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Antiosteoporotic Effects of Huangqi Sanxian Decoction in Cultured Rat Osteoblasts by Proteomic Characterization of the Target and Mechanism. | LitMetric

Antiosteoporotic Effects of Huangqi Sanxian Decoction in Cultured Rat Osteoblasts by Proteomic Characterization of the Target and Mechanism.

Evid Based Complement Alternat Med

Department of Pharmacy, Guangdong Medical College, No. 1, Xincheng Dadao, Songshan Lake Science and Technology Industry Park, Dongguan 523808, China.

Published: November 2015

AI Article Synopsis

  • * A study using seropharmacology and proteomic methods revealed that HQSXD significantly improves the proliferation, differentiation, and mineralization of osteoblasts (bone-forming cells).
  • * The research identified changes in specific proteins linked to cell growth and signaling, suggesting how HQSXD may exert its antiosteoporotic effects in osteoblasts.

Article Abstract

Huangqi Sanxian decoction (HQSXD) is routinely used for the treatment of osteoporosis in the Chinese traditional healthcare system. However, the targets and mechanism underlying the effect of HQSXD on osteoporosis have not been documented. In the present study, seropharmacology and proteomic approaches (two-dimensional gel electrophoresis combined with mass spectrometry) were used to investigate the effects and possible target proteins of HQSXD on osteoblast. We found that HQSXD-treated rat serum significantly enhanced osteoblast proliferation, differentiation, and mineralization. In HQSXD-S-treated osteoblasts, there were increases in the expression of N-formyl peptide receptor 2 and heparan sulfate (glucosamine) 3-O-sulfotransferase 3A1 and reduction in the expression of alpha-spectrin, prohibitin, and transcription elongation factor B (SIII), polypeptide 1. The identified proteins are associated with cell proliferation, differentiation, signal transcription, and cell growth. These findings might provide valuable insights into the mechanism of antiosteoporotic effect affected by HQSXD treatment in osteoblasts.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4628673PMC
http://dx.doi.org/10.1155/2015/514063DOI Listing

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