Suppression of choroidal neovascularization by inhibiting angiotensin-converting enzyme: minimal role of bradykinin

Invest Ophthalmol Vis Sci. 2007 May;48(5):2321-6. doi: 10.1167/iovs.06-1296.

Abstract

Purpose: Angiotensin-converting enzyme (ACE), also known as kininase II, functions not only to convert angiotensin I to angiotensin II, but also to cleave bradykinin into inactive fragments. Thus, ACE inhibition causes the tissue accumulation of bradykinin, exerting either of two opposite effects: anti- or proangiogenic. The purpose of the present study was to investigate the role of bradykinin in the development of choroidal neovascularization (CNV), with or without ACE inhibition.

Methods: Laser photocoagulation was used to induce CNV in wild-type C57BL/6J mice and angiotensin II type 1 receptor (AT1-R)-deficient mice. Wild-type mice were pretreated with the ACE inhibitor imidapril, with or without the bradykinin B2 receptor (B2-R) antagonist icatibant daily for 6 days before photocoagulation, and the treatment was continued daily until the end of the study. CNV response was analyzed by volumetric measurements using confocal microscopy 1 week after laser injury. The mRNA and protein levels of vascular endothelial growth factor (VEGF), intercellular adhesion molecule (ICAM)-1, and monocyte chemotactic protein (MCP)-1 in the retinal pigment epithelium-choroid complex were examined by RT-PCR and ELISA, respectively.

Results: ACE inhibition led to significant suppression of CNV development to the level seen in AT1-R-deficient mice. B2-R blockade together with high-dose but not low-dose ACE inhibition resulted in more potent suppression of CNV than did ACE inhibition alone. B2-R blockade alone exhibited little or no effect on CNV. VEGF, ICAM-1, and MCP-1 levels, elevated by CNV induction, were significantly suppressed by ACE inhibition. VEGF but not ICAM-1 or MCP-1 levels were further attenuated by B2-R blockade with ACE inhibition.

Conclusions: These results suggest a limited contribution of the kallikrein-kinin system to the pathogenesis of CNV, in which the renin-angiotensin system plays more essential roles for facilitating angiogenesis. The present study indicates the possibility of ACE inhibition as a novel therapeutic strategy to inhibit CNV.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiotensin-Converting Enzyme Inhibitors / pharmacology*
  • Animals
  • Bradykinin / analogs & derivatives
  • Bradykinin / pharmacology
  • Bradykinin / physiology*
  • Bradykinin B2 Receptor Antagonists
  • Chemokine CCL2 / genetics
  • Chemokine CCL2 / metabolism
  • Choroid / metabolism
  • Choroidal Neovascularization / metabolism
  • Choroidal Neovascularization / pathology
  • Choroidal Neovascularization / prevention & control*
  • Disease Models, Animal
  • Enzyme-Linked Immunosorbent Assay
  • Imidazolidines / pharmacology*
  • Intercellular Adhesion Molecule-1 / genetics
  • Intercellular Adhesion Molecule-1 / metabolism
  • Kallikrein-Kinin System / physiology
  • Laser Coagulation
  • Mice
  • Mice, Inbred C57BL
  • Microscopy, Confocal
  • Peptidyl-Dipeptidase A / physiology*
  • Pigment Epithelium of Eye / metabolism
  • RNA, Messenger / metabolism
  • Receptor, Angiotensin, Type 1 / deficiency
  • Reverse Transcriptase Polymerase Chain Reaction
  • Vascular Endothelial Growth Factor A / genetics
  • Vascular Endothelial Growth Factor A / metabolism

Substances

  • Angiotensin-Converting Enzyme Inhibitors
  • Bradykinin B2 Receptor Antagonists
  • Ccl2 protein, rat
  • Chemokine CCL2
  • Imidazolidines
  • RNA, Messenger
  • Receptor, Angiotensin, Type 1
  • Vascular Endothelial Growth Factor A
  • vascular endothelial growth factor A, rat
  • Intercellular Adhesion Molecule-1
  • icatibant
  • imidapril
  • Peptidyl-Dipeptidase A
  • Bradykinin