Spatially precise activation of the mouse cochlea with a multi-channel hybrid cochlear implant

<i>Objective.</i>Cochlear implants are among the few clinical interventions for people with severe or profound hearing loss. However, current spread during monopolar electrical stimulation results in poor spectral resolution, prompting the exploration of optical stimulation as an alternative approach. Enabled by introducing light-sensitive ion channels into auditory neurons (optogenetics), optical stimulation has been shown to activate a more discrete neural area with minimal overlap between each frequency channel during simultaneous stimulation. However, the utility of optogenetic approaches is uncertain due to the low fidelity of responses to light and high-power requirements compared to electrical stimulation.<i>Approach.</i>Hybrid stimulation, combining sub-threshold electrical and optical pulses, has been shown to improve fidelity and use less light, but the impact on spread of activation and channel summation using a translatable, multi-channel hybrid implant is unknown. This study examined these factors during single channel and simultaneous multi-channel hybrid stimulation in transgenic mice expressing the ChR2/H134R opsin. Acutely deafened mice were implanted with a hybrid cochlear array containing alternating light emitting diodes and platinum electrode rings. Spiking activity in the inferior colliculus was recorded during electrical-only or hybrid stimulation in which optical and electrical stimuli were both at sub-threshold intensities. Thresholds, spread of activation, and threshold shifts during simultaneous hybrid stimulation were compared to electrical-only stimulation.<i>Main results.</i>The electrical current required to reach activation threshold during hybrid stimulation was reduced by 7.3 dB compared to electrical-only stimulation (<i>p</i>< 0.001). The activation width measured at two levels of discrimination above threshold and channel summation during simultaneous hybrid stimulation were significantly lower compared to electrical-only stimulation (<i>p</i>< 0.05), but there was no spatial advantage of hybrid stimulation at higher electrical stimulation levels.<i>Significance.</i>Reduced channel interaction would facilitate multi-channel simultaneous stimulation, thereby enhancing the perception of temporal fine structure which is crucial for music and speech in noise.

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Publication Details

Journal
Journal of Neural Engineering
Published
2025-04-24
DOI
https://doi.org/10.1088/1741-2552/add091
Citations
2
Primary Topic
Photoreceptor and optogenetics research
Type
article
Field-Weighted Citation Impact
1.82

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article

Spatially precise activation of the mouse cochlea with a multi-channel hybrid cochlear implant

David J. Garrett, A. Thompson, Rachael T. Richardson, Ulises A Aregueta Robles et al.
2 citations
Journal of Neural Engineering
Photoreceptor and optogenetics research
1.82
article

Spatially precise activation of the mouse cochlea with a multi-channel hybrid cochlear implant

David J. Garrett, A. Thompson, Rachael T. Richardson, Ulises A Aregueta Robles, James B. Fallon, Elise A. Ajay, Patrick Ruther, Jiang Zhou, Anita Quigley, Ajmal A Azees
article en
2 citations

Abstract

<i>Objective.</i>Cochlear implants are among the few clinical interventions for people with severe or profound hearing loss. However, current spread during monopolar electrical stimulation results in poor spectral resolution, prompting the exploration of optical stimulation as an alternative approach. Enabled by introducing light-sensitive ion channels into auditory neurons (optogenetics), optical stimulation has been shown to activate a more discrete neural area with minimal overlap between each frequency channel during simultaneous stimulation. However, the utility of optogenetic approaches is uncertain due to the low fidelity of responses to light and high-power requirements compared to electrical stimulation.<i>Approach.</i>Hybrid stimulation, combining sub-threshold electrical and optical pulses, has been shown to improve fidelity and use less light, but the impact on spread of activation and channel summation using a translatable, multi-channel hybrid implant is unknown. This study examined these factors during single channel and simultaneous multi-channel hybrid stimulation in transgenic mice expressing the ChR2/H134R opsin. Acutely deafened mice were implanted with a hybrid cochlear array containing alternating light emitting diodes and platinum electrode rings. Spiking activity in the inferior colliculus was recorded during electrical-only or hybrid stimulation in which optical and electrical stimuli were both at sub-threshold intensities. Thresholds, spread of activation, and threshold shifts during simultaneous hybrid stimulation were compared to electrical-only stimulation.<i>Main results.</i>The electrical current required to reach activation threshold during hybrid stimulation was reduced by 7.3 dB compared to electrical-only stimulation (<i>p</i>< 0.001). The activation width measured at two levels of discrimination above threshold and channel summation during simultaneous hybrid stimulation were significantly lower compared to electrical-only stimulation (<i>p</i>< 0.05), but there was no spatial advantage of hybrid stimulation at higher electrical stimulation levels.<i>Significance.</i>Reduced channel interaction would facilitate multi-channel simultaneous stimulation, thereby enhancing the perception of temporal fine structure which is crucial for music and speech in noise.

Journal of Neural EngineeringVol. 22(3)
Bionics Institute (AU), University of Freiburg (DE), The University of Melbourne (AU), UNSW Sydney (AU), St Vincent's Hospital Melbourne (AU), The Royal Victorian Eye & Ear Hospital (AU), MIT University (MK), Bernstein Center for Computational Neuroscience Freiburg (DE), Brain (Germany) (DE), St Vincents Institute of Medical Research (AU), RMIT University (AU)
State Government of Victoria, National Health and Medical Research Council
Peace, Justice and strong institutions
Openalex Percentile: Top 16%
Photoreceptor and optogenetics research
1.82
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