Kipshidze Nicholas N, Iversen Patrick, Kim Han-Soo, Yiazdi Hamid, Dangas George, Seaborn Rufus, New Gishel, Tio Fermin, Waksman Ron, Mehran Roxana, Tsapenko Mykola, Stone Gregg W, Roubin Gary S, Iyer Sriram, Leon Martin B, Moses Jeffrey W
Lenox Hill Heart and Vascular Institute and Cardiovascular Research Foundation, New York, New York 10021, USA.
Catheter Cardiovasc Interv. 2004 Apr;61(4):518-27. doi: 10.1002/ccd.20007.
An advanced six-ring morpholino backbone c-myc antisense (AVI-4126) was shown to inhibit c-myc expression and intimal hyperplasia after local catheter delivery in a porcine balloon injury model. The purpose of this study was to investigate the effects of an AVI-4126-eluting phosphorylcholine-coated (PC) stent on c-myc expression restenosis and vascular healing after stent implantation in porcine coronary arteries. PC stents were loaded with AVI-4126 using soak trap. Nine pigs underwent AVI-4126 PC coronary stent implantation (two stents/animal). Two to six hours postprocedure, three pigs were sacrificed and stented segments were analyzed by Western blot for c-myc expression. In chronic experiments, six pigs (12 stent sites) were sacrificed at 28 days following intervention and vessels were perfusion-fixed. High-performance liquid chromatography analysis of plasma samples showed minimal presence of the antisense. Western blot analysis of the stented vessels demonstrated inhibition of c-myc expression at 2 and 6 hr after procedure. Quantitative histologic morphometry showed that the neointimal area was significantly reduced (by 40%) in the antisense-coated group compared with control (2.3 +/- 0.7 vs. 3.9 +/- 0.8 mm(2), respectively; P = 0.0077). Immunostaining and electron microscopy demonstrated complete endothelialization, without fibrin deposition, thrombosis, or necrosis in all implanted stents. In the porcine coronary model, an advanced c-myc-eluting PC stent blocked c-myc expression and significantly inhibited myointimal hyperplasia and allowed complete reendothelialization and healing response.
在猪球囊损伤模型中,一种先进的六环吗啉代骨架c-myc反义寡核苷酸(AVI-4126)经局部导管给药后可抑制c-myc表达和内膜增生。本研究旨在探讨载有AVI-4126的磷酸胆碱涂层(PC)支架对猪冠状动脉支架植入术后c-myc表达、再狭窄及血管愈合的影响。采用浸泡捕获法将AVI-4126加载到PC支架上。9头猪接受了AVI-4126 PC冠状动脉支架植入术(每头动物植入2个支架)。术后2至6小时,处死3头猪,通过蛋白质免疫印迹法分析支架段的c-myc表达。在慢性实验中,干预后28天处死6头猪(12个支架植入部位),对血管进行灌注固定。血浆样本的高效液相色谱分析显示反义寡核苷酸的含量极低。对植入支架的血管进行蛋白质免疫印迹分析显示,术后2小时和6小时c-myc表达受到抑制。定量组织形态学分析表明,与对照组相比,反义寡核苷酸涂层组的新生内膜面积显著减少(减少40%)(分别为2.3±0.7 vs. 3.9±0.8 mm²;P = 0.0077)。免疫染色和电子显微镜检查显示,所有植入的支架均实现了完全内皮化,无纤维蛋白沉积、血栓形成或坏死。在猪冠状动脉模型中,一种先进的c-myc洗脱PC支架可阻断c-myc表达,显著抑制肌内膜增生,并实现完全再内皮化和愈合反应。