Adenovirus-mediated gene transfer of superoxide dismutase and catalase decreases restenosis after balloon angioplasty

被引:30
作者
Durand, E [1 ]
Zen, AA [1 ]
Addad, F [1 ]
Brasselet, C [1 ]
Caligiuri, G [1 ]
Vinchon, F [1 ]
Lemarchand, P [1 ]
Desnos, M [1 ]
Bruneval, P [1 ]
Lafont, A [1 ]
机构
[1] Univ Paris 05, European Georges Pompidou Hosp, AP HP,INSERM E00 16, Fac Med Paris 5, Paris, France
关键词
restenosis; redox signaling; gene therapy; endothelial function; extracellular matrix;
D O I
10.1159/000085658
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Background: Reactive oxygen species (ROS) production increases after injury and potentially contributes to restenosis after angioplasty. We therefore evaluated the effect of adenovirus-mediated gene transfer ( Ad) of superoxide dismutase ( SOD) and catalase ( CAT) on ROS production and restenosis after balloon angioplasty. Methods: O-2(-) and H2O2 production was quantified in cultured cells after incubation with either LPS or CuSO4. Angioplasty and gene transfer were performed in rabbit atherosclerotic iliac arteries. One artery was injected with AdSOD and AdCAT, while the contralateral artery was injected with an adenovirus carrying no transgene, and served as control. Results: ROS production was significantly decreased after adenovirus-mediated gene transfer of SOD and CAT as compared with control. Treated arteries showed less restenosis (32 +/- 27 vs. 63 +/- 19%, p = 0.003) and less constrictive remodeling (1.2 +/- 0.3 vs. 0.9 +/- 0.2, p = 0.02) than control arteries. Arteries injected with AdSOD and AdCAT showed better vasoreactivity to acetylcholine (11 +/- 4 vs. -1 +/- 6%, p < 0.05), lower collagen density (43 +/- 16 vs. 53 +/- 23%, p = 0.03), and lower inflammatory cell infiltration ( 22 8 6 vs. 36 +/- 11%, p = 0.04) than control arteries. Conclusions: Our data suggest that adenovirus-mediated gene transfer of SOD and CAT reduced oxidative stress, restenosis, collagen accumulation, and inflammation and improved endothelial function after angioplasty. Copyright (C) 2005 S. Karger AG, Basel.
引用
收藏
页码:255 / 265
页数:11
相关论文
共 45 条
[21]   Adenovirus-mediated extracellular superoxide dismutase gene therapy reduces neointima formation in balloon-denuded rabbit aorta [J].
Laukkanen, MO ;
Kivelä, A ;
Rissanen, T ;
Rutanen, J ;
Karkkainen, MK ;
Leppanen, O ;
Bräsen, JH ;
Yla-Herttuala, S .
CIRCULATION, 2002, 106 (15) :1999-2003
[22]  
Li PF, 1997, CIRCULATION, V96, P3602
[23]   GENETIC-EVIDENCE FOR A COMMON PATHWAY MEDIATING OXIDATIVE STRESS, INFLAMMATORY GENE INDUCTION, AND AORTIC FATTY STREAK FORMATION IN MICE [J].
LIAO, F ;
ANDALIBI, A ;
QIAO, JH ;
ALLAYEE, H ;
FOGELMAN, AM ;
LUSIS, AJ .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (02) :877-884
[24]   Oxidation of extracellular matrix modulates susceptibility to degradation by the mesangial matrix metalloproteinase-2 [J].
Mattana, J ;
Margiloff, L ;
Chaplia, L .
FREE RADICAL BIOLOGY AND MEDICINE, 1999, 27 (3-4) :315-321
[25]   Superoxide production in vascular smooth muscle contributes to oxidative stress and impaired relaxation in atherosclerosis [J].
Miller, FJ ;
Gutterman, DD ;
Rios, CD ;
Heistad, DD ;
Davidson, BL .
CIRCULATION RESEARCH, 1998, 82 (12) :1298-1305
[26]   Adenovirus-mediated gene transfer into normal rabbit arteries results in prolonged vascular cell activation, inflammation, and neointimal hyperplasia [J].
Newman, KD ;
Dunn, PF ;
Owens, JW ;
Schulick, AH ;
Virmani, R ;
Sukhova, G ;
Libby, P ;
Dichek, DA .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 96 (06) :2955-2965
[27]   CYPZE1-mediated oxidative stress induces collagen type I expression in rat hepatic stellate cells [J].
Nieto, N ;
Friedman, SL ;
Greenwel, P ;
Cederbaum, AI .
HEPATOLOGY, 1999, 30 (04) :987-996
[28]   COMBINATION OF VITAMIN-C AND VITAMIN-E ALTERS THE RESPONSE TO CORONARY BALLOON INJURY IN THE PIG [J].
NUNES, GL ;
SGOUTAS, DS ;
REDDEN, RA ;
SIGMAN, SR ;
GRAVANIS, MB ;
KING, SB ;
BERK, BC .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1995, 15 (01) :156-165
[29]  
Pollman MJ, 1999, CIRC RES, V84, P113
[30]  
RAO GN, 1992, CIRC RES, V18, P775