Anti-Inflammatory Activity of the Combination of Nobiletin and Docosahexaenoic Acid in Lipopolysaccharide-Stimulated RAW 264.7 Cells: A Potential Synergistic Anti-Inflammatory Effect

Nutrients. 2024 Jun 29;16(13):2080. doi: 10.3390/nu16132080.

Abstract

This study aimed to investigate a synergistic anti-inflammatory effect of a citrus flavonoid nobiletin and docosahexaenoic acid (DHA), one of n-3 long-chain polyunsaturated fatty acids, in combination. Simultaneous treatment with nobiletin and DHA synergistically inhibited nitric oxide production (combination index < 0.9) by mouse macrophage-like RAW 264.7 cells stimulated with lipopolysaccharide (LPS) without cytotoxicity. On the other hand, the inhibitory effect of nobiletin and DHA in combination on proinflammatory cytokine production was not synergistic. Neither nobiletin nor DHA affected the phagocytotic activity of RAW 264.7 cells stimulated with LPS. Immunoblot analysis revealed that the inhibition potency of DHA on the phosphorylation of ERK and p38 and nuclear translocation of NF-κB is markedly enhanced by simultaneously treating with nobiletin, which may lead to the synergistic anti-inflammatory effect. Overall, our findings show the potential of the synergistic anti-inflammatory effect of nobiletin and DHA in combination.

Keywords: RAW 264.7 cells; docosahexaenoic acid; inflammation; lipopolysaccharide; nobiletin; synergism.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents* / pharmacology
  • Cytokines / metabolism
  • Docosahexaenoic Acids* / pharmacology
  • Drug Synergism*
  • Flavones* / pharmacology
  • Lipopolysaccharides* / pharmacology
  • Macrophages* / drug effects
  • Macrophages* / metabolism
  • Mice
  • NF-kappa B / metabolism
  • Nitric Oxide* / metabolism
  • Phagocytosis / drug effects
  • Phosphorylation / drug effects
  • RAW 264.7 Cells
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • nobiletin
  • Flavones
  • Lipopolysaccharides
  • Anti-Inflammatory Agents
  • Docosahexaenoic Acids
  • Nitric Oxide
  • NF-kappa B
  • Cytokines
  • p38 Mitogen-Activated Protein Kinases

Grants and funding

This research received no external funding.