Journal
INFLAMMATION
Volume 40, Issue 4, Pages 1204-1213Publisher
SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s10753-017-0563-z
Keywords
2 alpha-Hydroxyl-3 beta-angeloylcinnamolide; Toll-like receptor 4; Mitogen-activated protein kinases; Acute lung injury; Anti-inflammation
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Funding
- National Natural Science Foundation [8157355, 30700060]
- National New Drug Innovation Major Project of China [2011ZX09307-002-02]
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The herbs of Polygonum jucundum Lindex. (Polygonaceae) is a traditional Chinese medicine for inflammatory diseases. 2 alpha-Hydroxyl-3 beta-angeloylcinnamolide (HAC), a drimane-type sesquiterpenoid, was the major active compound of the ethanol extract of P. jucundum which inhibited the production of inflammatory mediators. However, the biological mechanism of HAC for anti-inflammatory activity has not been reported. In the current study, we investigated whether HAC could suppress the production of inflammatory mediators in lipopolysaccharide (LPS)-induced acute lung injury in mice (ALI) through downregulation of Toll-like receptor 4 (TLR4) and activations of mitogen-activated protein kinases (MAPKs) and inducible protein nitric oxide synthase (iNOS). Moreover, our data indicated that HAC inhibits the overexpression of iNOS and TLR4 in LPS-treated RAW264.7, and also inhibits MAPK signal. These findings suggest that HAC shows anti-inflammatory effects in ALI mice through suppressing TLR4-mediated MAPK pathway in activated macrophages. In addition, six derivatives of HAC obtained by structure modification were investigated for their inhibitory effects on the production of nitric oxide (NO) and tumor necrosis factor-alpha (TNF-alpha), suggesting that the acetylation could increase the inhibition of HAC on TNF-alpha release in LPS-treated RAW264.7 cells. In summary, all these results showed that HAC may be a potential anti-inflammatory lead compound for the treatment of acute lung injury.
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