[Effect of naringin on osteoclast differentiation]

Zhongguo Zhong Yao Za Zhi. 2015 Jan;40(2):308-12.
[Article in Chinese]

Abstract

Objective: To discuss the effect of Drynariae Rhizoma's naringin on osteoclasts induced by mouse monocyte RAW264.7.

Method: RAW264.7 cells were induced by 100 μg x L(-1) nuclear factor-κB receptor activator ligand (RANKL) and became mature osteoclasts, which were identified through TRAP specific staining and bone resorption. MTT method was sued to screen and inhibit and the highest concentration of osteoclasts. After being cultured with the screened medium containing naringin for 5 days, positive TRAP cell counting and bone absorption area analysis were adopted to observe the effect of naringin on the formation of osteoclast sells and the bone absorption function. The osteoclast proliferation was measured by flow cytometry. The effects of RANK, TRAP, MMP-9, NFATc1 and C-fos mRNA expressions on nuclear factor-κB were detected by RT-PCR.

Result: Naringin could inhibit osteoclast differentiation, bone absorption function and proliferation activity of osteoclasts, significantly down-regulate RANK, TRAP, MMP-9 and NFATc1 mRNA expressions in the osteoclast differentiation process, and up-regulate the C-fos mRNA expression.

Conclusion: Naringin could inhibit osteoclast differentiation, proliferation and bone absorption function. Its mechanism may be achieved by inhibiting the specific gene expression during the osteoclast differentiation process.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acid Phosphatase / metabolism
  • Animals
  • Cell Differentiation / drug effects
  • Cell Proliferation / drug effects
  • Cells, Cultured
  • Flavanones / pharmacology*
  • Isoenzymes / metabolism
  • Matrix Metalloproteinase 9 / genetics
  • Mice
  • NFATC Transcription Factors / genetics
  • Osteoclasts / cytology
  • Osteoclasts / drug effects*
  • Tartrate-Resistant Acid Phosphatase

Substances

  • Flavanones
  • Isoenzymes
  • NFATC Transcription Factors
  • Nfatc1 protein, mouse
  • Acid Phosphatase
  • Acp5 protein, mouse
  • Tartrate-Resistant Acid Phosphatase
  • Matrix Metalloproteinase 9
  • naringin