Rosuvastatin Inhibits MMP-2 Expression and Limits the Progression of Atherosclerosis in LDLR-deficient Mice

被引:43
作者
Guo, Hangyuan [1 ,3 ]
Shi, Yafei [3 ]
Liu, Longbin [1 ]
Sun, Aijing [2 ]
Xu, Fukang [1 ]
Chi, Jufang [1 ]
机构
[1] Shaoxing Peoples Hosp, Dept Cardiol, Shaoxing 312000, Zhejiang, Peoples R China
[2] Shaoxing Peoples Hosp, Dept Pathol, Shaoxing 312000, Zhejiang, Peoples R China
[3] Wenzhou Med Coll, Wenzhou City, Zhejiang, Peoples R China
关键词
Rosuvastatin; MMP-2; Atherosclerosis; LDLR-deficient mice; RENIN-ANGIOTENSIN SYSTEM; MATRIX METALLOPROTEINASES; APOLIPOPROTEIN-E; ARTERIAL INJURY; ATHEROGENESIS; OVEREXPRESSION; DYSLIPIDEMIA; ANTIOXIDANT; SIMVASTATIN; MACROPHAGES;
D O I
10.1016/j.arcmed.2009.07.006
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background and Aims. Statins have been shown to reduce morbidity and mortality of coronary heart disease (CHID). Matrix metalloproteinases (MMPs) have been found to be involved in atherosclerotic plaque growth and instability. Rosuvastatin may inhibit the secretion of MMP-2 and MMP-9 from vascular smooth muscle cells and macrophages in vitro. The present study investigated the effects of rosuvastatin on the progression of atherosclerosis and the expression of MMP-2/-9 in LDLR-deficient mice. Methods. LDLR-deficient mice were included in rosuvastatin group and control group on a high-fat and high-cholesterol diet. After 12 weeks, we randomly sacrificed and examined the atherosclerotic lesion area in aortic artery and aortic sinus and levels of plasma lipid, glucose and insulin and expression of MMP-2 and MMP-9 in the atherosclerotic plaques. Results. Atherosclerotic lesion area was significantly decreased in rosuvastatin group vs. control group. Meanwhile, levels of plasma total cholesterol (TC), triglycerides (TG), low-density lipoprotein cholesterol (LDL-C), and oxidized (ox)LDL in the rosuvastatin group were decreased as well as MMP-2 and MMP-9 expression in aortic arch with gelatin zymography and the production of MMP-2 in the aortic sinus through immunohistochemical methods. Levels of plasma high-density lipoprotein cholesterol (HDLC), glucose and insulin were also decreased in rosuvastatin group but failed to achieve statistical significance compared with control group. Interestingly, we found that the value of HDL-C/TC ratio was increased in rosuvastatin group. Conclusions. Rosuvastatin inhibits the expression of MMP-2/-9 and limits the progression of atherosclerosis in LDLR-deficient mice. This may be one of the pathways of rosuvastatin on atherosclerosis through which rosuvastatin induced its benefit to the therapy of coronary heart disease (CHD). (C) 2009 IMSS. Published by Elsevier Inc.
引用
收藏
页码:345 / 351
页数:7
相关论文
共 24 条
[1]   In vitro anti-oxidant and dna protective effects of the novel 3-hydroxy-3-methylglutaryl coenzyme a reductase inhibitor rosuvastatin [J].
Ajith, T. A. ;
Riji, T. ;
Anu, V. .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2008, 35 (5-6) :625-629
[2]   Cross-talk between dyslipidemia and renin-angiotensin system and the role of LOX-1 and MAPK in atherogenesis - Studies with the combined use of rosuvastatin and candesartan [J].
Chen, JW ;
Li, DY ;
Schaefer, R ;
Mehta, JL .
ATHEROSCLEROSIS, 2006, 184 (02) :295-301
[3]   Inhibitory effect of candesartan and rosuvastatin on CD40 and MMPs expression in apo-E knockout mice - Novel insights into the role of RAS and dyslipidemid in atherogenesis [J].
Chen, JW ;
Li, DY ;
Schaefer, RF ;
Mehta, JL .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2004, 44 (04) :446-452
[4]   Green tea catechins inhibit neointimal hyperplasia in a rat carotid arterial injury model by TIMP-2 overexpression [J].
Cheng, XW ;
Kuzuya, M ;
Sasaki, T ;
Kanda, S ;
Tamaya-Mori, N ;
Koike, T ;
Maeda, K ;
Nishitani, E ;
Iguchi, A .
CARDIOVASCULAR RESEARCH, 2004, 62 (03) :594-602
[5]   Effects of simvastatin on plasma lipoproteins and response to arterial injury in wild-type and apolipoprotein-E-deficient mice [J].
Choudhury, RP ;
Carrelli, AL ;
Stern, JD ;
Chereshnev, I ;
Soccio, R ;
Elmalema, VI ;
Fallon, JT ;
Fisher, EA ;
Reisb, ED .
JOURNAL OF VASCULAR RESEARCH, 2004, 41 (01) :75-83
[6]   Differential effects of amlodipine and atorvastatin treatment and their combination on atherosclerosis in ApoE*3-Leiden transgenic mice [J].
Delsing, DJM ;
Jukema, JW ;
van de Wiel, MA ;
Emeis, JJ ;
van der Laarse, A ;
Havekes, LM ;
Princen, HMG .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2003, 42 (01) :63-70
[7]   Matrix metalloproteinases and tissue inhibitors of metalloproteinases in hamster aortic atherosclerosis: correlation with in-situ zymography [J].
Faia, KL ;
Davis, WP ;
Marone, AJ ;
Foxall, TL .
ATHEROSCLEROSIS, 2002, 160 (02) :325-337
[8]   Targeted disruption of the matrix metalloproteinase-9 gene impairs smooth muscle cell migration arterial remodeling and geometrical [J].
Galis, ZS ;
Johnson, C ;
Godin, D ;
Magid, R ;
Shipley, JM ;
Senior, RM ;
Ivan, E .
CIRCULATION RESEARCH, 2002, 91 (09) :852-859
[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]   Matrix metalloproteinases in vascular remodeling and atherogenesis - The good, the bad, and the ugly [J].
Galis, ZS ;
Khatri, JJ .
CIRCULATION RESEARCH, 2002, 90 (03) :251-262