The effects of diallyl sulfide upon Porphyromonas gingivalis lipopolysaccharide stimulated proinflammatory cytokine expressions and nuclear factor-kappa B activation in human gingival fibroblasts

J Periodontal Res. 2015 Jun;50(3):380-8. doi: 10.1111/jre.12217. Epub 2014 Sep 9.

Abstract

Background and objective: Diallyl sulfide (DAS), a flavor compound from garlic, has varied potential therapeutic activities. Periodontitis is a disease that develops because of host-mediated inflammation to periodontal pathogens. In this study, the effects of DAS on the common proinflammatory cytokines and nuclear factor-kappa B (NF-κB) in human gingival fibroblasts (HGFs) being stimulated with lipopolysaccharide from Porphyromonas gingivalis, a potent periodontal pathogen, were evaluated.

Material and methods: Cytotoxicities of DAS and lipopolysaccharide on HGFs were measured with MTS assay. The mRNA and protein expressions of proinflammatory cytokines, including interleukin (IL)-1β, IL-6 and tumor necrosis factor (TNF)-α, from the HGFs treated with lipopolysaccharide with and without DAS were examined with reverse transcription-polymerase chain reaction and immunocytochemistry, respectively. In addition, the activation and nuclear translocation of NF-κB with and without DAS were compared.

Results: DAS and lipopolysaccharide treatments within 3 mm and 10 μg/mL, respectively, did not affect the survival rate of HGFs. Lipopolysaccharide (1 μg/mL) significantly increased the mRNA expressions of IL-1β, IL-6 and TNF-α; however, DAS (1 mm) inhibited these expressions. The protein expressions of TNF-α, IL-1β, as well as the NF-κB nuclear translocation were increased after lipopolysaccharide treatment, but decreased when there was a DAS pretreatment.

Conclusion: DAS diminished P. gingivalis lipopolysaccharide-stimulated cytokine expression and NF-κB activation in HGFs; we therefore suggest DAS may be beneficial on periodontal inflammation.

Keywords: cytokine; diallyl sulfide; gingiva; lipopolysaccharide; nuclear factor-kappa B.

Publication types

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

MeSH terms

  • Allyl Compounds / pharmacology*
  • Allyl Compounds / toxicity
  • Cell Culture Techniques
  • Cell Survival / drug effects
  • Cells, Cultured
  • Coloring Agents
  • Cytokines / drug effects*
  • Fibroblasts / drug effects*
  • Garlic*
  • Gingiva / cytology
  • Gingiva / drug effects*
  • Humans
  • Inflammation Mediators / analysis*
  • Interleukin-1beta / drug effects
  • Interleukin-6 / analysis
  • Lipopolysaccharides / pharmacology*
  • Lipopolysaccharides / toxicity
  • NF-kappa B / drug effects*
  • Plant Oils / pharmacology*
  • Plant Oils / toxicity
  • Porphyromonas gingivalis / physiology*
  • Sulfides / pharmacology*
  • Sulfides / toxicity
  • Tetrazolium Salts
  • Thiazoles
  • Tumor Necrosis Factor-alpha / drug effects

Substances

  • Allyl Compounds
  • Coloring Agents
  • Cytokines
  • IL6 protein, human
  • Inflammation Mediators
  • Interleukin-1beta
  • Interleukin-6
  • Lipopolysaccharides
  • NF-kappa B
  • Plant Oils
  • Sulfides
  • Tetrazolium Salts
  • Thiazoles
  • Tumor Necrosis Factor-alpha
  • 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium
  • allyl sulfide