4.7 Article

Investigation of Active Anti-Inflammatory Constituents of Essential Oil from Pinus koraiensis (Sieb. et Zucc.) Wood in LPS-Stimulated RBL-2H3 Cells

Journal

BIOMOLECULES
Volume 11, Issue 6, Pages -

Publisher

MDPI
DOI: 10.3390/biom11060817

Keywords

Pinus koraiensis; essential oil; anti-inflammatory; active compound; alpha-pinene; beta-pinene; alpha-terpineol; longifolene

Funding

  1. National Institute of Forest Science [FP0700-2015-02]
  2. National Institute of Forest Science (NIFOS), Republic of South Korea [FP0700-2015-02] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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This study demonstrated the anti-inflammatory activity of essential oil extracted from Korean pine wood and identified key anti-inflammatory constituents. These constituents showed potential for the management and treatment of inflammatory conditions, indicating possible development of novel anti-inflammatory drugs.
In a previous study, we demonstrated the anti-inflammatory activity of the essential oil extracted from Korean pine (Pinus koraiensis, Sieb. et Zucc.) wood. This study aims to investigate the active anti-inflammatory constituents of P. koraiensis oil. The essential oil was extracted from P. koraiensis wood by hydrodistillation and was divided into six fractions (A-F) through fractional distillation. Then, the anti-inflammatory activities of the fractions (A-F) were determined. Fractions A and F markedly downregulated the production of pro-inflammatory cytokines as well as the secretion of beta-hexosaminidase in lipopolysaccharide (LPS)-stimulated RBL-2H3 cells. The main constituents of the active anti-inflammatory A and F fractions were (+)-alpha-pinene, (-)-beta-pinene, (+)-alpha-terpineol, 3-carene, (+)-limonene, and longifolene. These six single compounds decreased the expression of inflammatory-related genes (i.e., IL-4 and IL-13) as well as the secretion of beta-hexosaminidase in LPS-stimulated RBL-2H3 cells. (+)-alpha-Pinene, (-)-beta-pinene, (+)-alpha-terpineol, and longifolene exhibited the strongest effects; these effects were comparable to those of the positive control (i.e., dexamethasone). The findings indicate that the interactions between these components exhibit potential for the management and/or treatment of inflammatory conditions as well as base structures for the development of novel anti-inflammatory drugs.

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