Planta Med 2018; 84(08): 527-535
DOI: 10.1055/s-0043-123349
Biological and Pharmacological Activity
Original Papers
Georg Thieme Verlag KG Stuttgart · New York

Anti-inflammatory Effects of Canthin-6-one Alkaloids from Ailanthus altissima

Authors

  • Seung-Kye Cho

    1   Department of Life and Nanopharmaceutical Sciences, Kyung Hee University, Seoul, Korea
  • Miran Jeong

    1   Department of Life and Nanopharmaceutical Sciences, Kyung Hee University, Seoul, Korea
  • Dae Sik Jang

    1   Department of Life and Nanopharmaceutical Sciences, Kyung Hee University, Seoul, Korea
    2   Department of Pharmaceutical Science, College of Pharmacy, Kyung Hee University, Seoul, Korea
  • Jung-Hye Choi

    1   Department of Life and Nanopharmaceutical Sciences, Kyung Hee University, Seoul, Korea
    3   Department of Oriental Pharmaceutical Science, College of Pharmacy, Kyung Hee University, Seoul, Korea
Further Information

Publication History

received 02 September 2017
revised 07 November 2017

accepted 15 November 2017

Publication Date:
27 November 2017 (online)

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.

Supporting Information