Adenoviral-mediated transfer of vascular endothelial growth factor 121 cDNA enhances myocardial perfusion and exercise performance in the nonischemic state. Academic Article Article uri icon

Overview

MeSH

  • Animals
  • Coronary Circulation
  • Endothelial Cells
  • Endothelium, Vascular
  • Genetic Vectors
  • Heart Septum
  • Heart Ventricles
  • Male
  • Models, Animal
  • Models, Cardiovascular
  • Rabbits
  • Rats
  • Rats, Sprague-Dawley
  • Time Factors

MeSH Major

  • Adenoviridae
  • DNA, Complementary
  • Exercise Tolerance
  • Gene Transfer Techniques
  • Genetic Therapy
  • Myocardial Ischemia
  • Myocardial Reperfusion
  • Vascular Endothelial Growth Factor A

abstract

  • Angiogenic gene therapy has been demonstrated to enhance perfusion to ischemic tissues, but it is unknown whether the administration of angiogenic growth factors will increase blood flow to nonischemic tissues. This study investigates whether enhanced myocardial perfusion can be mediated by adenovirus-mediated transfer of vascular endothelial growth factor 121 cDNA to nonischemic myocardium. New Zealand White rabbits received adenovirus (5 x 10(10) particle units) encoding for vascular endothelial growth factor 121 (n = 14) or a control vector without a transgene (n = 13) or saline solution (n = 9) via direct myocardial injection. Fluorescent microsphere perfusion studies and histologic analyses were performed 4 weeks later. In a parallel study, exercise treadmill testing was performed to assess the functional effects of this therapy in Sprague-Dawley rats. Microsphere assessment of myocardial perfusion in rabbits 4 weeks after adenovirus-encoding vascular endothelial growth factor administration was greater than that for rats injected with control vector without a transgene or saline solution (3.2 +/- 0.5 vs 2.7 +/- 0.7 and 2.4 +/- 0.4, respectively; P <.03). The endothelial cell count per high power field was increased in animals injected with adenovirus-encoding vascular endothelial growth factor versus animals injected with control vector without a transgene or saline solution (147 +/- 27 vs 123 +/- 14 and 125 +/- 16 cells, respectively), although this did not reach statistical significance (P =.12). Rats treated with adenovirus-encoding vascular endothelial growth factor also demonstrated prolonged exercise tolerance compared with rats injected with control vector without a transgene or saline solution (exhaustion time: 26 +/- 5 minutes vs 19 +/- 2 minutes and 20 +/- 3 minutes, respectively; P =.006). Adenovirus encoding-mediated transfer of vascular endothelial growth factor 121 induces an enhancement in regional perfusion in nonischemic myocardium that corresponds to changes in exercise tolerance. Adenovirus-encoding vascular endothelial growth factor therapy may be useful for inducing angiogenesis in the nonischemic state, such as for prophylactic therapy of early coronary artery disease.

publication date

  • February 2004

has subject area

  • Adenoviridae
  • Animals
  • Coronary Circulation
  • DNA, Complementary
  • Endothelial Cells
  • Endothelium, Vascular
  • Exercise Tolerance
  • Gene Transfer Techniques
  • Genetic Therapy
  • Genetic Vectors
  • Heart Septum
  • Heart Ventricles
  • Male
  • Models, Animal
  • Models, Cardiovascular
  • Myocardial Ischemia
  • Myocardial Reperfusion
  • Rabbits
  • Rats
  • Rats, Sprague-Dawley
  • Time Factors
  • Vascular Endothelial Growth Factor A

Research

keywords

  • Comparative Study
  • Journal Article

Identity

Language

  • eng

Digital Object Identifier (DOI)

  • 10.1016/j.jtcvs.2003.06.015

PubMed ID

  • 14762365

Additional Document Info

start page

  • 535

end page

  • 540

volume

  • 127

number

  • 2