scholarly journals Auditory Nerve Fiber Health Estimation Using Patient Specific Cochlear Implant Stimulation Models

Author(s):  
Ziteng Liu ◽  
Ahmet Cakir ◽  
Jack H. Noble
2021 ◽  
Author(s):  
Frank Rattay ◽  
Thomas Tanzer

Abstract Electrodes of a cochlear implant generate spikes in auditory nerve fibers. While the insertion depth of each of the electrodes is linked to a frequency section of the acoustic signal, the amplitude of the stimulating pulses controls the loudness of the related frequency band. The firing efficiency of an auditory nerve fiber, stimulated by a train of pulses varies between 0 and 100%. 100% firing efficiency means every pulse elicits a spike, 50% defines threshold. The dynamic range of an auditory nerve fiber is the range of stimulus intensities that causes a firing probability between 10 and 90%. This ‘electrical’ dynamic range is quite small in comparison to the variation of spiking rates measured during acoustic stimulation. Consequently, an increased dynamic range may improve the quality of auditory perception for cochlear implant users. Electrodes are often placed as close as possible to the center axis of the cochlea. Analysis of simulated auditory nerve firing showed that this placement is disadvantageous for the dynamic range. Five times larger dynamic ranges are expected for electrodes close to the terminal of the dendrite or at mid-dendritic placement.


2020 ◽  
Author(s):  
Eric D. Young ◽  
Jingjing Sherry Wu ◽  
Mamiko Niwa ◽  
Elisabeth Glowatzki

AbstractThe synapse between inner hair cells and auditory nerve fiber dendrites shows large EPSCs, which are either monophasic or multiphasic. Multiquantal or uniquantal flickering release have been proposed to underlie the unusual multiphasic waveforms. Here the nature of multiphasic waveforms is analyzed using EPSCs recorded in vitro in rat afferent dendrites. Spontaneous EPSCs were deconvolved into a sum of presumed release events with monophasic EPSC waveforms. Results include: first, the charge of EPSCs is about the same for multiphasic versus monophasic EPSCs. Second, EPSC amplitudes decline with the number of release events per EPSC. Third, there is no evidence of a mini-EPSC. Most results can be accounted for by versions of either uniquantal or multiquantal release. However, serial neurotransmitter release in multiphasic EPSCs shows properties that are not fully explained by either model, especially that the amplitudes of individual release events is established at the beginning of a multiphasic EPSC, constraining possible models of vesicle release.


Author(s):  
Xiang Yang Zheng ◽  
Donald Henderson ◽  
Sandra L. McFadden ◽  
Da Lian Ding ◽  
Richard J. Salvi

2011 ◽  
Author(s):  
Maria A. Berezina ◽  
John J. Guinan ◽  
Christopher A. Shera ◽  
Elizabeth S. Olson

Sign in / Sign up

Export Citation Format

Share Document