期刊
CELLULAR PHYSIOLOGY AND BIOCHEMISTRY
卷 30, 期 3, 页码 609-617出版社
KARGER
DOI: 10.1159/000341442
关键词
Ketamine; Astrocyte; Inflammation; TLR4; NF-KB kappa; GFAP; Cytokine
资金
- National Natural Science Foundation of China [81171013, 81070889, 81001431, 81171041]
- Key Subject of Colleges and Universities Natural Science Foundation of Jiangsu Province [10KJA320052]
- Natural Science Foundation of Jiangsu Higher Education Institutions of China [11KJB310014]
- Xuzhou Scientific and Technological Project [xzzd1052]
- Priority Academic Program Development of Jiangsu Higher Education Institutions
Background/Aims: Ketamine has been reported to exert anti-inflammatory effects on astrocytes stimulated by lipopolysaccharide (LPS) in vitro and in vivo. However, the mechanism has not been elicited clearly. The aim of this study was to investigate the effects of ketamine on TLR4 expression and NF-kappa B-p65 phosphorylation, as well as the production of proinflammatory cytokines in LPS challenged astrocytes. Methods: Astrocytes were stimulated with LPS (1 mu g/ml) in the absence and presence of various concentrations of ketamine (10, 100, 1000 mu M). The concentrations of IL-1 beta, IL-6 and TNF-alpha were measured by ELISA, the expression of glial fibrillary acidic protein (GFAP) in astrocytes was detected by immunofluorescence staining, the level of phosphorylated NF-kappa B p65 and the expression of TLR4 were detected by western blotting. Results: LPS increased TLR4 expression and the phosphorylation of NF-kappa B p65 subunit as well as GFAP expression and the production of IL-1 beta, IL-6 and TNF-alpha in cultured astrocytes. Ketamine (100 and 1000 mu M) reduced the expression of GFAP and the production of these proinflammatory cytokines, inhibited the expression of TLR4 and attenuated the phosphorylation of NF-kappa B p65 in astrocytes challenged by LPS. Conclusion: The inhibitory effects of ketamine on LPS-induced astrocytes activation and inflammation response may be mediated by suppressing NF-kappa B activation through reducing the expression of TLR4. Copyright (c) 2012 S. Karger AG, Basel
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