Atorvastatin activates PPAR-γ and attenuates the inflammatory response in human monocytes

被引:143
作者
Grip, O [1 ]
Janciauskiene, S [1 ]
Lindgren, S [1 ]
机构
[1] Univ Lund, Univ Hosp MAS, Dept Med, Gastroenterol & Hepatol Div, SE-20502 Malmo, Sweden
关键词
atorvastatin; monocytes; inflammation; PPAR-gamma;
D O I
10.1007/BF02684000
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Objective: To investigate the ability of statins to activate the nuclear receptor peroxisome proliferator-activated receptor gamma (PPAR-gamma) in primary human monocytes in culture. Materials and methods: Human peripheral monocytes were incubated with atorvastatin (0.1-10 mumol/l) for up to 24 hours. PPAR-gamma expression was analysed by electrophoretic mobility shift assay. Pro-inflammatory cytokines were measured by enzyme-linked immunosorbent assays, and oxygen consumption was determined polarographically with a Clark-type oxygen electrode. Results: We found that atorvastatin activates PPAR-gamma and inhibits the production of tumour necrosis factor-alpha up to 38% (p < 0.05), monocyte chemoattractant protein-1 up to 85% (p < 0.05), and gelatinase B up to 73% (p < 0.05), in a concentration-dependent manner. Moreover, atorvastatin shows concentration-dependent inhibition of cellular oxygen consumption up to 41%. Conclusions: These findings contribute to the growing knowledge of the anti-inflammatory effects of statins, and have led us to the suggestion that statins may control inflammatory responses by the regulation of intracellular lipid homeostasis.
引用
收藏
页码:58 / 62
页数:5
相关论文
共 35 条
[31]   Activation of peroxisome proliferator-activated receptor γ does not inhibit IL-6 or TNF-α responses of macrophages to lipopolysaccharide in vitro or in vivo [J].
Thieringer, R ;
Fenyk-Melody, JE ;
Le Grand, CB ;
Shelton, BA ;
Detmers, PA ;
Somers, EP ;
Carbin, L ;
Moller, DE ;
Wright, SD ;
Berger, J .
JOURNAL OF IMMUNOLOGY, 2000, 164 (02) :1046-1054
[32]   PPARγ promotes monocyte/macrophage differentiation and uptake of oxidized LDL [J].
Tontonoz, P ;
Nagy, L ;
Alvarez, JGA ;
Thomazy, VA ;
Evans, RM .
CELL, 1998, 93 (02) :241-252
[33]   HMG-CoA reductase inhibitors decrease CD11b expression and CD11b-dependent adhesion of monocytes to endothelium and reduce increased adhesiveness of monocytes isolated from patients with hypercholesterolemia [J].
Weber, C ;
Erl, W ;
Weber, KSC ;
Weber, PC .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1997, 30 (05) :1212-1217
[34]   Oxidative damage and mutation to mitochondrial DNA and age-dependent decline of mitochondrial respiratory function [J].
Wei, YH ;
Lu, CY ;
Lee, HC ;
Pang, CY ;
Ma, YS .
TOWARDS PROLONGATION OF THE HEALTHY LIFE SPAN: PRACTICAL APPROACHES TO INTERVENTION, 1998, 854 :155-170
[35]   NEUTRAL METALLOPROTEINASES PRODUCED BY HUMAN MONONUCLEAR PHAGOCYTES - ENZYME PROFILE, REGULATION, AND EXPRESSION DURING CELLULAR-DEVELOPMENT [J].
WELGUS, HG ;
CAMPBELL, EJ ;
CURY, JD ;
EISEN, AZ ;
SENIOR, RM ;
WILHELM, SM ;
GOLDBERG, GI .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (05) :1496-1502