Spiking Characteristics of Network-Mediated Responses Arising in Direction-Selective Ganglion Cells of Rabbit and Mouse Retinas to Electric Stimulation for Retinal Prostheses

Authors
Otgondemberel, YanjinsurenRoh, HyeonheeFried, Shelley, IIm, Maesoon
Issue Date
2021-11
Publisher
IEEE-INST ELECTRICAL ELECTRONICS ENGINEERS INC
Citation
IEEE TRANSACTIONS ON NEURAL SYSTEMS AND REHABILITATION ENGINEERING, v.29, pp.2445 - 2455
Abstract
To restore the sight of individuals blinded by outer retinal degeneration, numerous retinal prostheses have been developed. However, the performance of those implants is still hampered by some factors including the lack of comprehensive understanding of the electrically-evoked responses arising in various retinal ganglion cell (RGC) types. In this study, we characterized the electrically-evoked network-mediated responses (hereafter referred to as electric responses) of ON-OFF direction-selective (DS) RGCs in rabbit and mouse retinas for the first time. Interestingly, both species in common demonstrated strong negative correlations between spike counts of electric responses and direction selective indices (DSIs), suggesting electric stimulation activates inhibitory presynaptic neurons that suppress null direction responses for high direction tuning in their light responses. The DS cells of the two species showed several differences including different numbers of bursts. Also, spiking patterns were more heterogeneous across DS RGCs of rabbits than those of mice. The electric response magnitudes of rabbit DS cells showed positive and negative correlations with ON and OFF light response magnitudes to preferred direction motion, respectively. But the mouse DS cells showed positive correlations in both comparisons. Our Fano Factor (FF) and spike time tiling coefficient (STTC) analyses revealed that spiking consistencies across repeats were reduced in late electric responses in both species. Moreover, the response consistencies of DS RGCs were lower than those of non-DS RGCs. Our results indicate the species-dependent retinal circuits may result in different electric response features and therefore suggest a proper animal model may be crucial in prosthetic researches.
Keywords
STARBURST AMACRINE CELLS; PRIMATE RETINA; MOTION; VARIABILITY; IDENTIFICATION; ACTIVATION; RESOLUTION; DIVERSITY; CIRCUITS; CHANNELS; Retina; Rabbits; Mice; Visualization; Correlation; Bars; Prosthetics; Artificial vision; retinal implant; retinal prosthesis; electrical stimulation; direction-selective RGC
ISSN
1534-4320
URI
https://pubs.kist.re.kr/handle/201004/116214
DOI
10.1109/TNSRE.2021.3128878
Appears in Collections:
KIST Article > 2021
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