Aucubin prevents steroid-induced osteoblast apoptosis by enhancing autophagy via AMPK activation

J Cell Mol Med. 2021 Nov;25(21):10175-10184. doi: 10.1111/jcmm.16954. Epub 2021 Oct 6.

Abstract

Steroid-induced osteoblast apoptosis is a crucial pathological process in steroid-induced osteonecrosis of the femoral head (SONFH). Autophagy can resist apoptosis and AMPK plays an important role in autophagy regulation. Aucubin from the small tree Eucommia ulmoides Oliv., which has a long history of use in orthopaedics and traumatology in Asian medicine, can promote bone formation, but whether it can slow or prevent steroid-osteoblast apoptosis is unclear. Therefore, we investigated the pathogenesis of SONFH and how the osteoblast responds to aucubin under the dexamethasone stimulation. In human femoral head osteonecrosis specimens, we found that the autophage and apoptosis level were increased, and the AMPK signalling was crucial to autophagy. We observed that aucubin could prevent dexamethasone-induced apoptosis in osteoblasts by enhancing the level of autophagy. Further, we confirmed that the regulatory effect of aucubin on autophagy and apoptosis was achieved by activating AMPK signalling. We have demonstrated a mechanism of disease progression and shown that aucubin could enhance autophagy through AMPK signalling to prevent osteoblast apoptosis. These findings provide a basis for the further investigation of the potential therapeutic role of aucubin in the SONFH.

Keywords: SONFH; apoptosis; aucubin; autophagy; osteoblast; steroid.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AMP-Activated Protein Kinases / genetics
  • AMP-Activated Protein Kinases / metabolism*
  • Animals
  • Apoptosis / drug effects
  • Autophagy / drug effects*
  • Cell Line
  • Dose-Response Relationship, Drug
  • Humans
  • Immunophenotyping
  • Iridoid Glucosides / pharmacology*
  • Mice
  • Osteoblasts / drug effects*
  • Osteoblasts / metabolism*
  • Osteoblasts / ultrastructure
  • Phosphorylation
  • Protective Agents / pharmacology*
  • Steroids / pharmacology*

Substances

  • Iridoid Glucosides
  • Protective Agents
  • Steroids
  • aucubin
  • AMP-Activated Protein Kinases