Neovascularization in the anterior segment of the rabbit eye by experimental anterior ischemia

Graefes Arch Clin Exp Ophthalmol. 2002 Feb;240(2):144-53. doi: 10.1007/s00417-001-0420-4.

Abstract

Purpose: To investigate the effects of anterior ischemia accompanied by neither retinal nor choroidal ischemia on the anterior segment of the eye.

Methods: Both long posterior ciliary arteries in the right eye of 14 rabbits were directly cauterized with an electric coagulator. The eyes were enucleated 1, 2, 4, 7, 9 or 14 days after cauterization, then fixed with 4% paraformaldehyde. Semi-thin sections were studied by light microscopy. Several sections were stained with Griffonia simplicifolia lectin, which bound specifically to mammalian vascular endothelium. Other specimens were examined immunohistochemically for vascular endothelial growth factor (VEGF) protein. The tissue specimens of the first postoperative day were studied for expression of VEGF mRNA by in situ hybridization.

Results: Atrophy of the iris and ciliary body was seen after the second postoperative day. Corneal neovascularization appeared after 7 days. Neovascularization on the anterior surface of the iris and in the trabecular meshwork was detected after the ninth postoperative day. The proliferative tissues with newly formed vessels obstructed the iridocorneal angle 14 days after the treatment. There was no histological change in either the retina or choroid. Immunohistochemically, VEGF protein was detected in the epithelial and vascular cells of the iris on the first and fourth postoperative day. Expression of VEGF mRNA was detected in the epithelial cells of the ciliary body on the day following the treatment.

Conclusions: Anterior segment ischemia, when unaccompanied by retinal ischemia, causes neovascularization in the cornea, iris and trabecular tissue.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anterior Eye Segment / blood supply*
  • Anterior Eye Segment / pathology
  • Atrophy / pathology
  • Blotting, Western
  • Ciliary Arteries / surgery
  • Ciliary Body / blood supply
  • Ciliary Body / pathology
  • Electrocoagulation
  • Endothelial Growth Factors / genetics
  • Endothelial Growth Factors / metabolism
  • Endothelium, Vascular / metabolism
  • Endothelium, Vascular / pathology
  • Immunoenzyme Techniques
  • In Situ Hybridization
  • Iris / blood supply
  • Iris / pathology
  • Ischemia / complications*
  • Lymphokines / genetics
  • Lymphokines / metabolism
  • Neovascularization, Pathologic / etiology*
  • Neovascularization, Pathologic / pathology
  • RNA, Messenger / metabolism
  • Rabbits
  • Trabecular Meshwork / blood supply
  • Trabecular Meshwork / pathology
  • Vascular Endothelial Growth Factor A
  • Vascular Endothelial Growth Factors

Substances

  • Endothelial Growth Factors
  • Lymphokines
  • RNA, Messenger
  • Vascular Endothelial Growth Factor A
  • Vascular Endothelial Growth Factors