Baicalin downregulates Porphyromonas gingivalis lipopolysaccharide-upregulated IL-6 and IL-8 expression in human oral keratinocytes by negative regulation of TLR signaling

PLoS One. 2012;7(12):e51008. doi: 10.1371/journal.pone.0051008. Epub 2012 Dec 11.

Abstract

Periodontal (gum) disease is one of the main global oral health burdens and severe periodontal disease (periodontitis) is a leading cause of tooth loss in adults globally. It also increases the risk of cardiovascular disease and diabetes mellitus. Porphyromonas gingivalis lipopolysaccharide (LPS) is a key virulent attribute that significantly contributes to periodontal pathogenesis. Baicalin is a flavonoid from Scutellaria radix, an herb commonly used in traditional Chinese medicine for treating inflammatory diseases. The present study examined the modulatory effect of baicalin on P. gingivalis LPS-induced expression of IL-6 and IL-8 in human oral keratinocytes (HOKs). Cells were pre-treated with baicalin (0-80 µM) for 24 h, and subsequently treated with P. gingivalis LPS at 10 µg/ml with or without baicalin for 3 h. IL-6 and IL-8 transcripts and proteins were detected by real-time polymerase chain reaction and enzyme-linked immunosorbent assay, respectively. The expression of nuclear factor-κB (NF-κB), p38 mitogen-activated protein kinase (MAPK) and c-Jun N-terminal kinase (JNK) proteins was analyzed by western blot. A panel of genes related to toll-like receptor (TLR) signaling was examined by PCR array. We found that baicalin significantly downregulated P. gingivalis LPS-stimulated expression of IL-6 and IL-8, and inhibited P. gingivalis LPS-activated NF-κB, p38 MAPK and JNK. Furthermore, baicalin markedly downregulated P. gingivalis LPS-induced expression of genes associated with TLR signaling. In conclusion, the present study shows that baicalin may significantly downregulate P. gingivalis LPS-upregulated expression of IL-6 and IL-8 in HOKs via negative regulation of TLR signaling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology
  • Cells, Cultured
  • Down-Regulation / drug effects
  • Flavonoids / pharmacology*
  • Humans
  • Inflammation / metabolism
  • Interleukin-6 / biosynthesis*
  • Interleukin-8 / biosynthesis*
  • JNK Mitogen-Activated Protein Kinases / metabolism
  • Keratinocytes / metabolism*
  • Lipopolysaccharides
  • Mouth / pathology
  • Periodontitis / metabolism
  • Periodontitis / microbiology
  • Periodontitis / pathology
  • Phosphorylation
  • Porphyromonas gingivalis / chemistry
  • Porphyromonas gingivalis / pathogenicity
  • Scutellaria
  • Signal Transduction / drug effects
  • Toll-Like Receptors / biosynthesis*

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Flavonoids
  • Interleukin-6
  • Interleukin-8
  • Lipopolysaccharides
  • Toll-Like Receptors
  • baicalin
  • JNK Mitogen-Activated Protein Kinases

Grants and funding

This study was supported by the Hong Kong Research Grants Council (HKU766909M and HKU768411M to LJJ), and the Modern Dental Laboratory/HKU Endowment Fund to LJJ. The funders had no role in study design, data collection and analysis, decision to publish or preparation of the manuscript.