Spatiotemporal characteristics of retinal response to network-mediated photovoltaic stimulation.

Subretinal prostheses aim at restoring sight to patients blinded by photoreceptor degeneration using electrical activation of the surviving inner retinal neurons. Today, such implants deliver visual information with low-frequency stimulation, resulting in discontinuous visual percepts. We measured retinal responses to complex visual stimuli delivered at video rate via a photovoltaic subretinal implant and by visible light. Using a multielectrode array to record from retinal ganglion cells (RGCs) in the healthy and degenerated rat retina ex vivo, we estimated their spatiotemporal properties from the spike-triggered average responses to photovoltaic binary white noise stimulus with 70-μm pixel size at 20-Hz frame rate. The average photovoltaic receptive field size was 194 ± 3 μm (mean ± SE), similar to that of visual responses (221 ± 4 μm), but response latency was significantly shorter with photovoltaic stimulation. Both visual and photovoltaic receptive fields had an opposing center-surround structure. In the healthy retina, ON RGCs had photovoltaic OFF responses, and vice versa. This reversal is consistent with depolarization of photoreceptors by electrical pulses, as opposed to their hyperpolarization under increasing light, although alternative mechanisms cannot be excluded. In degenerate retina, both ON and OFF photovoltaic responses were observed, but in the absence of visual responses, it is not clear what functional RGC types they correspond to. Degenerate retina maintained the antagonistic center-surround organization of receptive fields. These fast and spatially localized network-mediated ON and OFF responses to subretinal stimulation via photovoltaic pixels with local return electrodes raise confidence in the possibility of providing more functional prosthetic vision. NEW & NOTEWORTHY Retinal prostheses currently in clinical use have struggled to deliver visual information at naturalistic frequencies, resulting in discontinuous percepts. We demonstrate modulation of the retinal ganglion cells (RGC) activity using complex spatiotemporal stimuli delivered via subretinal photovoltaic implant at 20 Hz in healthy and in degenerate retina. RGCs exhibit fast and localized ON and OFF network-mediated responses, with antagonistic center-surround organization of their receptive fields.

[1]  S. W. Kuffler Discharge patterns and functional organization of mammalian retina. , 1953, Journal of neurophysiology.

[2]  J. Dowling,et al.  Organization of the retina of the mudpuppy, Necturus maculosus. II. Intracellular recording. , 1969, Journal of neurophysiology.

[3]  D. Baylor,et al.  Mosaic arrangement of ganglion cell receptive fields in rabbit retina. , 1997, Journal of neurophysiology.

[4]  P. Lukasiewicz,et al.  Action Potentials Are Required for the Lateral Transmission of Glycinergic Transient Inhibition in the Amphibian Retina , 1998, The Journal of Neuroscience.

[5]  W R Taylor,et al.  TTX attenuates surround inhibition in rabbit retinal ganglion cells , 1999, Visual Neuroscience.

[6]  A Hofman,et al.  Risk factors for age-related macular degeneration: Pooled findings from three continents. , 2001, Ophthalmology.

[7]  E. Chichilnisky,et al.  Adaptation to Temporal Contrast in Primate and Salamander Retina , 2001, The Journal of Neuroscience.

[8]  E J Chichilnisky,et al.  A simple white noise analysis of neuronal light responses , 2001, Network.

[9]  R. Lund,et al.  Progressive visual sensitivity loss in the Royal College of Surgeons rat: perimetric study in the superior colliculus , 2001, Neuroscience.

[10]  H. Wässle,et al.  Synaptic Currents Generating the Inhibitory Surround of Ganglion Cells in the Mammalian Retina , 2001, The Journal of Neuroscience.

[11]  E. Chichilnisky,et al.  Functional Asymmetries in ON and OFF Ganglion Cells of Primate Retina , 2002, The Journal of Neuroscience.

[12]  A.M. Litke,et al.  What does the eye tell the brain?: Development of a system for the large scale recording of retinal output activity , 2003, 2003 IEEE Nuclear Science Symposium. Conference Record (IEEE Cat. No.03CH37515).

[13]  D. Dacey,et al.  The Classical Receptive Field Surround of Primate Parasol Ganglion Cells Is Mediated Primarily by a Non-GABAergic Pathway , 2004, The Journal of Neuroscience.

[14]  B. Jones,et al.  Retinal remodeling during retinal degeneration. , 2005, Experimental eye research.

[15]  Daniel Palanker,et al.  Design of a high-resolution optoelectronic retinal prosthesis , 2005, Journal of neural engineering.

[16]  Tomomi Ichinose,et al.  Inner and outer retinal pathways both contribute to surround inhibition of salamander ganglion cells , 2005, The Journal of physiology.

