Suppressive effects of alloxanthin and diatoxanthin from Halocynthia roretzi on LPS-induced expression of pro-inflammatory genes in RAW264.7 cells

J Oleo Sci. 2008;57(3):181-9. doi: 10.5650/jos.57.181.

Abstract

To investigate anti-inflammatory effects of carotenoids from Halocynthia roretzi, gene expression levels were measured for pro-inflammatory cytokines and enzymes in the murine macrophage-like cell line, RAW264.7, stimulated with lipopolysaccharide (LPS). All-trans alloxanthin, all-trans diatoxanthin, and their 9-cis isomers isolated from H. roretzi significantly suppressed expression of IL-1beta and IL-6 mRNA in cells induced by LPS without cytotoxicity. The expression level of IL-1beta mRNA in cells treated with 25 microM all-trans alloxanthin for 24 h, followed by stimulation with 0.1 microg/mL LPS for 24 h in the presence of carotenoid decreased to 33.7+/-3.0% from that of control cells stimulated with LPS alone. All-trans diatoxanthin, 9-cis alloxanthin and 9-cis diatoxanthin also decreased expression of IL-1beta mRNA to 25.1+/-2.1, 28.2+/-0.9 and 32.9+/-3.3%, respectively, from that of control cells stimulated with LPS. IL-1beta production in culture medium was also suppressed by all-trans alloxanthin and all-trans diatoxanthin. Furthermore, all-trans alloxanthin, all-trans diatoxanthin and their 9-cis isomers suppressed the over-expression of cyclooxygenase-2 and nitric oxide synthase mRNA in RAW264.7 cells induced by LPS. The suppressive effects of these carotenoids were remarkable compared to those of beta-carotene and zeaxanthin.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carotenoids / isolation & purification
  • Carotenoids / pharmacology
  • Cell Line
  • Cell Survival / drug effects
  • Cell Survival / genetics
  • Gene Expression Regulation / drug effects*
  • Gene Expression Regulation / physiology
  • Inflammation Mediators / antagonists & inhibitors*
  • Inflammation Mediators / metabolism*
  • Lipopolysaccharides / toxicity*
  • Mice
  • Urochordata*
  • Xanthophylls / isolation & purification
  • Xanthophylls / pharmacology*
  • Xanthophylls / therapeutic use

Substances

  • Inflammation Mediators
  • Lipopolysaccharides
  • Xanthophylls
  • Carotenoids
  • diatoxanthin
  • alloxanthin