June 2017
Volume 58, Issue 8
Open Access
ARVO Annual Meeting Abstract  |   June 2017
Vascular change in oxygen-induced retinopathy rat model observed using retinal optical coherence tomography angiography
Author Affiliations & Notes
  • Yongjoo Kim
    KAIST, Daejeon, Korea (the Republic of)
  • Hye kyoung Hong
    Bundang Seoul National University Hospital, Seongnam, Korea (the Republic of)
  • Jang Ryul Park
    KAIST, Daejeon, Korea (the Republic of)
  • Youjin Koh
    Bundang Seoul National University Hospital, Seongnam, Korea (the Republic of)
  • WooJhon Choi
    KAIST, Daejeon, Korea (the Republic of)
  • Se Joon Woo
    Bundang Seoul National University Hospital, Seongnam, Korea (the Republic of)
  • Kyu Hyung Park
    Bundang Seoul National University Hospital, Seongnam, Korea (the Republic of)
  • Wang-Yuhl Oh
    KAIST, Daejeon, Korea (the Republic of)
  • Footnotes
    Commercial Relationships   Yongjoo Kim, None; Hye kyoung Hong, None; Jang Ryul Park, None; Youjin Koh, None; WooJhon Choi, None; Se Joon Woo, None; Kyu Hyung Park, None; Wang-Yuhl Oh, None
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science June 2017, Vol.58, 4878. doi:
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      Yongjoo Kim, Hye kyoung Hong, Jang Ryul Park, Youjin Koh, WooJhon Choi, Se Joon Woo, Kyu Hyung Park, Wang-Yuhl Oh; Vascular change in oxygen-induced retinopathy rat model observed using retinal optical coherence tomography angiography. Invest. Ophthalmol. Vis. Sci. 2017;58(8):4878.

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

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Abstract

Purpose : Retina hypoxia is a condition that the retina lacks oxygenation due to ischemic vascular change. If the retina is in ischemic condition for a prolonged period of time, it can lead to pathologic neovascularization in the retina. To explore the pathophysiology of the ischemic retinal disease, we induced oxygen-induced retinopathy (OIR) in the rat eye, and monitored retinal microvasculature using optical coherence tomography angiography (OCTA).

Methods : Two groups of Sprague Dawley rat were prepared. The mother and pups in the OIR group were incubated in 80% oxygen chamber from one day after birth and returned to room at 12 days-old (P12), whereas the control group was remained in the room condition. A lab-built swept source OCTA system with 230 kHz A-line rate at 1050 nm was used for this study. The pups were imaged every 3 days from P15 to P24. Immunofluorescence imaging was also performed in the same eyes to compare with OCTA.

Results : The neovascular tufts sprouting above the retinal surface are observed on the intensity images in the OIR rat (Figure 1. A1~A2). The tufts can be segmented from the retina and overlaid in magenta (Figure 1. A3). The vascular development in different capillary plexus is visualized by segmenting the inner plexiform layer. The deep capillary plexus in the OIR is suppressed (Figure 1. B4) while the control groups shows distinct capillary networks (Figure 1. B1~2). The blue areas in en face vascular projection images correspond to local regions where the intensity signal is below certain threshold level due to shadowing caused by hyaloid vessels in the vitreous.

Conclusions : We observed the vascular change in the OIR rat using OCTA. In addition to neovascular tufts, quantitative analysis of retinal thickness and vascular development in different capillary plexus will be discussed.

This is an abstract that was submitted for the 2017 ARVO Annual Meeting, held in Baltimore, MD, May 7-11, 2017.

 

Figure 1. Retinal OCTA images of the OIR rats. (A1, A2) OCT intensity cross sectional images with neovascular tufts above the retinal surface. (A3) OCTA en face projection with the tufts overlaid in magenta. OCTA en face projection images of superficial and deep capillary plexus for control group (B1, B2) and for OIR group (B3, B4).

Figure 1. Retinal OCTA images of the OIR rats. (A1, A2) OCT intensity cross sectional images with neovascular tufts above the retinal surface. (A3) OCTA en face projection with the tufts overlaid in magenta. OCTA en face projection images of superficial and deep capillary plexus for control group (B1, B2) and for OIR group (B3, B4).

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