Anti-inflammatory activity of isobutylamides from zanthoxylum nitidum var. tomentosum

Fitoterapia. 2020 Apr:142:104486. doi: 10.1016/j.fitote.2020.104486. Epub 2020 Jan 24.

Abstract

Inflammation is a very common and important basic pathological process. There is still a great need for the isolation of effective anti-inflammatory agents from plants. In this paper, five new isobutylamides, zanthoxylumamides E-I (1-5), and four known isobutylamides (6-9) were isolated from Zanthoxylum nitidum var. tomentosum (Rutaceae). Chiral resolution of seven racemic isobutylamides (1-4 and 6-8) was successfully performed, and the absolute configurations of two stereoisomers of 1-4 were validated by ECD and NMR. The obtained isobutylamides were evaluated in vitro anti-inflammatory activity with the lipopolysaccharide (LPS)-stimulated production of nitric oxide (NO) in murine macrophage RAW264.7 cells. Compound 8 exhibited significant inhibition of LPS-induced NO production. The underlying molecular mechanisms of the anti-inflammatory activity of 8 revealed that it suppressed the NO production through the modulation of myeloid differentiation factor 88 (MyD88) and interferon regulatory factor 3 (IRF3) signaling pathways.

Keywords: Anti-inflammatory activities; Isobutylamides; RAW264.7 cells; Zanthoxylum nitidum var. tomentosum (Rutaceae); Zanthoxylumamides.

MeSH terms

  • Amides / chemistry
  • Amides / pharmacology*
  • Animals
  • Cell Survival
  • Inflammation / chemically induced*
  • Inflammation / drug therapy*
  • Lipopolysaccharides / toxicity
  • Mice
  • Models, Molecular
  • Molecular Structure
  • Nitric Oxide / metabolism
  • RAW 264.7 Cells
  • Zanthoxylum / chemistry*

Substances

  • Amides
  • Lipopolysaccharides
  • Nitric Oxide