Effects of Simvastatin on Proinflammatory Cytokines and Matrix Metalloproteinases in Hypercholesterolemic Individuals

被引:11
|
作者
Nilsson, Lennart [1 ]
Eriksson, Per [2 ]
Cherfan, Pierre [3 ]
Jonasson, Lena [1 ]
机构
[1] Linkoping Univ, Div Cardiovasc Med, Dept Med & Hlth Sci, S-58185 Linkoping, Sweden
[2] Karolinska Univ Hosp, Karolinska Inst, Dept Med, Atherosclerosis Res Unit,Ctr Mol Med, Stockholm, Sweden
[3] Hogland Hosp, Dept Med, Eksjo, Sweden
关键词
statin; hypercholesterolemia; pleiotropic effects; cytokine; matrix metalloproteinase; C-REACTIVE PROTEIN; HUMAN ATHEROSCLEROTIC PLAQUES; PLASMA-CONCENTRATION; REDUCTASE INHIBITOR; TISSUE INHIBITOR; COLLAGEN CONTENT; STATINS; INFLAMMATION; MATRIX-METALLOPROTEINASE-9; EXPRESSION;
D O I
10.1007/s10753-010-9227-y
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Statins are potent lipid-lowering drugs but anti-inflammatory effects have also been suggested. Our aim was to investigate the effects of simvastatin on proinflammatory cytokines and matrix metalloproteinases (MMPs). Eighty hypercholesterolemic men were randomized to simvastatin 40 mg or placebo for 6 weeks. Simvastatin treatment significantly reduced C-reactive protein (CRP) levels while interleukin (IL)-6 levels remained unchanged. The ex vivo release of IL-1 beta and IL-6 was not altered by simvastatin, whereas the release of TNF-alpha and IL-8 increased after 6 weeks of simvastatin treatment. Similarly, the circulating levels of MMP-3 and TIMP-1 remained unaffected by simvastatin while MMP-9 increased. However, none of the effects except for the CRP reduction within the simvastatin group reached statistical significance when compared to the placebo group. Our findings are in contrast to previous in vitro and animal data and question the in vivo relevance of some of the pleiotropic effects of simvastatin.
引用
收藏
页码:225 / 230
页数:6
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