Study of the Molecular Mechanism of Anti-inflammatory Activity of Bee venom in Lipopolysaccharide Stimulated RAW 264.7 Macrophages

  • PD Lam
  • PK Mandal
  • SY Hak
  • S-G Hwang
Keywords: Bee venom, Cyclooxygenase-2, Interleukin 1beta, Inducible nitric oxide synthase, Lipopolysaccharide, Macrophage, Mitogen activated protein kinase, Nuclear factor kappa-B.

Abstract

Purpose: Bee venom (BV) is traditionally used in many inflammatory chronic conditions but its mechanism of action at molecular level is not fully understood. This study was undertaken to elucidate the mechanism of action of bee venom at the molecular level Methods: We used lipopolysaccharide (LPS) stimulation in Raw 264.7 macrophage (RM) cells and studied the effect of BV on cell proliferation, inflammation related protein expression by western blotting and RNA expression by reverse transcriptase polymerase chain reaction (RT-PCR). Results: Bee venom was toxic to RM cells above10 μg/ml but reduced the production of nitric oxide (NO) at 2–10 μg/ml in LPS stimulated RM cells by inhibiting the expression of inducible nitric oxide synthase (iNOS) and cyclooxigenase (COX)-2 via nuclear factor (NF)-κB. However, bee venom also induced the pro-inflammatory cytokine, interleukin (IL)-1β via p38 mitogen activated protein kinase (MAPK) which is known to stimulate inflammatory activity.
Conclusion: It seems that NFκB and p38 MAPK signal pathways are  involved in triggering the functional activation of LPS-stimulated macrophage. We suggest that some components of bee venom can cause inflammation by inducing IL-1β via p38 MAPK while others act as anti-inflammatory by suppressing iNOS and COX2 via NFκB.

Keywords: Bee venom, Cyclooxygenase-2, Interleukin 1beta, Inducible nitric oxide synthase, Lipopolysaccharide, Macrophage, Mitogen activated protein kinase, Nuclear factor kappa-B.

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Articles

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eISSN: 1596-9827
print ISSN: 1596-5996