A 70% Ethanol Neorhodomela munita Extract Attenuates RANKL-Induced Osteoclast Activation and H2O2-Induced Osteoblast Apoptosis In Vitro

Molecules. 2024 Apr 11;29(8):1741. doi: 10.3390/molecules29081741.

Abstract

The rapid aging of the population worldwide presents a significant social and economic challenge, particularly due to osteoporotic fractures, primarily resulting from an imbalance between osteoclast-mediated bone resorption and osteoblast-mediated bone formation. While conventional therapies offer benefits, they also present limitations and a range of adverse effects. This study explores the protective impact of Neorhodomela munita ethanol extract (EN) on osteoporosis by modulating critical pathways in osteoclastogenesis and apoptosis. Raw264.7 cells and Saos-2 cells were used for in vitro osteoclast and osteoblast models, respectively. By utilizing various in vitro methods to detect osteoclast differentiation/activation and osteoblast death, it was demonstrated that the EN's potential to inhibit RANKL induced osteoclast formation and activation by targeting the MAPKs-NFATc1/c-Fos pathway and reducing H2O2-induced cell death through the downregulation of apoptotic signals. This study highlights the potential benefits of EN for osteoporosis and suggests that EN is a promising natural alternative to traditional treatments.

Keywords: in vitro osteoporosis; keyword ethanol extract of Neorhodomela munita; osteoblast; osteoclast.

MeSH terms

  • Animals
  • Apoptosis* / drug effects
  • Cell Differentiation / drug effects
  • Ethanol* / chemistry
  • Humans
  • Hydrogen Peroxide* / pharmacology
  • Mice
  • Osteoblasts* / drug effects
  • Osteoblasts* / metabolism
  • Osteoclasts* / drug effects
  • Osteoclasts* / metabolism
  • Osteogenesis / drug effects
  • Plant Extracts / chemistry
  • Plant Extracts / pharmacology
  • RANK Ligand* / metabolism
  • RAW 264.7 Cells
  • Signal Transduction / drug effects

Substances

  • Hydrogen Peroxide
  • RANK Ligand
  • Ethanol
  • Plant Extracts