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

作者信息

Grip O, Janciauskiene S, Lindgren S

机构信息

Department of Medicine, Lund University, University Hospital MAS, Malmö, Sweden.

出版信息

Inflamm Res. 2002 Feb;51(2):58-62. doi: 10.1007/BF02684000.

DOI:10.1007/BF02684000
PMID:11926313
Abstract

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 micromol/1) 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.

摘要

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A PPAR gamma-LXR-ABCA1 pathway in macrophages is involved in cholesterol efflux and atherogenesis.巨噬细胞中的过氧化物酶体增殖物激活受体γ-肝X受体-ATP结合盒转运蛋白A1途径参与胆固醇外流和动脉粥样硬化的发生。
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