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Updated: Jul 10, 2026

Rat Mesentery Angiogenesis Assay
Published on: June 18, 2011
Peroxovanadium compounds as inhibitors of angiogenesis
C J Doillon1, R L Faure, B I Posner
1Oncology and Molecular Endocrinology, Laval University Medical Center and Laval University, Ste-Foy, Quebec, Canada. charles.doillon@crchul.ulaval.ca
Abstract:
Angiogenesis is a complex process that involves the activation of endothelial cells through the triggering of several intracellular signaling pathways including those involving tyrosine phosphorylation. In the present study, we analyzed the angiogenic properties of two phosphotyrosyl phosphatase (PTP) inhibitors that are composed of a peroxovanadium core containing different ancillary ligands. In cell monolayer and 3D culture systems examined in this study, the administration of potassium bisperoxo(1,10-phenanthroline)oxovanadate(V) [bpV(phen)] or potassium bisperoxo(pyridine-2-carboxylato)oxovanadate(V) [bpV(pic)], but not oxovanadiums, interfered markedly with endothelial cell growth, organization, and terminal differentiation. This effect was dependent upon both the compound's dose and the nature of the ancillary ligand. Rat aortic ring assay showed a significant inhibition by low dose of bpV(phen) on cell migration. In addition, a chick embryo angiogenesis assay demonstrated that bpV(phen) is a potent inhibitor of angiogenesis. Among PTP inhibitors, bpV(phen) had powerful angiostatic properties at a low concentration.
Insights
Two peroxovanadium compounds, bpV(phen) and bpV(pic), significantly inhibited endothelial cell growth and organization. bpV(phen) demonstrated potent angiostatic properties, effectively inhibiting angiogenesis in chick embryos.
Area of Science:
- Biochemistry
- Cell Biology
- Pharmacology
Background:
- Angiogenesis is crucial for development and disease, involving endothelial cell activation via signaling pathways like tyrosine phosphorylation.
- Phosphotyrosyl phosphatase (PTP) inhibitors are being explored for their therapeutic potential.
Purpose of the Study:
- To investigate the angiogenic properties of two peroxovanadium-based PTP inhibitors: potassium bisperoxo(1,10-phenanthroline)oxovanadate(V) [bpV(phen)] and potassium bisperoxo(pyridine-2-carboxylato)oxovanadate(V) [bpV(pic)].
- To assess the impact of these inhibitors on endothelial cell behavior and angiogenesis.
Main Methods:
- In vitro studies using cell monolayer and 3D culture systems to evaluate endothelial cell growth, organization, and differentiation.
- Rat aortic ring assay to assess the effect on cell migration.
- Chick embryo angiogenesis assay to determine in vivo anti-angiogenic activity.
Main Results:
- Both bpV(phen) and bpV(pic) markedly interfered with endothelial cell growth, organization, and differentiation in cell culture models.
- The observed effects were dose-dependent and influenced by the ancillary ligand.
- Low-dose bpV(phen) significantly inhibited cell migration in the rat aortic ring assay.
- bpV(phen) proved to be a potent inhibitor of angiogenesis in the chick embryo assay, exhibiting strong angiostatic properties at low concentrations.
Conclusions:
- Peroxovanadium compounds, specifically bpV(phen) and bpV(pic), possess significant anti-angiogenic and anti-endothelial cell activity.
- bpV(phen) is a potent angiostatin with therapeutic potential for conditions involving excessive angiogenesis.
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