[17]  B. Jones,et al.  Retinal remodeling in inherited photoreceptor degenerations , 2003, Molecular Neurobiology.

[18]  Jonathon Shlens,et al.  Spatial Properties and Functional Organization of Small Bistratified Ganglion Cells in Primate Retina , 2007, The Journal of Neuroscience.

[19]  E J Chichilnisky,et al.  Behavioral / Systems / Cognitive Identification and Characterization of a Y-Like Primate Retinal Ganglion Cell Type , 2007 .

[20]  Timothy A. Machado,et al.  Functional connectivity in the retina at the resolution of photoreceptors , 2010, Nature.

[21]  Joseph F Rizzo,et al.  Selective activation of neuronal targets with sinusoidal electric stimulation. , 2010, Journal of neurophysiology.

[22]  Daniel K Freeman,et al.  Multiple components of ganglion cell desensitization in response to prosthetic stimulation , 2011, Journal of neural engineering.

[23]  A. Sher,et al.  A non-canonical pathway for mammalian blue-green color vision , 2012, Nature Neuroscience.

[24]  A. Sher,et al.  Photovoltaic Retinal Prosthesis with High Pixel Density , 2012, Nature Photonics.

[25]  Jessy D. Dorn,et al.  Interim results from the international trial of Second Sight's visual prosthesis. , 2012, Ophthalmology.

[26]  A. Sher,et al.  Photovoltaic retinal prosthesis: implant fabrication and performance , 2012, Journal of neural engineering.

[27]  Mark S Humayun,et al.  Frequency and amplitude modulation have different effects on the percepts elicited by retinal stimulation. , 2012, Investigative ophthalmology & visual science.

[28]  Eberhart Zrenner,et al.  Functional outcome in subretinal electronic implants depends on foveal eccentricity. , 2013, Investigative ophthalmology & visual science.

[29]  K. Mathieson,et al.  Cortical responses elicited by photovoltaic subretinal prostheses exhibit similarities to visually evoked potentials , 2013, Nature Communications.

[30]  D V Palanker,et al.  Holographic display system for restoration of sight to the blind , 2013, Journal of neural engineering.

[31]  Angelika Braun,et al.  Artificial vision with wirelessly powered subretinal electronic implant alpha-IMS , 2013, Proceedings of the Royal Society B: Biological Sciences.

[32]  D. Palanker,et al.  Selectivity of direct and network-mediated stimulation of the retinal ganglion cells with epi-, sub- and intraretinal electrodes , 2014, Journal of neural engineering.

[33]  A. Sher,et al.  Development of Animal Models of Local Retinal Degeneration. , 2015, Investigative ophthalmology & visual science.

[34]  A. Sher,et al.  Photovoltaic restoration of sight with high visual acuity , 2015, Nature Medicine.

[35]  Jessy D. Dorn,et al.  Long-Term Results from an Epiretinal Prosthesis to Restore Sight to the Blind. , 2015, Ophthalmology.

[36]  K. Mathieson,et al.  Performance of photovoltaic arrays in-vivo and characteristics of prosthetic vision in animals with retinal degeneration , 2015, Vision Research.

[37]  E. Callaway,et al.  Anatomical Identification of Extracellularly Recorded Cells in Large-Scale Multielectrode Recordings , 2015, The Journal of Neuroscience.

[38]  Daniel Palanker,et al.  Contrast Sensitivity With a Subretinal Prosthesis and Implications for Efficient Delivery of Visual Information. , 2015, Investigative ophthalmology & visual science.

[39]  J. Weiland,et al.  Improving the spatial resolution of epiretinal implants by increasing stimulus pulse duration , 2015, Science Translational Medicine.

[40]  H. Lorach,et al.  Retinal safety of near infrared radiation in photovoltaic restoration of sight. , 2016, Biomedical optics express.

[41]  S Sekhar,et al.  Tickling the retina: integration of subthreshold electrical pulses can activate retinal neurons , 2016, Journal of neural engineering.

[42]  James D. Weiland,et al.  Retinal stimulation strategies to restore vision: Fundamentals and systems , 2016, Progress in Retinal and Eye Research.

[43]  Xin Lei,et al.  Photovoltaic Pixels for Neural Stimulation: Circuit Models and Performance , 2016, IEEE Transactions on Biomedical Circuits and Systems.

[44]  D. Palanker,et al.  Electronic approaches to restoration of sight , 2016, Reports on progress in physics. Physical Society.

[45]  M. Eickenscheidt,et al.  Subretinal electrical stimulation reveals intact network activity in the blind mouse retina. , 2016, Journal of neurophysiology.

[46]  S Sekhar,et al.  Correspondence between visual and electrical input filters of ON and OFF mouse retinal ganglion cells , 2017, Journal of neural engineering.