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Noninvasive Ultrasound Retinal Stimulation for Vision Restoration at High Spatiotemporal Resolution. | LitMetric

AI Article Synopsis

  • Retinal degeneration significantly contributes to permanent vision loss, prompting exploration of new treatment strategies like retinal prostheses and optogenetics.
  • Direct ultrasound stimulation has been shown to activate visual neurons in both normal and blind rats, demonstrating its potential effectiveness.
  • The study suggests that this noninvasive approach provides high spatial and temporal resolution, positioning it as a promising alternative for future visual prosthetics in blind patients.

Article Abstract

. Retinal degeneration involving progressive deterioration and loss of function of photoreceptors is a major cause of permanent vision loss worldwide. Strategies to treat these incurable conditions incorporate retinal prostheses via electrically stimulating surviving retinal neurons with implanted devices in the eye, optogenetic therapy, and sonogenetic therapy. Existing challenges of these strategies include invasive manner, complex implantation surgeries, and risky gene therapy. . Here, we show that direct ultrasound stimulation on the retina can evoke neuron activities from the visual centers including the superior colliculus and the primary visual cortex (V1), in either normal-sighted or retinal degenerated blind rats . The neuron activities induced by the customized spherically focused 3.1 MHz ultrasound transducer have shown both good spatial resolution of 250 m and temporal resolution of 5 Hz in the rat visual centers. An additional customized 4.4 MHz helical transducer was further implemented to generate a static stimulation pattern of letter forms. . Our findings demonstrate that ultrasound stimulation of the retina is a safe and effective approach with high spatiotemporal resolution, indicating a promising future of ultrasound stimulation as a novel and noninvasive visual prosthesis for translational applications in blind patients.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10521738PMC
http://dx.doi.org/10.34133/2022/9829316DOI Listing

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