Nepetin, a natural compound from Inulae flos, suppresses degranulation and eicosanoid generation through PLCγ1 and Akt signaling pathways in mast cells

Arch Pharm Res. 2020 Feb;43(2):224-232. doi: 10.1007/s12272-020-01212-7. Epub 2020 Feb 3.

Abstract

Nepetin derived from the flowers of Inula japonica, Inulae flos, has been reported to exert several biological activities, including anti-inflammatory responses. In this study, we evaluated the anti-allergic property of nepetin with its molecular mechanisms in bone marrow-derived mast cells (BMMC) and mice. In this in vitro study, we investigated the inhibitory effects of nepetin on degranulation and generation of leukotriene C4 (LTC4) and prostaglandin D2 (PGD2) in IgE/antigen (Ag)-stimulated BMMC. The effect of nepetin on passive cutaneous anaphylaxis (PCA) reaction was also studied in mice. Nepetin reduced degranulation and LTC4 generation in BMMC. The IgE/Ag-mediated signaling pathway demonstrated that nepetin suppressed intracellular Ca2+ level and activation of PLCγ1 and cPLA2. However, MAPKs were not affected by nepetin in BMMC. In addition, nepetin treatment reduced PGD2 production and suppressed cyclooxygenase-2 protein expression via the inhibition of the Akt and nuclear factor-κB signaling pathways. With respect to the local allergic response in vivo, oral administration of nepetin suppressed mast cell-dependent PCA reaction in a dose-dependent manner. The results of this study suggest that nepetin might have an anti-allergic potential related to mast cell-mediated inflammatory diseases.

Keywords: Anti-inflammatory; BMMC; Nepetin; Passive cutaneous anaphylaxis (PCA).

MeSH terms

  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / chemistry
  • Anti-Inflammatory Agents, Non-Steroidal / isolation & purification
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology*
  • Biological Products / chemistry
  • Biological Products / isolation & purification
  • Biological Products / pharmacology*
  • Cell Survival / drug effects
  • Dose-Response Relationship, Drug
  • Flavones / chemistry
  • Flavones / isolation & purification
  • Flavones / pharmacology*
  • Inula / chemistry*
  • Leukotriene C4 / antagonists & inhibitors*
  • Leukotriene C4 / metabolism
  • Male
  • Mast Cells / drug effects
  • Mast Cells / metabolism
  • Mice
  • Mice, Inbred BALB C
  • Molecular Structure
  • Phospholipase C gamma / antagonists & inhibitors
  • Phospholipase C gamma / metabolism
  • Prostaglandin D2 / antagonists & inhibitors*
  • Prostaglandin D2 / metabolism
  • Proto-Oncogene Proteins c-akt / antagonists & inhibitors
  • Proto-Oncogene Proteins c-akt / metabolism
  • Signal Transduction / drug effects
  • Structure-Activity Relationship

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Biological Products
  • Flavones
  • Leukotriene C4
  • Proto-Oncogene Proteins c-akt
  • Phospholipase C gamma
  • eupafolin
  • Prostaglandin D2