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Anti-inflammatory effect of torilidis fructus ethanol extract through inhibition of Src
Authors:Gyubyung Park  Eunji Kim  Young-Jin Son  Deok Hyo Yoon  Gi-Ho Sung  Adithan Aravinthan
Affiliation:1. Gyeonggi Science High School for the Gifted, Suwon, Republic of Korea;2. Department of Genetic Engineering, Sungkyunkwan University, Suwon, Republic of Korea;3. Department of Pharmacy, Sunchon National University, Suncheon, Korea;4. Institute for Bio-Medical Convergence, International St. Mary's Hospital and College of Medicine, Catholic Kwandong University Incheon, Incheon, Republic of Korea;5. College of Veterinary Medicine, Chonbuk National University, Iksan, Republic of Korea
Abstract:
Context: Torilidis fructus, fruits of Torilis japonica Decadolle (Umbelliferae), is a medicinal herb traditionally used as a pesticide, an astrictive, or a medicine for various inflammatory diseases.

Objectives: Due to the lack of pharmacological studies on this herbal medicine, we explored the inhibitory activity of torilidis fructus on the macrophage-mediated inflammatory response using its ethanol extract (Tf-EE).

Material and methods: The Griess assay and prostaglandin (PGE2) ELISA assay were conducted with Tf-EE (0-75?µg/mL) and LPS (1?µg/mL) treated RAW264.7 cells in cultured media. Tf-EE pretreated RAW264.7 cells were incubated with LPS for 6?h and semi-quantitative PCR was performed. Reporter gene assays, overexpression of target enzymes and immunoblotting were performed on macrophages to determine the molecular targets of Tf-EE.

Results: Tf-EE markedly suppressed the inflammatory response of macrophages, such as lipopolysaccharide (LPS)-induced nitric oxide (NO) and PGE2 production with IC50 values of 35.66 and 62.47?µg/mL, respectively. It was also found that Tf-EE reduced the expression of inducible NO synthase (iNOS) and cyclooxygenase (COX)-2 by 80%. Nuclear translocation and activation of nuclear factor (NF)-κB (p65 and p50) were declined by 60% and 30% respectively, and their regulatory events including the phosphorylation of AKT, IκBα, Src, and the formation of complexes between Src and p-p85 were also recognized to be diminished.

Conclusions: The signalling events managed by Src and p85 complex seemed to be critically involved in Tf-EE-mediated anti-inflammatory response. This might suggest that Tf-EE exhibited anti-inflammatory effects through Src-targeted inhibition of NF-κB.
Keywords:Inflammatory mediators  NF-κB  nitric oxide  macrophages
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