Statins prevent oxidized low-density lipoprotein- and lysophosphatidylcholine-induced proliferation of human endothelial cells

被引:35
作者
Schaefer, CA [1 ]
Kuhlmann, CRW [1 ]
Gast, C [1 ]
Weiterer, S [1 ]
Li, F [1 ]
Most, AK [1 ]
Neumann, T [1 ]
Backenköhler, U [1 ]
Tillmanns, H [1 ]
Waldecker, B [1 ]
Wiecha, J [1 ]
Erdogan, A [1 ]
机构
[1] Univ Giessen, Dept Cardiol & Angiol, D-35392 Giessen, Germany
关键词
statin; proliferation; oxLDL; lysophosphatidylcholine; endothelial cells;
D O I
10.1016/j.vph.2004.05.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The proliferation of endothelial cells is induced by oxidized low-density lipoprotein (oxLDL) and its major component, lysophosphatidylcholine (LPC). The aim of this study was to investigate the effect of statins on the proliferation of endothelial cells derived from human umbilical cord veins (HUVEC). Cerivastatin, simvastatin and fluvastatin caused a dose-dependent inhibition of endothelial cell growth (n = 12; P < .01) when using cell counts and [H-3]-thymidine incorporation, respectively. The strongest inhibition of HUVEC proliferation was achieved at statin concentrations of 0.1 mumol/l (cerivastatin), 2.5 mumol/l (simvastatin) and 1 mumol/l (fluvastatin). Cell counts were significantly reduced from 22937 +/- 280.6 (control) to 7791 +/- 133.6 (cerivastatin), 7292 +/- 146.6 (simvastatin) and 6792 +/- 135.5 (fluvastatin) (n = 12-1 P < .01). Interestingly, cell proliferation induced by oxLDL (10 mug/ml) and LPC (20 mumol/l) could be effectively prevented using statins at concentrations between 0.01 and 0.1 mumol/l (cerivastatin), 1 and 2.5 mumol/l (simvastatin) and 0.25 and 1 mumol/l (fluvastatin). This effect of the statins was abolished by preincubation with mevalonate (500 mumol/1). Our results demonstrate an interesting direct effect of statins on the proliferation of human endothelial cells induced by oxLDL and LPC, which may be beneficial to prevent vascular effects of these atherogenic lipids. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:67 / 73
页数:7
相关论文
共 22 条
[1]   Potential role for ceramide in mitogen-activated protein kinase activation and proliferation of vascular smooth muscle cells induced by oxidized low density lipoprotein [J].
Augé, N ;
Escargueil-Blanc, I ;
Lajoie-Mazenc, I ;
Suc, I ;
Andrieu-Abadie, N ;
Pieraggi, MT ;
Chatelut, M ;
Thiers, JC ;
Jaffrézou, JP ;
Laurent, G ;
Levade, T ;
Nègre-Salvayre, A ;
Salvayre, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (21) :12893-12900
[2]   Effects of cerivastatin on human arterial smooth muscle cell proliferation and migration in transfilter cocultures [J].
Axel, DI ;
Riessen, R ;
Runge, H ;
Viebahn, R ;
Karsch, KR .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2000, 35 (04) :619-629
[3]   Hypertriglyceridemia: A review of clinical relevance and treatment options: Focus on cerivastatin [J].
Breuer, HWM .
CURRENT MEDICAL RESEARCH AND OPINION, 2001, 17 (01) :60-73
[4]   INCREASED ENDOTHELIAL CELL TURNOVER IN AREAS OF IN-VIVO EVANS-BLUE UPTAKE IN PIG AORTA [J].
CAPLAN, BA ;
SCHWARTZ, CJ .
ATHEROSCLEROSIS, 1973, 17 (03) :401-417
[5]   Cell death in human atherosclerotic plaques involves both oncosis and apoptosis [J].
Crisby, M ;
Kallin, B ;
Thyberg, J ;
Zhivotovsky, B ;
Orrenius, S ;
Kostulas, V ;
Nilsson, J .
ATHEROSCLEROSIS, 1997, 130 (1-2) :17-27
[6]  
Dobrucki L W, 2001, Med Sci Monit, V7, P622
[7]   EFFECTS OF NATIVE AND OXIDIZED LOW-DENSITY LIPOPROTEINS ON FORMATION AND INACTIVATION OF ENDOTHELIUM-DERIVED RELAXING FACTOR [J].
GALLE, J ;
MULSCH, A ;
BUSSE, R ;
BASSENGE, E .
ARTERIOSCLEROSIS AND THROMBOSIS, 1991, 11 (01) :198-203
[8]  
Heinloth A, 2000, J AM SOC NEPHROL, V11, P1819, DOI 10.1681/ASN.V11101819
[9]   Nitric oxide inhibits proliferation of human endothelial cells via a mechanism independent of cGMP [J].
Heller, R ;
Polack, T ;
Gräbner, R ;
Till, U .
ATHEROSCLEROSIS, 1999, 144 (01) :49-57
[10]   CULTURE OF HUMAN ENDOTHELIAL CELLS DERIVED FROM UMBILICAL VEINS - IDENTIFICATION BY MORPHOLOGIC AND IMMUNOLOGICAL CRITERIA [J].
JAFFE, EA ;
NACHMAN, RL ;
BECKER, CG ;
MINICK, CR .
JOURNAL OF CLINICAL INVESTIGATION, 1973, 52 (11) :2745-2756