May 2006
Volume 47, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2006
Elevated Retinal Thresholds With a Subretinal Microelectrode Array in a Rabbit Model of Photoreceptor Degeneration
Author Affiliations & Notes
  • L.M. Franco
    University of Louisville, Louisville, KY
    Ophthalmology and Visual Sciences,
  • Y. Katagiri
    University of Louisville, Louisville, KY
    Ophthalmology and Visual Sciences,
  • Y. Yamauchi
    University of Louisville, Louisville, KY
    Ophthalmology and Visual Sciences,
  • D. Jackson
    University of Louisville, Louisville, KY
    Electrical and Computer Engineering,
  • J.F. Rizzo, III
    Ophthalmology, Mass Eye & Ear Infirmary, Boston, MA
    Center for Innovative Visual Rehabilitation, VA Medical Center, Boston, MA
  • O.R. Ziv
    Center for Innovative Visual Rehabilitation, VA Medical Center, Boston, MA
  • H.J. Kaplan
    University of Louisville, Louisville, KY
    Ophthalmology and Visual Sciences,
  • V. Enzmann
    University of Louisville, Louisville, KY
    Ophthalmology and Visual Sciences,
  • Footnotes
    Commercial Relationships  L.M. Franco, None; Y. Katagiri, None; Y. Yamauchi, None; D. Jackson, None; J.F. Rizzo, None; O.R. Ziv, None; H.J. Kaplan, None; V. Enzmann, None.
  • Footnotes
    Support  Veteran Affair's Administration V523P/7278, Research Prevent Blindness
Investigative Ophthalmology & Visual Science May 2006, Vol.47, 3169. doi:
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    • Get Citation

      L.M. Franco, Y. Katagiri, Y. Yamauchi, D. Jackson, J.F. Rizzo, III, O.R. Ziv, H.J. Kaplan, V. Enzmann; Elevated Retinal Thresholds With a Subretinal Microelectrode Array in a Rabbit Model of Photoreceptor Degeneration . Invest. Ophthalmol. Vis. Sci. 2006;47(13):3169.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: : To study the electrophysiological changes in the neurosensory retina (NSR) and the response in the visual cortex of rabbits following iodoacetic acid (IAA) injection causing photoreceptor degeneration.

Methods: : Adult Dutch–belted rabbits were injected intravenously with IAA (20 mg/kg body weight). The electrodes for visual evoked potentials (VEP) and electrical evoked potentials (EEP) were placed on the dura mater overlying the visual cortex. A stroboscope generated the stimulation for the VEP and a 5x5 microelectrode array (MEA), placed in the subretinal space, provided the stimulus for the EEP. Both VEP and EEP were recorded 14 days, 1 month, 3 months and 6 months after IAA injection. Normal rabbits were used as controls.

Results: : The VEP amplitude was significantly diminished after IAA injection compared to control eyes (normal = 260.5 ± 75.1 µV). The lowest amplitude was observed at 14 days (49.7 ± 21.5 µV); however, a statistically significant recovery was observed at 1 month (204.3 ± 127.8 µV), 3 months (179.7 ± 101.0 µV), and 6 months (203.1 ± 41.1 µV). The EEP threshold significantly increased over time after IAA injection (e.g., at 1 month = 53.1 ± 17.9 nC) compared to controls (9.2 ± 2.9 nC) but recovered over time (e.g., at 6 months = 37.5 ± 19.1 nC). Likewise, the VEP amplitude in these eyes showed recovery over the 6 months time interval (control = 345.2 ± 46.1 µV; 1 month = 138 ± 46.7 µV; 6 months = 355 ± 151.9 µV).

Conclusions: : IAA significantly elevated the retinal threshold in a rabbit model of photoreceptor degeneration using a subretinal MEA to elicit an EEP. However, the electrophysiological changes caused by IAA at the dosage used appear to be transient and reversible.

Keywords: electrophysiology: non-clinical • photoreceptors • retinal degenerations: cell biology 
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