April 2014
Volume 55, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2014
Experimental model for development of proliferative retinopathy after injection of intravitreal VEGF-A 165 in rabbits
Author Affiliations & Notes
  • Emmerson Badaro
    Retina and Vitreous, Federal University of Sao Paulo, Sao Paulo, Brazil
  • Eduardo Novais
    Retina and Vitreous, Federal University of Sao Paulo, Sao Paulo, Brazil
  • Muller Urias
    Retina and Vitreous, Federal University of Sao Paulo, Sao Paulo, Brazil
  • Paulo Augusto Mello Filho
    Retina and Vitreous, Federal University of Sao Paulo, Sao Paulo, Brazil
  • Eduardo Rodrigues
    Retina and Vitreous, Federal University of Sao Paulo, Sao Paulo, Brazil
  • Michel Farah
    Retina and Vitreous, Federal University of Sao Paulo, Sao Paulo, Brazil
  • Footnotes
    Commercial Relationships Emmerson Badaro, None; Eduardo Novais, None; Muller Urias, None; Paulo Augusto Mello Filho, None; Eduardo Rodrigues, None; Michel Farah, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science April 2014, Vol.55, 4909. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      Emmerson Badaro, Eduardo Novais, Muller Urias, Paulo Augusto Mello Filho, Eduardo Rodrigues, Michel Farah; Experimental model for development of proliferative retinopathy after injection of intravitreal VEGF-A 165 in rabbits. Invest. Ophthalmol. Vis. Sci. 2014;55(13):4909.

      Download citation file:


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

      ×
  • Supplements
Abstract
 
Purpose
 

To develop a proliferative retinopathy experimental model by intravitreal injection of VEGF in pigmented rabbits.

 
Methods
 

A prospective, controlled, comparative, interventional study. Six pigmented rabbits were submitted to intravitreal injection of VEGF-165 in their right eye. Left eye was used as control. In group 1, four rabbits received a 10μg injection and, in group 2, two received 20μg. At baseline and week 1, 2 and 5 all were analyzed with anterior biomicroscopy, retinography, fluoresceinic angiography and OCT images. In the fifth week after the injection the rabbits were euthanized and the eyes were enucleated and submitted to a histological evaluation. The ocular examination was analyzed according to the anatomy of the vessels and evaluated for: disc hyperemia, vascular dilatation and tortuosity, vitreal or retinal leakage, formation of neovascular membrane, vascular narrowing, disc pallor, abnormal vascular pattern, retinal distortion and elevation or capillary non-perfusion.

 
Results
 

Seven days after the intravitreal VEGF-165 injection, all rabbits developed intense neovascularization of the retina and anterior segment. The neovascularization of the posterior pole was similar in both groups, and the anterior segment was more important in group 2. During week 1 and 2, the neovascularization was maintained with minor decrease of conjunctival hyperemia in both groups. At week 5 there was a partial regression of the neovascularization of posterior pole, more prominent in group 1 than group 2, with persistent anterior neovascularization in both groups. After a five-week period, ocular histopathological evaluation showed intense neovascularization in group 2.

 
Conclusions
 

The pilot study for model of neovascularization through intravitreal VEGF-165 injection in pigmented rabbits show that both doses of 10 and 20µg were successful to develop retina and anterior segment vascular growth, and therefore can be used for evaluation of drugs efficacy in future studies.

 
 
Figure 1 A) Colored fundus Retinography and C) Fluorescein Angiography showing intense neovascularization seven days after the VEGF-165 intravitreous injection B) Colored fundus Retinography and C) Fluorescein Angiography showing normal findings
 
Figure 1 A) Colored fundus Retinography and C) Fluorescein Angiography showing intense neovascularization seven days after the VEGF-165 intravitreous injection B) Colored fundus Retinography and C) Fluorescein Angiography showing normal findings
 
 
Figure 2 A)Spectral-Domain OCT showing normal retinal and choroidal layers B)Spectral-Domain OCT showing vitreous opacities and disorganization of the retinal layers.
 
Figure 2 A)Spectral-Domain OCT showing normal retinal and choroidal layers B)Spectral-Domain OCT showing vitreous opacities and disorganization of the retinal layers.
 
Keywords: 748 vascular endothelial growth factor • 700 retinal neovascularization  
×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×