Fluvastatin inhibits matrix metalloproteinase-1 expression in human vascular endothelial cells

被引:104
作者
Ikeda, U [1 ]
Shimpo, M [1 ]
Ohki, R [1 ]
Inaba, H [1 ]
Takahashi, M [1 ]
Yamamoto, K [1 ]
Shimada, K [1 ]
机构
[1] Jichi Med Sch, Dept Cardiol, Minamimaki, Tochigi 3290498, Japan
关键词
atherosclerosis; nitric oxide; extracellular matrix; collagen;
D O I
10.1161/01.HYP.36.3.325
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Matrix metalloproteinase-1 (MMP-1), also called interstitial collagenase, may play an important role in the pathogenesis of atherosclerosis and atherosclerotic plaque rupture. We investigated the effects of fluvastatin on MMP-1 expression in human vascular endothelial cells (ECs). The addition of fluvastatin decreased the basal MMP-1 levels in the culture media of ECs in a time-dependent (0 to 48 hours) and dose-dependent (10(-8) to 10(-5) mol/L) manner. On the other hand, fluvastatin did not affect tissue inhibitor of metalloproteinase-1 levels. Collagenolytic activity in conditioned media of ECs was also dose-dependently reduced by fluvastatin. The effect of fluvastatin on MMP-1 expression was completely reversed in the presence of mevalonate or geranylgeranyl-pyrophosphate, but not in the presence of squalene. Inhibition of Rho by C3 exoenzyme also significantly decreased MMP-1 expression in ECs. Our findings revealed that fluvastatin decreases MMP-1 expression in human vascular ECs through inhibition of Rho.
引用
收藏
页码:325 / 329
页数:5
相关论文
共 27 条
[1]   Inhibitory effect of fluvastatin at doses insufficient to lower serum lipids on the catheter-induced thickening of intima in rabbit femoral artery [J].
Bandoh, T ;
Mitani, H ;
Niihashi, M ;
Kusumi, Y ;
Ishikawa, J ;
Kimura, M ;
Totsuka, T ;
Sakurai, I ;
Hayashi, S .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1996, 315 (01) :37-42
[2]   HMG-CoA reductase inhibitors reduce MMP-9 secretion by macrophages [J].
Bellosta, S ;
Via, D ;
Canavesi, M ;
Pfister, P ;
Fumagalli, R ;
Paoletti, R ;
Bernini, F .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1998, 18 (11) :1671-1678
[3]   REQUIREMENT FOR MEVALONATE IN ACETYLATED LDL INDUCTION OF CHOLESTEROL ESTERIFICATION IN MACROPHAGES [J].
BERNINI, F ;
DIDONI, G ;
BONFADINI, G ;
BELLOSTA, S ;
FUMAGALLI, R .
ATHEROSCLEROSIS, 1993, 104 (1-2) :19-26
[4]   RELATIONSHIP BETWEEN MEVALONATE PATHWAY AND ARTERIAL MYOCYTE PROLIFERATION - IN-VITRO STUDIES WITH INHIBITORS OF HMG-COA REDUCTASE [J].
CORSINI, A ;
MAZZOTTI, M ;
RAITERI, M ;
SOMA, MR ;
GABBIANI, G ;
FUMAGALLI, R ;
PAOLETTI, R .
ATHEROSCLEROSIS, 1993, 101 (01) :117-125
[5]  
CORSINI A, 1995, AM J CARDIOL, V76, P21
[6]   MATRIX METALLOPROTEINASES AND CARDIOVASCULAR-DISEASE [J].
DOLLERY, CM ;
MCEWAN, JR ;
HENNEY, AM .
CIRCULATION RESEARCH, 1995, 77 (05) :863-868
[7]   Effects of amlodipine on gene expression and extracellular matrix formation in human vascular smooth muscle cells and fibroblasts: implications for vascular protection [J].
Eickelberg, O ;
Roth, ML ;
Block, LH .
INTERNATIONAL JOURNAL OF CARDIOLOGY, 1997, 62 :S31-S37
[8]  
GALIS ZS, 1995, ANN NY ACAD SCI, V748, P501
[9]   INCREASED EXPRESSION OF MATRIX METALLOPROTEINASES AND MATRIX-DEGRADING ACTIVITY IN VULNERABLE REGIONS OF HUMAN ATHEROSCLEROTIC PLAQUES [J].
GALIS, ZS ;
SUKHOVA, GK ;
LARK, MW ;
LIBBY, P .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (06) :2493-2503
[10]   Matrilysin is expressed by lipid-laden macrophages at sites of potential rupture in atherosclerotic lesions and localizes to areas of versican deposition, a proteoglycan substrate for the enzyme [J].
Halpert, I ;
Sires, UI ;
Roby, JD ;
PotterPerigo, S ;
Wight, TN ;
Shapiro, SD ;
Welgus, HG ;
Wickline, SA ;
Parks, WC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (18) :9748-9753