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Int J Clin Pharmacol Ther ; 45(6): 319-27, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17595889

ABSTRACT

OBJECTIVE: It has been speculated that the reduction in vascular events by statins may not only be due to lowering of cholesterol, but also to the decrease in plasma C-reactive protein (CRP). In the present study we investigated the possibility that rosuvastatin directly affected CRP expression in stimulated human hepatocytes. METHODS: Interleukin 6 (IL-6) stimulated human hepatoma cells (Hep3B) and primary human hepatocytes (PHH) were incubated with various concentrations of rosuvastatin (0.3 - 1 microM) for 24 hours. CRP expression was determined using ELISA and quantitative real-time RT-PCR. The activation of STAT3 and C/EBP was investigated utilizing transcription factor assays (TransAM). RESULTS: IL-6 increased CRP secretion by up to 5-fold in Hep3B and 6.6-fold in PHH. Rosuvastatin reduced CRP expression by 32% and 46% in Hep3B and PHH, respectively. IL-6 increased CRP mRNA up to 32-fold. At 1 microM, rosuvastatin reduced CRP mRNA by 73% compared to IL-6-stimulated cells. IL-6 activated the transcription factors STAT3 and C/EBP up to 2.6-fold and 2.2-fold, respectively. Rosuvastatin (1 microM) attenuated the activation of STAT3 and C/EBP by 48% and 54%, respectively. CONCLUSIONS: Our results show a direct inhibitory effect of rosuvastatin on IL-6-induced expression of CRP in liver cells. Statins may lower CRP by inhibiting its production in the liver rather than by exerting systemic anti-inflammatory effects. The effects of rosuvastatin in reducing the levels of CRP in plasma may have clinical utility in addition to its effects on atherogenic lipoproteins.


Subject(s)
C-Reactive Protein/biosynthesis , CCAAT-Enhancer-Binding Proteins/physiology , Fluorobenzenes/pharmacology , Hepatocytes/metabolism , Hydroxymethylglutaryl-CoA Reductase Inhibitors/pharmacology , Interleukin-6/antagonists & inhibitors , Interleukin-6/pharmacology , Pyrimidines/pharmacology , STAT3 Transcription Factor/physiology , Sulfonamides/pharmacology , Atorvastatin , Cells, Cultured , Hepatocytes/drug effects , Heptanoic Acids/pharmacology , Humans , Immunoassay , Mevalonic Acid/pharmacology , Pyrroles/pharmacology , RNA, Messenger/biosynthesis , RNA, Messenger/genetics , Rosuvastatin Calcium , Transcription Factors
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