4'-Hydroxywogonin suppresses lipopolysaccharide-induced inflammatory responses in RAW 264.7 macrophages and acute lung injury mice

PLoS One. 2017 Aug 8;12(8):e0181191. doi: 10.1371/journal.pone.0181191. eCollection 2017.

Abstract

4'-Hydroxywogonin (4'-HW), a flavonoid, has been isolated from various plants and shown to inhibit NO production in macrophages. However, the molecular mechanisms and its in vivo activity have not been determined. Our study aimed to investigate the mechanisms underlying the anti-inflammatory effects of 4'-HW in vitro and in vivo. We showed that 4'-HW potently reduced the expression levels of COX-2 and iNOS as well as their products, prostaglandin E2 (PGE2) and nitric oxide (NO) respectively, in LPS-stimulated RAW 264.7 macrophages. 4'-HW also suppressed LPS-induced pro-inflammatory cytokines at mRNA and protein levels. Moreover, 4'-HW blocked the interaction of TAK1 and TAB1 in LPS-stimulated RAW 264.7 macrophages, resulting in an inhibition of the TAK1/IKK/NF-κB signaling pathway. Furthermore, 4'-HW also reduced the phosphorylation of MAPKs and PI3/Akt signaling pathways in LPS-stimulated RAW 264.7 macrophages. 4'-HW was also significantly decreased the intracellular reactive oxygen species (ROS) level. The effect of 4'-HW was confirmed in vivo. 4'-HW exhibited potent protective effect against LPS-induced ALI in mice. These findings indicate that 4'-HW suppresses the LPS-induced response in vitro and in vivo. It is likely that the inhibition of the TAK1/IKK/NF-κB, MAPKs and PI3/AKT signaling pathways contribute to the anti-inflammatory effects of 4'-HW. Our study suggests that 4'-HW may be an important functional constituent in the plants and has the potential value to be developed as a novel anti-inflammatory agent.

MeSH terms

  • Acute Lung Injury / drug therapy*
  • Acute Lung Injury / immunology*
  • Animals
  • Anti-Inflammatory Agents / pharmacology*
  • Cell Line
  • Cyclooxygenase 2 / metabolism
  • Disease Models, Animal
  • Drug Evaluation, Preclinical
  • Flavanones / pharmacology*
  • Lipopolysaccharides
  • MAP Kinase Signaling System / drug effects
  • MAP Kinase Signaling System / physiology
  • Macrophages / drug effects*
  • Macrophages / immunology*
  • Male
  • Mice, Inbred C57BL
  • NF-kappa B / metabolism
  • Nitric Oxide Synthase Type II / metabolism
  • Proto-Oncogene Proteins c-akt / metabolism
  • Reactive Oxygen Species / metabolism
  • Toll-Like Receptor 4 / metabolism

Substances

  • 4'-hydroxywogonin
  • Anti-Inflammatory Agents
  • Flavanones
  • Lipopolysaccharides
  • NF-kappa B
  • Reactive Oxygen Species
  • Tlr4 protein, mouse
  • Toll-Like Receptor 4
  • Nitric Oxide Synthase Type II
  • Nos2 protein, mouse
  • Ptgs2 protein, mouse
  • Cyclooxygenase 2
  • Proto-Oncogene Proteins c-akt

Grants and funding

This work was supported by grants from the National Science Foundation of China (Grant 81402806 to Dr. Yan Zhang and Grant 31470865 to Dr. Richard D Ye). This work was also supported by the Science and Technology Development Fund (FDCT 026/2016/A1) and the funds from the University of Macau (CPG2015-00018-ICMS and SRG2015-00047-ICMS-QRCM) to Dr Richard D Ye.