New oxindole alkaloids with selective osteoclast inhibitory activity from Gelsemium elegans

Nat Prod Res. 2022 May;36(10):2630-2636. doi: 10.1080/14786419.2021.1913589. Epub 2021 Apr 28.

Abstract

A new alkaloid 14-hydroxygelseziridine (1), along with four known oxindoles (2-5), was isolated and characterized from the well-known toxic medicine Gelsemium elegans. Their structures were elucidated by means of spectroscopic techniques and quantum chemistry calculations. Structurally, new compound 1 has a three membered oxygen ring at N-4/C-20. All compounds were tested for osteoclast (MOC-1) inhibitory activity in vitro. Compound 2 exhibited the selective osteoclast inhibitory activity. Flow cytometry revealed that the apoptosis of osteoclasts induced by 2. Furthermore, the PCR bioassay suggested that compound 2 may activate the apoptotic pathway of osteoclasts by reducing the expression of IL-6 and c-Jun, and increasing caspase 9. This work provided the evidence for the rationality as the traditional treatment for bone related diseases of G. elegans, and shed a new light on its further research.

Keywords: Gelsemium elegans; PCR bioassay; osteoclast inhibitory; oxindole alkaloids.

MeSH terms

  • Alkaloids* / chemistry
  • Alkaloids* / pharmacology
  • Gelsemium* / chemistry
  • Osteoclasts
  • Oxindoles / pharmacology

Substances

  • Alkaloids
  • Oxindoles