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[Inhibition of corneal neovascularization by a new analog of fungal product].

Abstract
The anti-angiogenic activity if FR 118487, a new synthetic analogue of Scolecobasidium arenarium products, was examined in corneas of Japanese white rabbits. We studied locally administered FR 118487 with hydron pellets in two models; corneal neovascularization after implantation of a CuCl2 pellet (CuCl2-induced model) and a Wistar rat's cornea (keratoplasty model) into a rabbit cornea. In the CuCl2-induced model, maximum length of neovascularization was 0.08 +/- 0.10 (mean +/- standard deviation) mm with FR 118487 (control 2.84 +/- 0.13 mm) at 1 week after the implantation. In the keratoplasty model, maximum length of neovascularization was 0.05 +/- 0.05 mm with FR 118487 (control 3.33 +/- 0.18 mm) at 2 weeks after the implantation. In both models, FR 118487 had a significant (p < 0.01) effect on inhibition of corneal neovascularization.
AuthorsS Nii, T Idei, H Terano, Y Mashima
JournalNippon Ganka Gakkai zasshi (Nippon Ganka Gakkai Zasshi) Vol. 101 Issue 6 Pg. 465-9 (Jun 1997) ISSN: 0029-0203 [Print] Japan
PMID9209132 (Publication Type: English Abstract, Journal Article)
Chemical References
  • FR 118487
  • Spiro Compounds
  • Copper
  • cuprous chloride
Topics
  • Animals
  • Copper
  • Corneal Neovascularization (chemically induced, drug therapy)
  • Corneal Transplantation (adverse effects)
  • Disease Models, Animal
  • Female
  • Fungi
  • Rabbits
  • Rats
  • Rats, Wistar
  • Spiro Compounds (therapeutic use)

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