Effect of osthol on apoptosis and bone resorption of osteoclasts cultured in vitro.
- Author:
Lei-Guo MING
1
;
Ming-Gang WANG
;
Ke-Ming CHEN
;
Jian ZHOU
;
Gui-Qiu HAN
;
Rui-Qing ZHU
Author Information
1. College of Life Science and Engineering, Lanzhou University of Technology, Lanzhou, China.
- Publication Type:Journal Article
- MeSH:
Acid Phosphatase;
metabolism;
Animals;
Apoptosis;
drug effects;
Bone Resorption;
Cells, Cultured;
Cnidium;
chemistry;
Coumarins;
isolation & purification;
pharmacology;
Gene Expression;
Isoenzymes;
metabolism;
Mitogen-Activated Protein Kinase 8;
metabolism;
Mitogen-Activated Protein Kinase 9;
metabolism;
Osteoclasts;
metabolism;
pathology;
Osteoprotegerin;
metabolism;
Phosphorylation;
Plants, Medicinal;
chemistry;
RANK Ligand;
metabolism;
Rabbits;
Seeds;
chemistry;
Signal Transduction;
Tartrate-Resistant Acid Phosphatase
- From:
Acta Pharmaceutica Sinica
2012;47(2):174-179
- CountryChina
- Language:Chinese
-
Abstract:
This study is to investigate the effect of osthol on osteoclasts' activity, bone resorption as well as apoptosis in vitro, and explore the mechanism of osthol in preventing osteoporosis. Osteoclasts were separated from long-limb bones of new born rabbits, cultured in 24-well plate with glass slices and bone slices, and treated by 1 x 10(-5) mol x L(-1) osthol. Osteoclasts were identified by observing live cells with phase contrast microscope, HE staining, TRAP staining and toluidine blue staining of bone resorption pits. The numbers of bone resorption pits were counted as well as the surface area of bone resorption on bone slice. Osteoclasts were stained with acridine orange to detect the cell apoptosis. The ratio of apoptotic osteoclasts was observed under fluorescence microscope. The gene expression of RANKL, OPG, TRAP and p-JNK1/2 protein expression were examined using real time PCR and Western blotting, respectively. Comparing with the control group without osthol, the rates of apoptotic osteoclasts increased obviously and the number and area of bone resorption pits decreased evidently with 1 x 10(-5) mol x L(-1) osthol. There is significant difference between control group and experiment group treated by 1 x 10(-5) mol x L(-1) osthol. Therefore, the osthol through RANK+RANKL/TRAF6/Mkk/JNK signal pathway inhibits the osteoclasts activity, enhances osteoclasts apoptotic and inhibits the bone resorption.
