Intraluminal gene transfer of endothelial cell-nitric oxide synthase suppresses intimal hyperplasia of vein grafts in cholesterol-fed rabbit: A limited biological effect as a result of the loss of medial smooth muscle cells

被引:32
作者
Ohta, S [1 ]
Komori, K [1 ]
Yonemitsu, Y [1 ]
Onohara, T [1 ]
Matsumoto, T [1 ]
Sugimachi, K [1 ]
机构
[1] Kyushu Univ, Grad Sch Med Sci, Dept Surg & Sci, Higashi Ku, Fukuoka 8128582, Japan
关键词
D O I
10.1067/msy.2002.124878
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background. The intimal hyperplasia of vein grafts is a major cause of late graft failure and is more pronounced under hyperlipidemia. We previously reported that endothelial cell (ec)-type nitric oxide synthase (NOS)gene transfer inhibited graft, intimal hyperplasia under poor runoff conditions. However, little, information is available on either ecNOS gene transfer or intimal thickening under hypercholesterolemia. Methods. Using the hemagglutinating virus Japan. liposomes bovine ecNOS complentary DNA (5000 hemagglutinating activity units/mL) was transfected intraluminally to the right jugular vein, and these veins were then implanted is reversed vein grafts in an end-to-side fashion to the ipsilateral carotid artery. Results. The cyclic guanosine 3,5'-monophosphate content of the ecNOS vein significantly increased in the grafts at 4 days after gene transfer; but the levels were only 25 % greater than those found in the untreated veins. An immunohistochemical analysis at the same time suggested a large loss of medial smooth muscle cells that might have led to a reduction in the exogenous gene expression. The neointima of the ecNOS grafts was significantly reduced 4 weeks after implantation (P <.05), but the effect of ecNOS was limited to about a 30 % inhibition. This reduction was associated with a reduced population of proliferating cells and decreased macrophage accumulation in the graft wall. Conclusions. These results demonstrated that the ecNOS gene transfer suppressed intimal hyperplasia of the vein grafts under hyperlipidemic conditions. However, this effect may, be limited because of the smooth muscle cell loss related to the use of an intraluminal delivery, methods. These data lead to speculation that the outcome of ecNOS gene transfer could be improved using different methods of gene delivery.
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页码:644 / 653
页数:10
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