Bee venom suppresses LPS-mediated NO/iNOS induction through inhibition of PKC-alpha expression

J Ethnopharmacol. 2009 May 4;123(1):15-21. doi: 10.1016/j.jep.2009.02.044. Epub 2009 Mar 9.

Abstract

Ethnopharmacological relevance: Bee venom (BV) is a traditional Korean medicine that has been widely used with satisfactory results in the treatment of some immune-related diseases, especially rheumatoid arthritis.

Aim of the study: The purpose of this study is to elucidate the molecular mechanism underlying the anti-inflammatory effects of BV, which is used in the treatment of various inflammatory diseases in traditional Korean medicine. We evaluated the anti-inflammatory effect of BV on NO generation and iNOS expression by LPS in rat C6 glioma cells.

Material and methods: BV was obtained from the National Institute of Agricultural Science and Technology (NIAST) of Korea. Nitrite measurement, Immuno blot analysis, Reverse transcriptase-PCR and Electrophoretic mobility shift assay (EMSA) were used for assessment.

Results: BV suppressed the LPS-induced NO generation and iNOS expression, and it also inhibited the expressions of LPS-induced pro-inflammatory molecules including Cox-2 and IL-1 beta in rat C6 glioma cells. Then, BV inhibited LPS-induced expression of PKC-alpha and MEK/ERK, not p38 and JNK. Moreover, inhibition of LPS-induced iNOS expression by BV was dependent on transcriptional activities of AP-1/NF-kappaB through MEK/ERK pathway.

Conclusion: These results indicate that BV suppresses LPS-induced iNOS activation through regulation of PKC-alpha. Accordingly, BV exerts a potent suppressive effect on pro-inflammatory responses in rat C6 glioma cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bee Venoms / pharmacology*
  • Cell Line, Tumor
  • Electrophoretic Mobility Shift Assay
  • Enzyme Induction
  • Lipopolysaccharides / pharmacology*
  • Nitric Oxide / biosynthesis*
  • Nitric Oxide Synthase Type II / biosynthesis*
  • Protein Kinase C-alpha / antagonists & inhibitors*
  • Rats
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • Bee Venoms
  • Lipopolysaccharides
  • Nitric Oxide
  • Nitric Oxide Synthase Type II
  • Protein Kinase C-alpha