Epimagnolin A inhibits IL-6 production by inhibiting p38/NF-κB and AP-1 signaling pathways in PMA-stimulated THP-1 cells.
Hyun-Woo ChunSoo-Jin KimThu-Huyen PhamYesol BakJaewook OhHyung-Won RyuSei-Ryang OhJin-Tae HongDo-Young YoonPublished in: Environmental toxicology (2019)
Epimagnolin A is a lignan obtained from the flower buds of Magnolia fargesii, which is traditionally used in Asian medicine for treating headache and nasal congestion. A herbal compound fargesin obtained from M. fargesii, has exerted anti-inflammatory effects in human monocytic THP-1 cells in the previous study. The anti-inflammatory effects of epimagnolin A, however, have been not elucidated yet. In this study, it was demonstrated that epimagnolin A reduced phorbol-12-myristate-13-acetate (PMA)-induced IL-6 promoter activity and IL-6 production in human monocytic THP-1 cells. Furthermore, it was investigated the modulating effects of epimagnolin A on mitogen-activated protein kinase, nuclear factor-kappa B (NF-κB), and activator protein 1 (AP-1) activities. Phosphorylation of p38 and nuclear translocation of p50 and c-Jun were down-regulated by epimagnolin A in the PMA-stimulated THP-1 cell. The results revealed that epimagnolin A attenuated the binding affinity of NF-κB and AP-1 transcription factors to IL-6 promoter and IL-6 production through p38/NF-kB and AP-1 signaling pathways in the PMA-stimulated THP-1 cells. These results suggest that epimagnolin A can be a useful drug for the treatment of inflammatory diseases.
Keyphrases
- nuclear factor
- signaling pathway
- induced apoptosis
- transcription factor
- pi k akt
- cell cycle arrest
- oxidative stress
- toll like receptor
- endoplasmic reticulum stress
- lps induced
- endothelial cells
- dna methylation
- gene expression
- stem cells
- cell death
- anti inflammatory
- cell proliferation
- protein kinase
- binding protein
- high speed
- atomic force microscopy
- tyrosine kinase
- genome wide identification