Anti‑inflammatory effect of Chrysanthemum zawadskii, peppermint, Glycyrrhiza glabra herbal mixture in lipopolysaccharide‑stimulated RAW264.7 macrophages

Mol Med Rep. 2021 Jul;24(1):532. doi: 10.3892/mmr.2021.12171. Epub 2021 May 26.

Abstract

The normal inflammatory reaction protects the body from harmful external factors, whereas abnormal chronic inflammation can cause various diseases, including cancer. The purpose of the present study was to investigate the anti‑inflammatory activity of a mixture of Chrysanthemum zawadskii, peppermint and Glycyrrhiza glabra (CPG) by analyzing the expression levels of inflammatory mediators, cytokines and transcription factors in lipopolysaccharide (LPS)‑stimulated Raw264.7 cells. A nitric oxide assay, ELISA, western blotting and immunofluorescence staining were performed to investigate the anti‑inflammatory activity of the CPG mixture. Pretreatment of Raw264.7 cells with CPG inhibited the increase of inflammatory mediators (inducible nitric oxide synthase, cyclooxygenase‑2 and IFN‑β) induced by LPS. Additionally, it inhibited the production of pro‑inflammatory cytokines (TNF‑α, IL‑6 and IL‑1β). CPG suppressed LPS‑induced phosphorylation of STAT1, AKT, Iκb and NF‑κB. Furthermore, CPG inhibited the translocation of NF‑κB into the nucleus. In summary, CPG could inhibit LPS‑induced inflammation, which occurs primarily through the AKT/Iκb/NF‑κB signaling pathway in RAW264.7 cells.

Keywords: Chrysanthemum zawadskii; Glycyrrhiza glabra; NF‑κB; STAT1; anti‑inflammation; herbal mixture; peppermint.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / pharmacology*
  • Cell Survival / drug effects
  • Chrysanthemum / chemistry*
  • Cyclooxygenase 2 / metabolism
  • Cytokines / metabolism
  • Dinoprostone / metabolism
  • Free Radical Scavengers / pharmacology*
  • Glycyrrhiza / chemistry*
  • Heme Oxygenase-1 / metabolism
  • Inflammation / chemically induced
  • Inflammation / metabolism
  • Lipopolysaccharides / toxicity
  • Macrophages / cytology
  • Macrophages / drug effects*
  • Macrophages / metabolism
  • Membrane Proteins / metabolism
  • Mentha piperita / chemistry*
  • Mice
  • NF-kappa B / antagonists & inhibitors
  • NF-kappa B / metabolism
  • Nitric Oxide / metabolism
  • Nitric Oxide Synthase Type II / metabolism
  • Plant Extracts / pharmacology*
  • Proto-Oncogene Proteins c-akt / antagonists & inhibitors
  • Proto-Oncogene Proteins c-akt / metabolism
  • RAW 264.7 Cells
  • STAT1 Transcription Factor / metabolism
  • Signal Transduction / drug effects

Substances

  • Anti-Inflammatory Agents
  • Cytokines
  • Free Radical Scavengers
  • Lipopolysaccharides
  • Membrane Proteins
  • NF-kappa B
  • Plant Extracts
  • STAT1 Transcription Factor
  • Stat1 protein, mouse
  • Nitric Oxide
  • Nitric Oxide Synthase Type II
  • Nos2 protein, mouse
  • Heme Oxygenase-1
  • Hmox1 protein, mouse
  • Cyclooxygenase 2
  • Proto-Oncogene Proteins c-akt
  • Dinoprostone

Grants and funding

The Ministry of Trade, Industry, and Energy (MOTIE), Korea, under the ‘Regional Specialized Industry Development Program (grant no. S2913418)’ supervised by the Korea Institute for Advancement of Technology (KIAT) financially supported this research.