Graeme Clark Collection
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ItemChronic electrical stimulation of the auditory nerve at high rates: I. Effect on residual hearing [Abstract]( 1996)In addition to direct excitation of auditory nerve fibres, cochlear implant patients with small amounts of residual hearing may receive important additional auditory cues via electrophonic activation of hair cells 1. Before incorporating electrophonic hearing into speech processing strategies, the extent of hair cell survival following cochlear implantation must first be determined. We have recently demonstrated widespread survival of hair cells apical to electrode arrays implanted for periods of up to three years, the present report describes the effects of chronic electrical stimulation on hair cell survival.
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ItemChronic electrical stimulation of the auditory nerve at high rates: II. Cochlear pathophysiology [Abstract]( 1996)A major factor in the improved performance of cochlear implant patients has been the use of high stimulus rate speech processing strategies. While these strategies show clear clinical advantage, we know little of their long-term safety. Indeed, recent studies have indicated that high stimulus rates at intensities above clinical limits, can result in neural damage as a result of prolonged neuronal hyperactivity. The present study was designed to evaluate the effects of chronic electrical stimulation of the auditory nerve at high rates, using intensities within clinical limits.
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ItemSpatial representation of the cochlea within the inferior colliculus of neonatally deafened kittens following chronic electrical stimulation of the auditory nerve [Abstract]( 1995)The orderly tonotopic representation of the cochlea is accurately reproduced within the central auditory system of normal hearing animals. Any degradation of this representation as a result of a neonatal hearing loss or chronic electrical stimulation during development could have important implications for the use of multichannel cochlear implants in young children. In the present study we have used 2-deoxyglucose autoradiography (2-00) to examine the topographic representation of the cochlea within the inferior colliculus (IC) of neonatally deafened kittens following periods of chronic intracochlear electrical stimulation.
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ItemImproved sound processing for cochlear implants( 2002)Four signal processing schemes currently under development aim to improve the perception of sounds/ especially speech, for children and adults using the Nucleus cochlear implant system. The schemes are (1) fast-acting input-signal compression, (2) Adaptive Dynamic Range Optimisation (ADRO), (3) TESM, a scheme that emphasises transients in signals, and (4) DRSP, a strategy that applies different stimulation rates to selected sets of electrodes.
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ItemBrainstem encoding of short voice onset times in natural speech( 2001)An auditory nerve study has shown that short voice onset times (VOTs) in synthetic consonant-vowel syllables are not accurately encoded by the fibres' discharge rate. We have re-examined this issue within the ventral Cochlear nucleus (VCN), using natural speech and a fine-grain analysis of single unit responses. We recorded extracellularly from 93 VCN neurons in rats anaesthetised with urethane (2.5 g/kg ip). After identifying a cell's response type and best frequency (BF), 3 syllables spoken by a male were presented at double rate and 3 intensities (/bεt/, /dεt/, and /gεt/, at 45, 65, and 75 dB SPL). These three syllables differ in their VOTs (the interval between consonant release and the onset of glottal pulses associated with voicing) due to the different points of articulation of the three initial stop consonants. In many neurons (particularly onset cells), these syllables evoked a clear response to consonant release, followed by an interval of inactivity or reduced activity before the periodic response to the vowel's voicing frequency commenced. This interval of reduced or no activity corresponded to a given syllable's VOT. The responses of all cells (BFs: 0.9-19 kHz) to the 9 different syllable-SPL combinations were plotted as Grand Average post-stimulus time histograms. In 8/9 combinations, syllable onset was associated with a statistically significant peak in activity and the next significant peak in discharge rate occurred at the time of voice onset (± I ms). These results indicate that the prominent responses to consonant release and voice onset, produced by the synchronous firing of neurons with a wide range of BFs, accurately encode short VOTs.
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ItemHow much residual hearing is too much?( 2000)The value of cochlear implants as an established clinical option for profoundly hearing-impaired adults and children has been supported by significant research results over a number of years (U.S. National Institutes of Health Consensus Statement 1995). As a direct consequence of the level of benefits shown for cochlear implant users on measures of speech perception, research has focused on investigating whether severely hearing impaired adults and children would be suitable candidates for cochlear implantation. I n considering the candidature of any individual, both medical and audiological suitability are investigated. The primary concern is to establish to what degree the patient would benefit from use of the cochlear implant.
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ItemImplantation of the new nucleus C1-3 receiver stimulator and electrode array [Abstract]( 1997)There is an important need to fix the cochlear implant electrode array at a site close to the cochlea, so that the electrode will not slide out, or be subject to differential movement with growth changes. Fixation sites have been in the region of the posterior root of the zygoma and the floor of the antrum. Fixation has been by Dacron mesh ties platinum wire ties, or clips inserted with-special instruments. Biological cements have previously been tried but found to be toxic. The most ideal site is in the region of the cochleostomy.
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ItemTemporal coding for sound and tempor-spatial patterns of electrical stimulation [Abstract]( 1997)The anterior division of the ventral cochlear nucleus (AVCN) is the first relay station of the auditory pathway. It receives auditory information via the auditory nerves emanating from the cochlea. Electrical stimulation via current cochlear implants [ ] does not lead to responses at the cochlear nucleus that exactly match tho elicited by comparable auditory stimulation. Complex temporal patterns of electrical stimulation may provide a better simulation of the acoustic input.
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ItemIntracellular responses of ventral cochlear nucleus neurones to acoustic stimulation in the rat( 1997)The ventral cochlear nucleus (VCN) is the first relay station of the auditory pathway. Presently, little is known about the acoustically evoked intracellular response of neurones in the VCN. We investigated the effect of acoustic stimulation on neurones in the rat VCN using in vivo intracellular recordings and dye-filling. In male rats anaesthetised with urethane (1.3g/kg i.p) microelectrodes containing 1M potassium acetate, or with 4% neurobiotin, were inserted into the VCN. Stable impalements were made from 37 neurones classified as having a Primary-like (n=13), Primary-like with notch (n=4) and Chopper (n=20) response to acoustic stimulation (50 ms pure tones, 5 ms r/f time, 0.2 Hz repetition).
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ItemIncreased survival of auditory neurones treated with LIF( 1997)Degeneration of spiral ganglion cells (SOC) is one of the most common correlates of sensorineural hearing loss (1). Several lines of evidence show that the continued supply of growth factors is responsible for maintaining auditory neurone integrity (2). In the present study SOC cultures were used as a model of auditory innervation to test the ability of the cytokine leukaemia inhibitory factor (LIF) and the neurotrophin NT -3 to promote neuronal survival individually or in combination. The data demonstrate that LIF promotes the survival of SOC in a concentration-dependent manner, with a significant increase in neuronal survival at concentrations as low as 0.1 ng/ml compared to untreated wells ( p< 0.05), and a maximum neuronal survival at 10 ng/ml. In addition, when used in combination LIF and NT-3 were more effective in promoting neuronal survival than either factor individually, with a significant increase in survival at concentrations of 0.1ng mI[to the power of]-1/0.1 ng mI[to the power of]-1 (LIF/NT-3). To our knowledge this is the first study reporting that LIF has trophic activity on SOC. Moreover, the data suggest that a combination of several growth factors may provide a better approach when developing pharmacological therapies for auditory neuron repair.