Effect of Cone of Pinus densiflora on DNCB-Induced Allergic Contact Dermatitis-Like Skin Lesion in Balb/c Mice

Nutrients. 2021 Mar 4;13(3):839. doi: 10.3390/nu13030839.

Abstract

Cone of Pinus densiflora (CP), or Korean red pinecone, is a cluster of Pinus densiflora fruit. CP has also been verified in several studies to have anti-oxidation, anti-fungal, anti-bacterial, and anti-melanogenic effects. However, anti-inflammatory effects have not yet been confirmed in the inflammatory responses of pinecones to allergic contact dermatitis. The purpose of this study is to prove the anti-inflammatory effect of CP on allergic contact dermatitis (ACD) in vitro and in vivo. CP inhibited the expression of TSLP, TARC, MCP-1, TNF-α, and IL-6 in TNF-α/IFN-γ-stimulated HaCaT cells and MCP-1, GM-CSF, TNF-α, IL-6, and IL-8 in PMACI (phorbol-12-myristate-13-acetate plus A23187)-stimulated HMC-1 cells. CP inhibited the phosphorylation of mitogen-activated protein kinase (MAPKs), as well as the translocation of NF-κB on TNF-α/IFN-γ stimulated in HaCaT cells. In vivo, CP decreased major symptoms of ACD, levels of IL-6 in skin lesion, thickening of the epidermis and dermis, infiltration of eosinophils and mast cells, and the infiltration of CD4+ T cells and CD8+ T cells. This result suggests that CP represents a potential alternative medicine to ACD for diseases such as chronic skin inflammation.

Keywords: Cone of Pinus densiflora; HMC-1; HaCaT; MAPK; MCP-1; NF-κB; TARC; allergic contact dermatitis.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / pharmacology*
  • Biological Transport / drug effects
  • Dermatitis, Allergic Contact / drug therapy*
  • Dermatitis, Allergic Contact / etiology
  • Dinitrochlorobenzene
  • Disease Models, Animal
  • Eosinophils / drug effects
  • Epidermis / drug effects
  • HaCaT Cells
  • Humans
  • Interferon-gamma / metabolism
  • Mast Cells / drug effects
  • Mice
  • Mice, Inbred BALB C
  • Mitogen-Activated Protein Kinases / metabolism
  • NF-kappa B / metabolism
  • Phosphorylation / drug effects
  • Pinus / chemistry*
  • Plant Extracts / pharmacology*
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Anti-Inflammatory Agents
  • Dinitrochlorobenzene
  • NF-kappa B
  • Plant Extracts
  • Tumor Necrosis Factor-alpha
  • Interferon-gamma
  • Mitogen-Activated Protein Kinases