April 2009
Volume 50, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2009
In vivo Retinal Imaging Using Spectral Domain Ocular Coherence Tomography in the Royal College of Surgeon Rat
Author Affiliations & Notes
  • N. Patel
    Dept of Ocular Biology and Therapeutics, Institute of Ophthalmology, UCL, London, London, United Kingdom
  • P. Lundh
    Dept of Ocular Biology and Therapeutics, Institute of Ophthalmology, UCL, London, London, United Kingdom
  • A. Amado
    Dept of Ocular Biology and Therapeutics, Institute of Ophthalmology, UCL, London, London, United Kingdom
  • P. Coffey
    Dept of Ocular Biology and Therapeutics, Institute of Ophthalmology, UCL, London, London, United Kingdom
  • Footnotes
    Commercial Relationships  N. Patel, None; P. Lundh, None; A. Amado, None; P. Coffey, None.
  • Footnotes
    Support  None.
Investigative Ophthalmology & Visual Science April 2009, Vol.50, 3799. doi:
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      N. Patel, P. Lundh, A. Amado, P. Coffey; In vivo Retinal Imaging Using Spectral Domain Ocular Coherence Tomography in the Royal College of Surgeon Rat. Invest. Ophthalmol. Vis. Sci. 2009;50(13):3799.

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

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Abstract

Purpose: : The objective was to obtain auto-fluorescence, red free, infra-red images and a live cross-sectional spectral domain OCT image of the retina in age matched rodent models of retinal degeneration and trauma.Methodology: Age matched dystrophic and non dystrophic royal college of surgeons’ rats aged 6 months were anaesthetized using a standard protocol. The animals were examined at different time points with imaging performed with the Heidelberg Spectralis device; a machine capable of multi-imaging with high-resolution spectral domain ocular coherence tomography (SD OCT) system that was modified with the addition of a ‘bolt-on’ lens and built for cross-sectional in vivo imaging of rodent retina.

Results: : Depth resolution and the image quality of such new modified SD-OCT systems allow better resolution of invivo rodent retinal layers such as the highly reflective nerve fibre layer, inner and outer retinal layers. The results show significant retinal thinning by mean of 28% in affected areas compared to controls. Autofluorescence imaging in geographical atrophy shows similar findings to advanced changes in the RCS rat retina with regards to focal point sources. These hyperintense areas could be actively ingesting resident microglial cells.

Keywords: imaging methods (CT, FA, ICG, MRI, OCT, RTA, SLO, ultrasound) • retina • imaging/image analysis: non-clinical 
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