Matsuda T, Motomura N, Oka T
Department of Bioengineering, National Cardiovascular Center Research Institute, Osaka, Japan.
ASAIO J. 1993 Jul-Sep;39(3):M512-7.
We studied a pharmacologic approach using a potent peptidyl antiproliferative agent, angiopeptin, to prevent the myointimal hyperplasia that occurs as a diseased vessel is replaced with an artificial graft or treated by an intravascular device. In vitro cell culture studies showed that the proliferative potential of smooth muscle cells was dose dependently reduced, whereas the migratory response was reduced to a lesser degree. In a well defined injured rat artery model, in which a denuded aorta was prepared by collagenase treatment, followed by isotransplantation, a remarkable suppressive effect of angiopeptin on myointimal hyperplasia was observed with daily subcutaneous injection. Local sustained release from a biodegradable polymeric gel coated on an injured vessel was also effective in the prevention of myointimal hyperplasia. Slightly retarded endothelial regeneration was noticed. The potential application to small caliber artificial grafts is discussed.
我们研究了一种药理学方法,即使用一种强效肽类抗增殖剂血管肽,以预防在病变血管被人工移植物替代或通过血管内装置治疗时发生的肌内膜增生。体外细胞培养研究表明,平滑肌细胞的增殖潜能呈剂量依赖性降低,而迁移反应的降低程度较小。在一个明确的大鼠动脉损伤模型中,通过胶原酶处理制备去内皮主动脉,然后进行同基因移植,每日皮下注射血管肽可观察到其对肌内膜增生有显著的抑制作用。涂覆在损伤血管上的可生物降解聚合物凝胶的局部持续释放对预防肌内膜增生也有效。注意到内皮再生略有延迟。文中讨论了其在小口径人工移植物中的潜在应用。