Inhibition of RANKL-induced osteoclastogenesis through the suppression of the ERK signaling pathway by astragaloside IV and attenuation of titanium-particle-induced osteolysis

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Abstract

Astragaloside IV (AS-IV) is a natural plant extract that enhances osteoblast activity, and therefore, has the potential to treat osteoclast-related diseases. Such diseases include osteoporosis, periodontal disease, rheumatoid arthritis and aseptic prosthesis loosening. However, data associating the effects of AS-IV on osteoclasts are limited. The aim of the present study was to assess the effect of AS-IV on osteoclasts in vitro and in vivo. The in vitro studies demonstrated that AS-IV exerts potent inhibitory effects on the ligand of the receptor activator of nuclear factor-κB-induced osteoclastogenesis and revealed the mechanism of action of AS-IV, which inhibited osteoclastogenesis by suppression of the extracellular signal-regulated kinase signaling pathway. The in vivo studies proved that AS-IV attenuated titanium particle-induced osteolysis in a mouse calvarial model. Collectively, the findings of the study suggest that AS-IV is a potential natural agent for the treatment of osteoclast-related diseases.

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Li, M., Wang, W., Geng, L., Qin, Y., Dong, W., Zhang, X., … Zhang, M. (2015). Inhibition of RANKL-induced osteoclastogenesis through the suppression of the ERK signaling pathway by astragaloside IV and attenuation of titanium-particle-induced osteolysis. International Journal of Molecular Medicine, 36(5), 1335–1344. https://doi.org/10.3892/ijmm.2015.2330

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