4.6 Article

Dysiarenone from Marine Sponge Dysidea arenaria Attenuates ROS and Inflammation via Inhibition of 5-LOX/NF-κB/MAPKs and Upregulation of Nrf-2/OH-1 in RAW 264.7 Macrophages

Journal

JOURNAL OF INFLAMMATION RESEARCH
Volume 14, Issue -, Pages 587-597

Publisher

DOVE MEDICAL PRESS LTD
DOI: 10.2147/JIR.S283745

Keywords

dysiarenone; Dysidea arenaria; Nrf2; HO-1; NF-kappa B

Categories

Funding

  1. Natural Science Foundation of China [81973915, 81773978, 82004046]
  2. Guangdong Basic and Applied Basic Research Foundation [2019A1515010391, 2020A1515010592]
  3. Shenzhen Innovation of Science and Technology Commission [LGKCZSYS2019000046, JCYJ20170412103841386, LGKCYLWS2019000864]
  4. Shenzhen Key Medical Discipline Construction Fund [SZXK039]

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Our study demonstrated that dysiarenone possesses anti-inflammatory and anti-oxidative activities by inhibiting the 5-LOX/NF-κB/MAPK and Nrf2/HO-1 signaling pathways. Dysiarenone shows potential as a promising lead compound for inflammatory diseases.
Background: Marine natural products harbor a variety of pharmacological activities, and the sea species have been becoming a main source of new drug candidate. In pursuit of safer and more effective anti-inflammation drug, the anti-inflammatory activities, anti-oxygenation effects and underlying molecular mechanisms of compound dysiarenone from Dysidea arenaria were investigated via LPS-induced RAW 264.7 cell model. Methods: Firstly, RAW 264.7 cells have been stimulated with LPS and treated with dysiarenone, and the cell viability of the LPS-treated RAW 264.7 cells was examined. One-step method, DCFH-DA fluorescence probe method was used to detect reactive oxygen species (ROS). The modulation of dysiarenone on anti-inflammation was detected by enzyme-linked immunosorbent assay by measuring the release of inflammatory cytokines (TNF-alpha and IL-6), and inflammatory mediators (LTB4). Further, the underlying anti-inflammatory mechanism of dysiarenone was explored by determining the expression of inducible 5-LOX, MAPKs, p-Akt, and p-NF-kappa B p65. Oxidative stress is tightly connected with inflammation, which was also evaluated through nuclear factor erythroid 2-related factor 2 (Nrf2)/heme oxygenase-1 (OH-1) signaling pathway. Results: Our study unraveled that dysiarenone between 2 and 8 mu M reduces the inflammation responses via suppressing the production of inflammatory cytokines (TNF-alpha and IL-6) and inflammatory mediators (LTB4). Dysiarenone down-regulated the protein levels of inducible 5-LOX via the inhibition of phosphorylation of MAPKs (including p38, ERK), Akt and NF-kappa B p65. Additionally, dysiarenone decreases ROS accumulation by upregulating HO-1 expression via nuclear translocation of Nrf2. Conclusion: In conclusion, we demonstrated that dysiarenone possesses anti-inflammation and anti-oxidation activity via inhibiting 5-LOX/NF-kappa B/MAPK and Nrf2/HO-1 signaling pathway. Dysiarenone might be a promising lead compound for inflammatory diseases.

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