Title of article :
Comparison of Gene Delivery Techniques for Therapeutic Angiogenesis: Ultrasound-Mediated Destruction of Carrier Microbubbles Versus Direct Intramuscular Injection
Author/Authors :
Kobulnik، نويسنده , , Jeremy and Kuliszewski، نويسنده , , Michael A. and Stewart، نويسنده , , Duncan J. and Lindner، نويسنده , , Jonathan R. and Leong-Poi، نويسنده , , Howard، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2009
Pages :
8
From page :
1735
To page :
1742
Abstract :
Objectives tudy was designed to compare the efficacy of angiogenic gene delivery by ultrasound-mediated (UM) destruction of intravenous carrier microbubbles to direct intramuscular (IM) injections. ound t trials of gene therapy for angiogenesis remain limited by suboptimal, invasive delivery techniques. s imb ischemia was produced by iliac artery ligation in 99 rats. In 32 rats, UM delivery of green fluorescent protein (GFP)/vascular endothelial growth factor-165 (VEGF165) plasmid deoxyribonucleic acid was performed. Thirty-five animals received IM injections of VEGF165/GFP plasmid. Remaining rats received no treatment. Before delivery (day 14 after ligation) and at days 17, 21, and 28 and week 8 after ligation, microvascular blood volume and microvascular blood flow to the proximal hind limbs were assessed by contrast-enhanced ultrasound (n = 8 per group). Total transfection was assessed by reverse transcriptase–polymerase chain reaction, and localization of transfection was determined by immunohistochemistry. s 28, both IM and UM delivery of VEGF165 produced significant increases in microvascular blood volume and microvascular blood flow. Whereas increases in microvascular blood volume were similar between treatment groups, microvascular blood flow was greater (p < 0.005) in UM-treated animals as compared with IM-treated animals, persisting to week 8. The VEGF165/GFP messenger ribonucleic acid expression was greater (p < 0.05) for IM-treated animals. A strong GFP signal was detected for both groups and was localized to focal perivascular regions and myocytes around injection sites for IM and to the vascular endothelium of arterioles/capillaries in a wider distribution for UM delivery. sions e lower transfection levels, UM delivery of VEGF165 is as effective as IM injections. The UM delivery results in directed vascular transfection over a wider distribution, which may account for the more efficient angiogenesis.
Keywords :
Angiogenesis , Gene Therapy , chronic ischemia
Journal title :
JACC (Journal of the American College of Cardiology)
Serial Year :
2009
Journal title :
JACC (Journal of the American College of Cardiology)
Record number :
1745918
Link To Document :
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