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The Anti-inflammatory Effect of Gnaphalium affine Through Inhibition of NF-κB and MAPK in Lipopolysaccharide-Stimulated RAW264.7 Cells and Analysis of Its Phytochemical Components
Ist Teil von
Cell biochemistry and biophysics, 2016-09, Vol.74 (3), p.407-417
Ort / Verlag
New York: Springer US
Erscheinungsjahr
2016
Quelle
MEDLINE
Beschreibungen/Notizen
Gnaphalium affine
is an annual herbaceous plant that is used as a traditional medicine in some Latin American and Asian countries. However, systematic studies on its anti-inflammatory activity and signaling pathways have not yet been reported. In this study, we investigated the anti-inflammatory effect of
G. affine
methanol extract in lipopolysaccharide (LPS)-stimulated RAW 264.7 murine macrophage cells and fractioned the methanol extract into hexane, chloroform, ethyl acetate (EtOAc), butyl alcohol (BuOH), and distilled water (DW) by measuring the generation of nitric oxide (NO).
G. affine
inhibited the generation of NO and prostaglandin E
2
. The chloroform-soluble fraction most effectively inhibited LPS-stimulated NO production. We also examined the cytotoxicity of
G. affine
in three normal cell lines: RAW264.7, HEK293, and HaCaT. Cell viability assays showed that the methanol extract and chloroform-soluble fraction of
G. affine
had no cytotoxic effect on normal cell lines. The expression of pro-inflammatory mediators was also investigated. Western blotting and immunofluorescence showed that
G. affine
reduces the expression of iNOS, COX-2, and MAPKs, as well as activation of NF-κB in LPS-stimulated RAW264.7 cells. RT-PCR showed that
G. affine
also negatively regulates inflammatory cytokines at the gene expression level. Taken together,
G. affine
exerts its anti-inflammatory activity through inhibition of NO generation as a result of inhibiting NF-κB and MAPKs-related inflammatory signaling pathways. In addition, the result of GC–MS analysis revealed the presence of nineteen different types of constituents including guaiacol in the chloroform-soluble fraction of
G. affine
.