Pro-inflammatory cytokine gene expression and nitric oxide regulation of aqueous extracted Astragali radix in RAW 264.7 macrophage cells

Lee, Y, Han, O, Park, C, Yang, C, Jeon, T, Yoo, W, Kim, S and Kim, H 2005, 'Pro-inflammatory cytokine gene expression and nitric oxide regulation of aqueous extracted Astragali radix in RAW 264.7 macrophage cells', Journal of Ethnopharmacology, vol. 100, pp. 289-294.


Document type: Journal Article
Collection: Journal Articles

Title Pro-inflammatory cytokine gene expression and nitric oxide regulation of aqueous extracted Astragali radix in RAW 264.7 macrophage cells
Author(s) Lee, Y
Han, O
Park, C
Yang, C
Jeon, T
Yoo, W
Kim, S
Kim, H
Year 2005
Journal name Journal of Ethnopharmacology
Volume number 100
Start page 289
End page 294
Total pages 6
Publisher Elsevier
Abstract Astragali radix, which has tonifying and circulatory effect as well as immune response, is one of the oldest and most frequently used crude drug for oriental medicine in many Asian countries. The present study was conducted to evaluate the effect of aqueous extract of Astragali radix (ARE) on the functions of murine macrophage cell line, RAW 264.7 macrophage cells. In the cell proliferation assay, methotrexate (MTX), an agent of immune suppression, decreased the cell proliferation of RAW 264.7 macrophage cells (IC50: 100 mu g/ml), but the suppression of cell proliferation was significantly protected by ARE treatment in RAW 264.7 macrophage cells. The expressions of cytokine gene by ARE were investigated using reverse transcription polymerase chain reaction (RT-PCR). In RT-PCR, IL-1 alpha, IL-1 beta and IL-6 mRNA expressions was induced in ARE-treated RAW 264.7 macrophage cells. We also investigated the effect of the nitric oxide (NO) synthesis and inducible nitric oxide synthase (iNOS) mRNA expression by ARE. ARE alone had no effect on NO synthesis and iNOS mRNA expression in RAW 264.7 cells. In the case of lipopolysaccharide (LPS) stimulation, NO production and iNOS mRNA expression were detected in RAW 264.7 cells. However, NO production and iNOS mRNA expression which is induced by LPS decreased after treatment of ARE. These data demonstrate that ARE can reduce the suppression of macrophage cell proliferation induced by MTX, and induce IL-1 alpha, IL-1 beta and IL-6 mRNA expressions in RAW 264.7 macrophage cells. Also, ARE inhibit NO production in LPS-stimulated RAW 264.7 macrophage cells, and the inhibition of NO production may be associated with the inhibition of iNOS mRNA expression.
Subject Traditional Chinese Medicine and Treatments
Keyword(s) Astragali radix
Cytokine
NO
RAW 264.7 macrophage cells
DOI - identifier 10.1016/j.jep.2005.03.009
Copyright notice Copyright © 2005 Elsevier Ireland Ltd All rights reserved.
ISSN 0378-8741
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