April 2010
Volume 51, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2010
Evaluation of the Photopic Negative Repsonse and Oscillatory Potentials in New Zealand White Rabbits With Retrobulbar Optic Neuropathy and Elevated Intraocular Pressure Following Intracameral Injection of 1% Methylcellulose and Vortex Vein Ligation
Author Affiliations & Notes
  • P. P. Ko
    Ophthalmology, Biological Test Center/B Braun, Irvine, California
  • G. Gum
    Ophthalmology, Biological Test Center/B Braun, Irvine, California
  • R. A. P. de Carvalho
    Ophthalmology, Target Theraputic Technology, Irvine, California
  • Footnotes
    Commercial Relationships  P.P. Ko, None; G. Gum, None; R.A.P. de Carvalho, None.
  • Footnotes
    Support  None.
Investigative Ophthalmology & Visual Science April 2010, Vol.51, 5486. doi:
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      P. P. Ko, G. Gum, R. A. P. de Carvalho; Evaluation of the Photopic Negative Repsonse and Oscillatory Potentials in New Zealand White Rabbits With Retrobulbar Optic Neuropathy and Elevated Intraocular Pressure Following Intracameral Injection of 1% Methylcellulose and Vortex Vein Ligation. Invest. Ophthalmol. Vis. Sci. 2010;51(13):5486.

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

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Abstract

Purpose: : The objective of this study was to evaluate the electroretinogram (ERG) photopic negative response(PhNR) & oscillatory potentials(OPs) in three models of retinal ganglion cell(RGC) loss due to traumatic-induced retrobulbar optic neuropathy(TIRON) or increased intraocular pressure (IOP) in New Zealand White rabbits following intracameral injection of 1% Methyl Cellulose or vortex vein ligation.

Methods: : Ten New Zealand White rabbits received in the right eye an intracameral injection of 0.125 mL of 1% methyl cellulose after an equal volume of aqueous humor was collected from a separate intracameral port. In the second group, the right eye had three out of four vortex veins ligated. In the third group, a vascular clamp with pressure of 50g and 125g was applied to six rabbits' right retrobulbar optic nerves for one minute & released. Clinical progression was evaluated by ERG, fundus color photography, fluorescein angiography(FA) & Ocular Coherence Tomography(OCT). ERG, IOP, OCT, fundus color photography, FA & ophthalmic observations were performed at multiple time points throughout the study. All rabbits were scotopically adapted for 60 minutes prior to the ERG procedures. ERGs were recorded with a 20 msec stimulus of scotopic & photopic luminance. ANOVA statistical analysis was performed.

Results: : In eyes with vortex vein ligation, the amplitudes of ERG PhNR and OP had declined progressively over time compared with the baseline. By Day 9, the mean PhNR amplitudes at +5dB decreased by an average of 50% (p=0.0210) and by 30% at +12.5dB (p=0.1625) after vortex veins ligation. In the eyes after intracameral injection, the mean PhNR amplitudes at +5dB decreased by an average of 38% (p=0.1434). After retrobulbar optic nerve clamping, the mean PhNR amplitudes at +5dB decreased by an average of 28% (p<0.05) by day 16. The ERG data showed that the decreased amplitudes of PhNR correlated with the increased IOP & TIRON progression.

Conclusions: : The decreased amplitudes of PhNR & OP indicate the damage at the RGC & inner retinal plexiform layers. These ERG parameters have the potential to monitor in vivo the effect of pharmacological interventions to prevent or slow down cell loss at RGC & inner retinal plexiform layers.

Keywords: ganglion cells • intraocular pressure • optic nerve 
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