Extract of Boehmeria nivea Suppresses Mast Cell-Mediated Allergic Inflammation by Inhibiting Mitogen-Activated Protein Kinase and Nuclear Factor-κB

Molecules. 2020 Sep 12;25(18):4178. doi: 10.3390/molecules25184178.

Abstract

Mast cells are effector cells that initiate allergic inflammatory immune responses by inducing inflammatory mediators. Boehmeria nivea (Linn.) Gaudich is a natural herb in the nettle family Urticaceae that possesses numerous pharmacological properties. Despite the various pharmacological benefits of Boehmeria nivea, its effects on allergic inflammation have not yet been determined. Here, we investigated the effect of the ethanol extract of Boehmeria nivea (BNE) on degranulation rat basophilic leukemia (RBL)-2H3 mast cells stimulated with anti-dinitrophenyl (anti-DNP) and bovine serum albumin (BSA) during immunoglobulin E (IgE)-mediated allergic immune response. The results showed inhibition of the release of β-hexosaminidase and histamine from the cells. BNE suppressed pro-inflammatory cytokines (Tumor necrosis factor (TNF)-α, Interleukin (IL)-1β, and IL-6) and reduced T helper (Th)2 cytokine IL-4 expression and/or secretion correlated with the downregulation of p38, extracellular signal-regulated kinases (ERK) mitogen-activated protein kinase (MAPK), and nuclear factor-κB (NF-κB) signaling pathways in treated RBL-2H3 mast cells. In passive cutaneous anaphylaxis, treatment with BNE during IgE-mediated local allergic reaction triggered a reduction in mouse ear pigmentation and thickness. Taken together, these results indicated that BNE suppressed mast cell-mediated inflammation, suggesting that BNE might be a candidate for the treatment of various allergic disorders.

Keywords: Boehmeria nivea; allergic inflammation; cytokines; immunoglobulin E; mast cells.

MeSH terms

  • Anaphylaxis / metabolism
  • Animals
  • Anti-Allergic Agents / pharmacology
  • Boehmeria / chemistry*
  • Cell Line, Tumor
  • Cytokines / metabolism
  • Histamine / chemistry
  • Histamine Release / drug effects
  • Hypersensitivity / drug therapy*
  • Immunoglobulin E / chemistry
  • Inflammation / drug therapy*
  • Inflammation Mediators / metabolism
  • MAP Kinase Signaling System / drug effects*
  • Male
  • Mast Cells / drug effects*
  • Mice
  • Mice, Inbred BALB C
  • NF-kappa B / drug effects*
  • Passive Cutaneous Anaphylaxis / drug effects
  • Pigmentation
  • Plant Extracts / pharmacology*
  • Plant Leaves / chemistry
  • Rats
  • Serum Albumin, Bovine / chemistry
  • beta-N-Acetylhexosaminidases / chemistry

Substances

  • Anti-Allergic Agents
  • Cytokines
  • Inflammation Mediators
  • NF-kappa B
  • Plant Extracts
  • Serum Albumin, Bovine
  • Immunoglobulin E
  • Histamine
  • beta-N-Acetylhexosaminidases