Rahmani et al combined ver005 JRH 121025.pdf (362.45 kB)
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Chronic Delivery of Low-Level Exogenous Current Preserves Retinal Function in Pigmented P23H Rat

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journal contribution
posted on 26.11.2013, 00:00 authored by Safa Rahmani, Les Bogdanowicz, Joel Thomas, John R. Hetling
Diffuse electrical currents delivered to the eye were investigated in a rat model of retinitis pigmentosa for potentially therapeutic effects. Low-level currents were passed between electrodes placed on the cornea and in the mouth during 30-minute sessions two times per week from 4-16 weeks of age. Single-flash electroretinograms (ERG) were recorded and analyzed for amplitude and measures of sensitivity, and basic histology was performed. ERG a-wave amplitudes were slightly greater in treated vs. age-matched controls at 16 wks of age, but the combined thicknesses of the outer nuclear layer and outer segment layer were similar at this age. Treated animals exhibited a significant preservation of b-wave amplitudes, and a striking preservation of rod sensitivity, measured as the stimulus strength required to reach half-saturation of the a-wave. Analysis of the leading edge of the a-wave using a delayed Gaussian function revealed a decrease in the parameter reflecting gain of the phototransduction cascade over the 12-week course of treatment, and no significant change in control animals over the same period. These results suggest that while the exogenous currents failed to preserve the number or gross structure of rods, the responsivity of individual photoreceptors was relatively preserved, perhaps via an increase in efficiency of photon capture (R* / photon). This preserved functionality may delay the retraction of bipolar cell dendrites from degenerating photoreceptors.

Funding

This work was funded by a research contract with OcuMed, Inc., and by a research fellowship and Novak Family Grant from Fight for Sight.

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Publisher Statement

NOTICE: This is the author’s version of a work that was accepted for publication in Vision Research. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Vision Research, Vol 76, (2013) DOI: 10.1016/j.visres.2012.10.016

Publisher

Elsevier

Language

en_US

issn

0042-6989

Issue date

01/01/2013

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