Suppression of lipopolysaccharide-induced COX-2 expression via p38MAPK, JNK, and C/EBPβ phosphorylation inhibition by furomagydarin A, a benzofuran glycoside from Magydaris pastinacea

Shiu Wen Huang, Ming Jen Hsu, Hsiu Chen Chen, Rita Meleddu, Simona Distinto, Elias Maccioni, Filippo Cottiglia

Research output: Contribution to journalArticlepeer-review

Abstract

The phytochemical investigation of the methanol extract of the seeds of Magydaris pastinacea afforded two undescribed benzofuran glycosides, furomagydarins A-B (1, 2), together with three known coumarins. The structures of the new isolates were elucidated after extensive 1D and 2D NMR experiments as well as HR MS. Compound 1 was able to inhibit the COX-2 expression in RAW264.7 macrophages exposed to lipopolysaccharide, a pro-inflammatory stimulus. RT-qPCR and luciferase reporter assays suggested that compound 1 reduces COX-2 expression at the transcriptional level. Further studies highlighted the capability of compound 1 to suppress the LPS-induced p38MAPK, JNK, and C/EBPβ phosphorylation, leading to COX-2 down-regulation in RAW264.7 macrophages.

Original languageEnglish
Article number2287420
JournalJournal of Enzyme Inhibition and Medicinal Chemistry
Volume39
Issue number1
DOIs
Publication statusPublished - 2023

Keywords

  • benzofurans
  • C/EBPβ
  • COX-2
  • JNK
  • Magydaris pastinacea
  • p38MAPK

ASJC Scopus subject areas

  • Pharmacology
  • Drug Discovery

Fingerprint

Dive into the research topics of 'Suppression of lipopolysaccharide-induced COX-2 expression via p38MAPK, JNK, and C/EBPβ phosphorylation inhibition by furomagydarin A, a benzofuran glycoside from Magydaris pastinacea'. Together they form a unique fingerprint.

Cite this