Abstract
Canthin-6-one (CO) alkaloids possess various biological activities, including antibacterial,
antitumor, antifungal, and antiviral activities. However, their anti-inflammatory
effects and underlying molecular mechanisms are poorly characterized. This study aimed
to investigate the anti-inflammatory effects of CO and its derivative 5-(1-hydroxyethyl)-canthin-6-one
(5-HCO), isolated from the stem barks of Ailanthus altissima in lipopolysaccharide (LPS)-stimulated macrophages. CO (1 and 5 µM) and 5-HCO (7.5
and 15 µM) significantly inhibited the LPS-induced expression of inducible nitric
oxide synthase. In addition, CO (1 and 5 µM) and 5-HCO (15 µM) markedly suppressed
the production of prostaglandin E2 (PGE2) and expression of cyclooxygenase-2, a key enzyme in PGE2 synthesis, in LPS-stimulated macrophages. Moreover, CO treatment significantly reduced
monocyte chemotactic protein-1 (MCP-1) and tumor necrosis factor-α (TNF-α) expression, whereas 5-HCO inhibited MCP-1, but not TNF-α expression. Both CO and 5-HCO inhibited the phosphorylation of inhibitor kappa B
and transcriptional activation of nuclear factor kappa B (NF-κB) in LPS-stimulated macrophages. In addition, CO, but not 5-HCO, markedly reduced
Akt phosphorylation. Taken together, these data suggest that CO, but not 5-HCO with
a hydroxyethyl moiety on the D ring, has potent anti-inflammatory activity in LPS-stimulated
macrophages through the downregulation of both the NF-κB and the Akt pathway.
Key words
Ailanthus altissima
- Simaroubaceae - alkaloids - canthin-6-one - 5-(1-hydroxyethyl)-canthin-6-one - inflammation
- NF-
κB