Optogenetic cochlear stimulation evokes midbrain activity with near-physiological temporal fidelity
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When hearing fails, stimulation of the auditory nerve by electrical cochlear implants (eCIs) partially restores hearing, with most eCI users achieving open speech understanding. However, the broad current spread from each electrode limits frequency coding and speech understanding in daily situations with background noise. Spatially confined optogenetic stimulation by future optical cochlear implants (oCIs) improves frequency coding but millisecond closing kinetics of channelrhodopsins (ChRs) might limit temporal coding. Here, we evaluated the utility of fast-closing ChR f-Chrimson for processing temporal information in the auditory system of Mongolian gerbils. We recorded neural activity in the inferior colliculus evoked by f-Chrimson-mediated optogenetic stimulation of the cochlea. F-Chrimson enabled energy-efficient stimulation of the auditory pathway at rates ≥150 Hz, outperforming the slower ChR variants CatCh (blue) and ChReef (green). Energy thresholds for activation of the auditory pathway were in the low µJ range, between ChReef (sub-µJ) and CatCh. Dynamic range and frequency selectivity were comparable to previous observations with CatCh and outperformed electrical stimulation. In conclusion, employing fast-gating ChRs harnesses improved spectral coding without degrading temporal coding.
The Paper Explained
Problem
Electrical cochlear implants (eCIs) partially restore speech comprehension in most of 1 million otherwise severely deaf people. However, most CI-users face challenges hearing in daily situations. Spectrally more selective stimulation of the auditory nerve by optical cochlear implants (oCIs) promises to overcome this limitation. However, the closing kinetics of channelrhodopsins (ChR) limit the temporal bandwidth of bionic sound coding. Improving the ChR properties and evaluating temporal coding remain major objectives for developing hearing restoration by oCI.
Results
Here, we evaluate the utility of waveguide-based oCI using the fast-closing ChR Chrimson (f-Chrimson) for encoding of temporal, spectral and intensity information by multi-electrode-array (MEA) recordings from the midbrain. We compare f-Chrimson-mediated bionic coding to acoustic coding as well as to previous data acquired with optogenetic stimulation using other ChRs and with electrical stimulation. F-Chrimson enabled energy-efficient stimulation of the auditory pathway at rates ≥150 Hz, outperforming the slower ChR variants CatCh (blue) and ChReef (green). Intensity and frequency coding were comparable to previous observations with CatCh and outperformed electrical stimulation.
Impact
This study demonstrates near physiological temporal coding with the fast-closing ChR f-Chrimson, indicating that improved spectral coding by oCI is not traded off by poor temporal fidelity.
