Anti-inflammatory bibenzyls from the stems of Dendrobium huoshanense via bioassay guided isolation

Nat Prod Res. 2020 Feb;34(4):563-566. doi: 10.1080/14786419.2018.1489394. Epub 2018 Nov 3.

Abstract

The stems of Dendrobium huoshanense have long been used to prevent various diseases, including inflammatory diseases. This study was aimed to explain the anti-inflammatory effect of D. huoshanense stems in LPS-induced RAW 264.7 macrophages and to discover potential anti-inflammatory compounds. Results exhibited that D. huoshanense stems ethanol extract could significantly inhibit LPS-induced production of NO, TNF-α and IL-1β. Based on bioassay guided strategy, four bibenzyls (1-4) were isolated from D. huoshanense stems for the first time. Anti-inflammatory assay showed 1-4 could remarkably inhibit the production of NO in LPS-induced macrophages. Moreover, quantitative RT-PCR analysis displayed that the mRNA levels of iNOs, TNF-α and IL-1β could also be significantly reduced by 1-4. These results suggested that D. huoshanense stems ethanol extract and bibenzyls 1-4 might be well developed as therapeutic agent to prevent inflammatory diseases.

Keywords: Dendrobium huoshanense; anti-inflammation; bibenzyls; bioassay guided; macrophages.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / isolation & purification*
  • Anti-Inflammatory Agents / pharmacology
  • Bibenzyls / isolation & purification*
  • Bibenzyls / pharmacology
  • Biological Assay / methods
  • Dendrobium / chemistry*
  • Ethanol
  • Interleukin-1beta / genetics
  • Lipopolysaccharides
  • Macrophages / cytology
  • Macrophages / drug effects*
  • Macrophages / metabolism
  • Mice
  • Nitric Oxide Synthase Type II / genetics
  • Plant Extracts / chemistry
  • Plant Extracts / pharmacology
  • RAW 264.7 Cells / cytology
  • RNA, Messenger / drug effects
  • Tumor Necrosis Factor-alpha / genetics

Substances

  • Anti-Inflammatory Agents
  • Bibenzyls
  • IL1B protein, human
  • Interleukin-1beta
  • Lipopolysaccharides
  • Plant Extracts
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • Ethanol
  • NOS2 protein, human
  • Nitric Oxide Synthase Type II