Neuroinflammation and Acetylcholinesterase Inhibitory Potentials of a Spiroketal-Enol Ether Polyyne Isolated from Artemisia pallens Wall. ex DC

Chem Biodivers. 2024 Mar;21(3):e202301762. doi: 10.1002/cbdv.202301762. Epub 2024 Feb 15.

Abstract

Artemisia pallens Wall. ex DC (Asteraceae) is cultivated for the production of high-value essential oil from its aerial biomass. In this study, the chemical composition of the root (crop-residue) essential oil was investigated for the first time, using column-chromatography, GC-FID, GC-MS, LC-QTOF, and NMR techniques, which led to the identification of twenty constituents, with isolation of (E)-2-(2',4'-hexadiynylidene)-1,6-dioxaspiro [4.5]dec-3-ene (D6). The D6 was evaluated in vitro for neuroinflammation and acetylcholinesterase inhibitory potential. It showed inhibition of neuroinflammation in a concentration-dependent manner with significant inhibition of pro-inflammatory cytokines (TNF-α and IL-6) in LPS-stimulated BV2 microglial cells. D6 did not have any significant effect on the viability of the cells at the therapeutic concentrations. D6 also has shown acetylcholinesterase inhibitory potential (51.90±1.19 %) at the concentration of log 106 nM. The results showed that D6 has a potential role in the resolution of neuroinflammation, and its acetylcholinesterase inhibitory potential directs further investigation of its role in the management of Alzheimer's disease-related pathogenesis.

Keywords: Artemisia pallens; anti-neuroinflammation; antiacetylcholinesterase; spiroketal-enol ether diacetylene.

MeSH terms

  • Acetylcholinesterase
  • Artemisia* / chemistry
  • Ether
  • Furans*
  • Neuroinflammatory Diseases
  • Oils, Volatile* / chemistry
  • Polyynes
  • Spiro Compounds*

Substances

  • Acetylcholinesterase
  • Ether
  • spiroketal
  • Polyynes
  • Oils, Volatile
  • Furans
  • Spiro Compounds