Anti-allergic effects of Lycopus lucidus on mast cell-mediated allergy model

Toxicol Appl Pharmacol. 2005 Dec 15;209(3):255-62. doi: 10.1016/j.taap.2005.04.011. Epub 2005 Jun 2.

Abstract

The current study characterizes the mechanism by which the aqueous extract of Lycopus lucidus Turcz. (Labiatae) (LAE) decreases mast cell-mediated immediate-type allergic reaction. The immediate-type allergic reaction is involved in many allergic diseases such as asthma and allergic rhinitis. LAE has been used as a traditional medicine in Korea and is known to have an anti-inflammatory effect. However, its specific mechanism of action is still unknown. LAE was anally administered to mice for high and fast absorption. LAE inhibited compound 48/80-induced systemic reactions in mice. LAE decreased the local allergic reaction, passive cutaneous anaphylaxis, activated by anti-dinitrophenyl (DNP) IgE antibody. LAE dose-dependently reduced histamine release from rat peritoneal mast cells activated by compound 48/80 or anti-DNP IgE. Furthermore, LAE decreased the secretion of TNF-alpha and IL-6 in phorbol 12-myristate 13-acetate (PMA) plus calcium ionophore A23187-stimulated human mast cells. The inhibitory effect of LAE on the pro-inflammatory cytokine was p38 mitogen-activated protein kinase (MAPK) and nuclear factor-kappaB (NF-kappaB) dependent. LAE attenuated PMA plus A23187-induced degradation of IkappaBalpha and nuclear translocation of NF-kappaB, and specifically blocked activation of p38 MAPK, but not that of c-jun N-terminal kinase and extracellular signal-regulated kinase. Our findings provide evidence that LAE inhibits mast cell-derived immediate-type allergic reactions and involvement of pro-inflammatory cytokines, p38 MAPK, and NF-kappaB in these effects.

Publication types

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

MeSH terms

  • Administration, Rectal
  • Animals
  • Anti-Allergic Agents / administration & dosage
  • Anti-Allergic Agents / pharmacology*
  • Anti-Allergic Agents / therapeutic use
  • Calcimycin / pharmacology
  • Calcium / metabolism
  • Cell Line
  • Dinitrophenols / administration & dosage
  • Dinitrophenols / toxicity
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Drug Eruptions / etiology
  • Drug Eruptions / metabolism
  • Drug Eruptions / prevention & control
  • Drug Hypersensitivity / drug therapy
  • Drug Hypersensitivity / etiology
  • Drug Hypersensitivity / metabolism
  • Drugs, Chinese Herbal / administration & dosage
  • Drugs, Chinese Herbal / pharmacology
  • Drugs, Chinese Herbal / therapeutic use
  • Histamine Release / drug effects
  • Humans
  • I-kappa B Proteins / metabolism
  • Injections, Intraperitoneal
  • Interleukin-6 / metabolism
  • Lycopus / chemistry*
  • Male
  • Mast Cells / drug effects*
  • Mast Cells / immunology
  • Mice
  • Mice, Inbred ICR
  • NF-KappaB Inhibitor alpha
  • NF-kappa B / metabolism
  • Phytotherapy
  • Rats
  • Rats, Sprague-Dawley
  • Tetradecanoylphorbol Acetate / analogs & derivatives
  • Tetradecanoylphorbol Acetate / pharmacology
  • Tumor Necrosis Factor-alpha / metabolism
  • p-Methoxy-N-methylphenethylamine / administration & dosage
  • p-Methoxy-N-methylphenethylamine / toxicity
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Anti-Allergic Agents
  • Dinitrophenols
  • Drugs, Chinese Herbal
  • I-kappa B Proteins
  • Interleukin-6
  • NF-kappa B
  • NFKBIA protein, human
  • Nfkbia protein, mouse
  • Nfkbia protein, rat
  • Tumor Necrosis Factor-alpha
  • NF-KappaB Inhibitor alpha
  • Calcimycin
  • p-Methoxy-N-methylphenethylamine
  • p38 Mitogen-Activated Protein Kinases
  • Tetradecanoylphorbol Acetate
  • Calcium