruggero Mechanics of the Mammalian Cochlea Physiol Rev, July 1, 2001; 81(3): 1305 - 1352. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. L. Golding, M. J. Ferragamo, and D. Oertel Role of Intrinsic Conductances Underlying Responses to Transients in Octopus Cells of the Cochlear Nucleus J. Neurosci., April 15, 1999; 19(8): 2897 - 2905. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. S. Narayan, A. N. Temchin, A. Recio, and M. A. Ruggero Frequency Tuning of Basilar Membrane and Auditory Nerve Fibers in the Same Cochleae Science, December 4, 1998; 282(5395): 1882 - 1884. [Abstract] [Full Text] |
||||
![]() |
N. Suga, Y. Zhang, and J. Yan Sharpening of Frequency Tuning by Inhibition in the Thalamic Auditory Nucleus of the Mustached Bat J Neurophysiol, April 1, 1997; 77(4): 2098 - 2114. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |