Dose-dependent neovascularization-promoting effect of adenovirus vector CI-1023 in a rat hindlimb ischaemic model

Basic Clin Pharmacol Toxicol. 2004 Aug;95(2):76-80. doi: 10.1111/j.1742-7843.2004.950206.x.

Abstract

CI-1023 (AdGVVEGF121.10) is a replication-deficient adenovirus vector (complete E1a-, partial E1b-, partial E3-) delivering human vascular endothelial growth factor-121 gene. Previous studies from this group have established that CI-1023 can successfully transfer human vascular endothelial growth factor-121 gene resulting in local tissue expression of vascular endothelial growth factor protein. The purpose of this study was to evaluate neovascularization-promoting potency and efficacy of CI-1023 in a wide dose range. In a rat hindlimb ischaemic model, we measured neovascularization-promoting effect of CI-1023 using three end-points: post mortem angiography, immuno-histochemistry and Laser Doppler scanning of tissue blood perfusion. Neovascularization-promoting activity of CI-1023 over the dose range of 4 x 10(6) pu-4 x 10(10) pu was evaluated. Our data demonstrated an obvious dose-dependent effect between 4 x 10(6) pu-4 x 10(8) pu. The neovascularizing effect is somewhat plateaued at the levels between 4 x 10(8) pu and 4 x 10(10) pu. We conclude CI-1023 is a potent neovascularization-promoting compound, with a dose-dependent effect between 4 x 10(6) pu-4 x 10(8) pu in the rat hindlimb ischaemic model.

Publication types

  • Comparative Study

MeSH terms

  • Angiogenic Proteins / administration & dosage
  • Angiogenic Proteins / pharmacology*
  • Angiogenic Proteins / therapeutic use
  • Angiography / methods
  • Animals
  • Disease Models, Animal
  • Dose-Response Relationship, Drug*
  • Drug Evaluation, Preclinical / methods
  • Genetic Vectors / administration & dosage
  • Genetic Vectors / chemistry
  • Genetic Vectors / pharmacology
  • Hindlimb / blood supply
  • Hindlimb / drug effects*
  • Lymphokines / administration & dosage
  • Lymphokines / pharmacology*
  • Lymphokines / therapeutic use
  • Male
  • Neovascularization, Physiologic / drug effects*
  • Neovascularization, Physiologic / physiology
  • Perfusion
  • Rats
  • Rats, Sprague-Dawley
  • Time Factors
  • Vascular Endothelial Growth Factors / genetics
  • Vascular Endothelial Growth Factors / metabolism

Substances

  • AdGVVEGF121.10
  • Angiogenic Proteins
  • Lymphokines
  • Vascular Endothelial Growth Factors