Interaction between iNOS and COX-2 in hypoxia-induced retinal neovascularization in mice

Arch Med Res. 2007 Nov;38(8):807-15. doi: 10.1016/j.arcmed.2007.05.003. Epub 2007 Aug 20.

Abstract

Background: Upregulation of cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS) has been reported in hypoxia-induced retinal angiogenesis. The aim of our study was to evaluate the possible interaction between the COX and NOS pathways and the effect of this interaction on matrix metalloproteinases 2 (MMP-2) and vascular endothelial growth factor (VEGF) expression and on retinal angiogenesis.

Methods: In this study, the effect of COX-2 or iNOS inhibition on retinal angiogenesis was examined by histopathology. Expression of iNOS, COX-2, MMP-2, and VEGF in the retinas of experimental animals was analyzed using immunohistochemistry, real-time PCR, and Western blotting technologies.

Results: Inhibition of COX-2 or iNOS attenuated retinal neovascularization and decreased VEGF and MMP-2 expression. An interaction was found between COX-2 and iNOS expression: the iNOS inhibition decreased COX-2 expression and vice versa.

Conclusions: Our data showed a prominent role of COX-2 and iNOS in hypoxia-induced retinal angiogenesis. The interaction between COX-2 and iNOS is likely to produce a cooperative effect on retinal angiogenesis. The changes of MMP-2 and VEGF expression may play a role in the process of retinal neovascularization.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Blotting, Western
  • Cell Hypoxia / drug effects
  • Cell Hypoxia / physiology*
  • Cyclooxygenase 2 / metabolism*
  • Cyclooxygenase Inhibitors / pharmacology
  • Female
  • Immunohistochemistry
  • Matrix Metalloproteinase 2 / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Nitric Oxide Synthase Type II / antagonists & inhibitors
  • Nitric Oxide Synthase Type II / metabolism*
  • Polymerase Chain Reaction
  • Pregnancy
  • RNA, Messenger / metabolism
  • Random Allocation
  • Retinal Neovascularization / etiology*
  • Retinal Neovascularization / pathology
  • Retinal Neovascularization / prevention & control*
  • Up-Regulation
  • Vascular Endothelial Growth Factor A / genetics
  • Vascular Endothelial Growth Factor A / metabolism

Substances

  • Cyclooxygenase Inhibitors
  • RNA, Messenger
  • Vascular Endothelial Growth Factor A
  • Nitric Oxide Synthase Type II
  • Ptgs2 protein, mouse
  • Cyclooxygenase 2
  • Matrix Metalloproteinase 2