|M.Sc Student||Joshua Nehrer|
|Subject||Towards an Ultrasonic Retinal Prosthetic: In Vivo Ultrasonic|
|Department||Department of Biomedical Engineering||Supervisors||Full Professor Shoham Shy|
|Full Professor Kimmel Eitan|
Retinal degenerative diseases, the principal causes of human blindness, are caused by the degeneration of retinal photoreceptors while the remaining cells in the retinal pathways are left mostly intact. Since the retina is an accessible central nervous system structure, it presents a favorable target for low intensity ultrasonic stimulation, which could potentially bypass the degenerated photoreceptors and restore a visual signal via the remaining retinal neurons. Moreover, this signal can be spatially patterned using ultrasound arrays and holographic algorithms. Previously, characterization studies of visual evoked potentials and electrical responses from isolated retinas demonstrated that ultrasonic stimulation is a promising option for stimulating retinal activity. However, direct measurements of the response to non-invasive ultrasonic stimulation of the retina in vivo are still missing.
Here, we examine the effects of US on mouse retinas in vivo for vision restoration using acoustic neurostimulation. A fluorescent calcium indicator of neural activity was introduced into mouse retinas and fluorescence changes were recorded upon application of US. The effect of the various pulse parameters on successful stimulation was investigated and compared. The observed responses included both excitatory and suppressive neural responses to the US stimuli, whose spatial distributions were largely separable. The responses also showed a systematic increase in the change in fluorescence as the PRF increased. Our results demonstrate the ability to modulate retinal activity in vivo and motivate future research that will explore and refine the stimulation protocols and parameters.