Anti-inflammatory effect of Cortex Eucommiae via modulation of the toll-like receptor 4 pathway in lipopolysaccharide-stimulated RAW 264.7 macrophages

作者：Koh Wonil; Shin Joon Shik; Lee Jinho; Lee In Hee; Lee Sang Kook; Ha In Hyuk^*; Chung Hwa Jin

来源：Journal of Ethnopharmacology, 2017, 209: 255-263.

DOI：10.1016/j.jep.2017.08.001

• Cortex Eucommiae
• Anti-inflammatory
• RAW 264.7 cells
• TLR-4
• Myd88

Ethnopharmocological relevance: Cortex Eucommiae (CE), the bark of Eucommia ulmoides Oliv., has been traditionally used for its kidney-tonifying and bone- and tendon-enhancing properties in Korea, China, and Japan. CE has been historically prescribed for inflammatory conditions such as arthritis of the knee and ankle. Aim of the study: Although CE has recently been shown to suppress inflammation in scientific studies, whether this effect involves modulation of the toll-like receptor 4 (TLR-4) pathway is currently unknown.
Materials and methods: The modulatory effect of CE on the TLR-4 pathway, both myeloid differentiation primary response gene 88 (Myd88)-dependent and independent, was investigated through real-time reverse transcriptase-polymerase chain reaction (RT-PCR), western blotting, and a reporter gene assay in lipopolysaccharide (LPS)-stimulated RAW 264.7 murine macrophages.
Results: CE dose-dependently inhibited nitric oxide production without significant cytotoxicity with an IC50 of 356.23 mu g/mL. In addition, CE down-regulated both LPS-induced mRNA and protein expression of inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2), tumor necrosis factor-alpha (INF-alpha), and interleultin-1 beta (IL-1 beta) in a dose-dependent manner. CE suppressed LPS-induced activation of nuclear factor-kappa B (NF-kappa B) and the mitogen-activated protein kinase (MAPK) pathways, which together comprise the Myd88-dependent TLR-4 pathway. The phosphoinositide 3-kinase (PI3K)/Akt/mammalian target of rapamycin (mTOR) pathway was also down-regulated by CE in a dose-dependent manner. CE additionally suppressed LPS-induced activation of interferon-beta (IFN-beta) and signal transducer and activator of transcription (STAT) pathway, which is associated with the Myd88-independent TLR-4 pathway.
Conclusions: CE down-regulated both Myd88-dependent and independent TLR-4 pathways, thus exerting anti-inflammatory effects. These results suggest that CE may be used as a potential therapeutic agent against chronic inflammatory diseases.

• 出版日期2017-9-14