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Effect of alpha-pinene on nuclear translocation of NF-kappa B in THP-1 cells

Acta Pharmacol Sin. 2004 Apr;25(4):480-4.

Abstract

Aim: To study the effects of alpha-pinene on nuclear translocation of nuclear factor-kappa B (NF-kappa B) and the expression of the inhibitor of NF-kappa B (I kappa B alpha) in human monocyte THP-1 cell line.

Methods: THP-1 cells were incubated with alpha-pinene (1, 10, and 100 mg/L, for 30 min) before being stimulated with lipopolysaccharide (LPS, 1 mg/L, 30 min). The location of NF-kappa B p65 subunit (NF-kappa B/p65) in THP-1 cells was detected by immunofluorescence and laser scanning confocal microscope (LSCM). The expression of NF-kappa B/p65 in nuclei and that of I kappa B alpha in cytoplasm were measured by Western-blot analysis.

Results: The majority of FITC-labelled NF-kappa B/p65 was located in the nuclei being stimulated with LPS. Whereas, no such fluorescence was seen in the nuclei of the groups pretreated with alpha-pinene or control cells. alpha-Pinene pretreatment decreased the NF-kappa B/p65 nuclear translocation in LPS-stimulated THP-1 cells, and this effect was dose-dependent, but there was no reaction in LPS-unstimulated THP-1 cells. alpha-Pinene pretreatment increased I kappa B alpha protein level in cytoplasm, compared with that in LPS-stimulated THP-1 cells.

Conclusion: In a dose-related fashion, alpha-pinene inhibits the nuclear translocation of NF-kappa B induced by LPS in THP-1 cells, and this effect is partly due to the upregulation of I kappa B alpha expression.

MeSH terms

  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology*
  • Bicyclic Monoterpenes
  • Cell Nucleus / metabolism
  • Cytoplasm / metabolism
  • Dose-Response Relationship, Drug
  • Eucalyptus / chemistry
  • Humans
  • I-kappa B Proteins / metabolism*
  • Leukemia, Myeloid / metabolism
  • Leukemia, Myeloid / pathology
  • Monoterpenes / isolation & purification
  • Monoterpenes / pharmacology*
  • NF-KappaB Inhibitor alpha
  • NF-kappa B / metabolism*
  • Plants, Medicinal / chemistry
  • Protein Transport
  • Transcription Factor RelA
  • Tumor Cells, Cultured
  • Up-Regulation

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Bicyclic Monoterpenes
  • I-kappa B Proteins
  • Monoterpenes
  • NF-kappa B
  • NFKBIA protein, human
  • Transcription Factor RelA
  • NF-KappaB Inhibitor alpha
  • alpha-pinene