Antioxidant vitamins increase the collagen content and reduce MMP-1 in a porcine model of atherosclerosis:: implications for plaque stabilization

被引:50
作者
Orbe, J [1 ]
Rodríguez, JA [1 ]
Arias, R [1 ]
Belzunce, M [1 ]
Nespereira, B [1 ]
Pérez-Ilzarbe, M [1 ]
Roncal, C [1 ]
Páramo, JA [1 ]
机构
[1] Univ Navarra, Sch Med, Div Cardiovasc Pathophysiol, Atherosclerosis Res Lab, E-31008 Pamplona, Spain
关键词
antioxidant vitamins; hypercholesterolemia; atherosclerosis; collagen; metalloproteinase-1;
D O I
10.1016/S0021-9150(02)00392-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Degradation of extracellular matrix, particularly interstitial collagen, promotes plaque instability and contributes to restenosis after vascular injury. We have explored the effects of vitamins C and E on the collagen content and metalloproteinase-1 (MMP-1) expression after angioplasty in hypercholesterolemic pigs. Iliac angioplasty was performed on 18 minipigs divided into three diet groups: a normal-cholesterol (NC), a high-cholesterol (HC) and a high-cholesterol plus vitamins C+E (HCV). Four weeks later, after sacrifice, the vascular collagen content and MMP-1 protein expression, along with the plasma caseinolytic activity and lipid peroxidation, were measured. MMP-1 was also determined in arterial rings stimulated with native low-density lipoproteins (LDL) isolated from experimental groups. Cholesterol-rich diet augmented plasma lipid peroxidation (P < 0.05), reduced the collagen content and increased vascular MMP-1 expression after injury (P < 0.05). Enhanced caseinolytic activity (identified as MMP-1) was also observed in HC plasma samples and in supernatants from arterial rings incubated with HC-LDL. Vitamins C and E markedly increased neointimal collagen content (P < 0.01), reduced the hypercholesterolernia-induced changes in vascular MMP-1 (P < 0.05) and diminished plasma and ex vivo caseinolytic activity. Vitamins C and E may help stabilize atherosclerotic plaque after angioplasty and favor vascular remodeling by increasing collagen content and reducing vascular MMP-1 expression in porcine hypercholesterolemia. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:45 / 53
页数:9
相关论文
共 35 条
[1]   Lipid lowering by diet reduces matrix metalloproteinase activity and increases collagen content of rabbit atheroma - A potential mechanism of lesion stabilization [J].
Aikawa, M ;
Rabkin, E ;
Okada, Y ;
Voglic, SJ ;
Clinton, SK ;
Brinckerhoff, CE ;
Sukhova, GK ;
Libby, P .
CIRCULATION, 1998, 97 (24) :2433-2444
[2]   Inhibition of matrix metalloproteinase activity inhibits smooth muscle cell migration but not neointimal thickening after arterial injury [J].
Bendeck, MP ;
Irvin, C ;
Reidy, MA .
CIRCULATION RESEARCH, 1996, 78 (01) :38-43
[3]   Inhibition of transcription factor NF-κB reduces matrix metalloproteinase-1,-3 and-9 production by vascular smooth muscle cells [J].
Bond, M ;
Chase, AJ ;
Baker, AH ;
Newby, AC .
CARDIOVASCULAR RESEARCH, 2001, 50 (03) :556-565
[4]   Monoclonal antibodies specific for porcine monocytes/macrophages: Macrophage heterogeneity in the pig evidenced by the expression of surface antigens [J].
Bullido, R ;
delMoral, MG ;
Alonso, F ;
Ezquerra, A ;
Zapata, A ;
Sanchez, C ;
Ortino, E ;
Alvarez, B ;
Dominquez, J .
TISSUE ANTIGENS, 1997, 49 (04) :403-413
[5]   Endothelial dysfunction in cardiovascular diseases - The role of oxidant stress [J].
Cai, H ;
Harrison, DG .
CIRCULATION RESEARCH, 2000, 87 (10) :840-844
[6]  
CHAPMAN MJ, 1981, J LIPID RES, V22, P339
[7]   Role of nuclear factor-κB activation in metalloproteinase-1,-3, and-9 secretion by human macrophages in vitro and rabbit foam cells produced in vivo [J].
Chase, AJ ;
Bond, M ;
Crook, MF ;
Newby, AC .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2002, 22 (05) :765-771
[8]  
Collins R, 2002, LANCET, V360, P23, DOI 10.1016/S0140-6736(02)09328-5
[9]  
CONTI M, 1991, CLIN CHEM, V37, P1273
[10]   The atherosclerotic Yucatan animal model to study the arterial response after balloon angioplasty: the natural history of remodeling [J].
de Smet, BJGL ;
van der Zande, J ;
van der Helm, YJM ;
Kuntz, RE ;
Borst, C ;
Post, MJ .
CARDIOVASCULAR RESEARCH, 1998, 39 (01) :224-232