Effect of light on oxygen-induced retinopathy in the mouse

Invest Ophthalmol Vis Sci. 1994 Jan;35(1):112-9.

Abstract

Purpose: To examine the effect lf light on retinal neovascularization and vasculogenesis in a reproducible and quantifiable model of oxygen-induced proliferative retinopathy in the mouse.

Methods: C57Bl/6J mice were reared in room air, 68% oxygen, or 75% oxygen and were exposed to darkness, low cyclical light (200-350 lux), or high-intensity continuous light (3000-4500 lux). The entire retinal vascular pattern was visualized in fluorescein-dextran perfused flat-mount preparations. Proliferative retinopathy was quantified by counting neovascular nuclei in 6 microns cross-sections of whole eyes.

Results: Light exposure did not exacerbate the proliferative retinopathy that was seen after 68% oxygen exposure, which induced a meager proliferative response, nor after 75% oxygen exposure, which induced an exuberant proliferative response. In room air, retinas from all three illumination groups had normal vascular patterns.

Conclusions: In this model of oxygen-induced retinopathy, under the conditions tested, light neither exacerbated the hyperoxia-induced neovascularization nor affected normal retinal vascular development.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Dark Adaptation
  • Dextrans
  • Disease Models, Animal
  • Fluorescein Angiography
  • Fluoresceins
  • Fundus Oculi
  • Humans
  • Infant, Newborn
  • Light*
  • Mice
  • Mice, Inbred C57BL
  • Perfusion
  • Random Allocation
  • Retinal Vessels / pathology
  • Retinal Vessels / radiation effects*
  • Retinopathy of Prematurity / pathology*
  • Retinopathy of Prematurity / physiopathology

Substances

  • Dextrans
  • Fluoresceins
  • fluorescein-dextran