4.7 Article

Sustained Improvement in Perfusion and Flow Reserve After Temporally Separated Delivery of Vascular Endothelial Growth Factor and Angiopoietin-1 Plasmid Deoxyribonucleic Acid

Journal

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
Volume 59, Issue 14, Pages 1320-1328

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jacc.2011.12.025

Keywords

angiogenesis; cationic microbubbles; chronic ischemia; gene therapy; ultrasound

Funding

  1. Canadian Institutes of Health Research, Ottawa, Ontario, Canada [MOP 62763]
  2. Canadian Foundation for Innovation, Ottawa, Ontario, Canada
  3. Heart and Stroke Foundation of Ontario, Ottawa, Ontario, Canada
  4. Ministry of Research and Innovation, Ontario, Canada

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Objectives The aim of this study was to compare temporally separated vascular endothelial growth factor (VEGF) and angiopoietin (Ang)-1 delivery with concomitant delivery or single VEGF delivery, for therapeutic angiogenesis in chronic ischemia. Background Single gene delivery of VEGF results in immature neovessels that ultimately regress. Endogenously, VEGF acts early to initiate angiogenesis, whereas Ang-1 acts later to induce vessel maturation. Timing VEGF and Ang-1 gene delivery to mimic endogenous angiogenesis might be more effective for sustained neovascularization. Methods Unilateral hindlimb ischemia was induced in 170 rats. Ultrasound-mediated gene delivery was performed with cationic microbubbles and plasmid deoxyribonucleic acid. Groups included VEGF at 2 weeks, VEGF/Ang-1 at 2 weeks, VEGF at 2 weeks with Ang-1 at 4 weeks, and untreated control subjects. At 2, 4, and 8 weeks after ligation, blood flow and flow reserve (FR) were assessed by contrast-enhanced ultrasound. Vascular density, organization, and supporting cell coverage were assessed by fluorescent microangiography and immunohistochemistry. Results In untreated control subjects, blood flow, FR, and vessel density remained reduced. The VEGF delivery improved flow and vessel density at 4 weeks; however, FR remained low, supporting cell coverage was poor, and flow and vessel density regressed by 8 weeks. The VEGF/Ang-1 co-delivery marginally increased flow and vessel density; however, FR and supporting cell coverage improved. After temporally separated VEGF and Ang-1 delivery, blood flow, vessel density, and FR increased and were sustained, with improved pericyte coverage at 8 weeks. Conclusions In conclusion, temporally separated VEGF and Ang-1 gene therapy results in sustained and functional neovascularization. (J Am Coll Cardiol 2012;59:1320-8) (C) 2012 by the American College of Cardiology Foundation

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