期刊
JOURNAL OF MEDICINAL FOOD
卷 16, 期 11, 页码 997-1003出版社
MARY ANN LIEBERT, INC
DOI: 10.1089/jmf.2012.2473
关键词
[Ca2+]i; COX-2; iNOS; NF-B; NO; PGE(2); salidroside
资金
- National Nature Science Foundation of China [30972212]
The aim of this study was to evaluate the effect of salidroside on lipopolysaccharide (LPS)-induced nitric oxide (NO) and prostaglandin E-2 (PGE(2)) production in RAW 264.7 macrophages and related anti-inflammatory mechanism. PGE(2) production was measured by enzyme-linked immunosorbent assay (ELISA); NO production was tested by Griess reagent. Inducible nitric oxidesynthase (iNOS) and COX-2 were determined by RT-PCR and Western blot analysis; IB and P-IB protein express were detected by Western blot analysis; cytosolic free Ca2+ ([Ca2+]i)was measured by a fluorescent microscope. The data showed salidroside inhibited LPS-induced NO and PGE(2) production and reduced iNOS and COX-2 protein expression in RAW 264.7 macrophages. Consistent with these observations, salidroside inhibited LPS-induced cytosolic free Ca2+ concentration ([Ca2+]i) elevation. In addition, we further investigated signal transduction mechanisms and found that the activation of NF-B was suppressed by salidroside in a dose-dependent manner. These results suggest that salidroside suppresses NO and PGE(2) production by inhibiting iNOS and COX-2 protein expression, level of [Ca2+]i, and activation of NF-B signal transduction pathway.
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