Publications by authors named "Changheng Song"

Article Synopsis
  • MZGW (Modified Zuo Gui Wan) combines traditional herbal treatment and red yeast rice, showing promise in treating osteoporosis (OP) through its effects on osteoclasts.
  • Research utilized both in vivo (OVX rat model) and in vitro (RANKL-induced osteoclasts) experiments to understand MZGW's mechanisms, particularly focusing on the SCFA-GPR41-p38MAPK signaling pathway.
  • Results indicated that the high-dose MZGW improved bone microstructure and inhibited osteoclast activity by changing gut flora metabolism and effectively regulating specific signaling pathways.
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Article Synopsis
  • Abnormal macrophage polarization contributes to various inflammatory diseases, leading researchers to explore methods to change macrophage behavior for better treatment options.
  • Icariin (ICA) shows promise in regulating macrophage polarization, but its use is limited due to issues like poor water solubility and low effectiveness in the body.
  • The new delivery system, ADSC-derived exosomes (ADSCs-EXO) combined with ICA, demonstrates high drug loading and significantly enhances anti-inflammatory effects by effectively shifting harmful M1 macrophages to a healthier M2 type through specific signaling pathway modulation.
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Diosgenin (DIO) is an aglycone of steroid saponins acquired from plants, including Dioscorea alata, Smilax China, and Trigonella foenum graecum, acting as an anti-osteoporosis, anti-diabetic, anti-hyperlipidemic, anti-inflammatory. Recent studies have demonstrated that DIO reduces bone loss. This study aimed to investigate the effects of DIO on the gut microbiota (GM) of ovariectomized (OVX) osteoporotic rats.

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Objective: This study is aimed at predicting and contrasting the mechanisms of artemisinin (ARS), dihydroartemisinin (DHA), artesunate (ART), artemether (ARM), and arteether (ARE) in the treatment of osteoporosis (OP) using network pharmacology and molecular docking.

Methods: The targets of ARS, DHA, ART, ARM, and ARE were obtained from the SwissTargetPrediction. The targets related to OP were obtained from the TTD, DrugBank, Genecards, and DisGeNet databases.

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Osteoclasts are the only multinucleated cells in vivo responsible for bone resorption and are vital for regulating bone remodeling and maintaining bone mass. The RAW264.7 cell line is widely used to study osteoclastic differentiation and biological molecular mechanism.

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Ethnopharmacological Relevance: Er-Xian decoction (EXD) is a traditional Chinese medicine (TCM) formula used to treat osteoporosis (OP). However, the anti-OP mechanism of EXD has not yet been fully elucidated.

Aim Of The Study: The study aimed to verify the anti-OP effect of EXD and to explore its underlying mechanism.

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Osteoclasts (OCs) are multinucleated cells that play a major role in osteolytic diseases such as osteoporosis. Monascin (Ms) is one of the active substances in the traditional Chinese medicine red yeast rice. Studies have found that red yeast rice can maintain bone health.

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Rhizoma Dioscoreae extract (RDE) exhibits a protective effect on alveolar bone loss in ovariectomized (OVX) rats. The aim of this study was to predict the pathways or targets that are regulated by RDE, by re‑assessing our previously reported data and conducting a protein‑protein interaction (PPI) network analysis. In total, 383 differentially expressed genes (≥3‑fold) between alveolar bone samples from the RDE and OVX group rats were identified, and a PPI network was constructed based on these genes.

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The aim of this study was to evaluate the osteoprotective effect of aqueous Rhizoma Dioscoreae extract (RDE) on the alveolar bone of rats with ovariectomy-induced bone loss. Female Wistar rats underwent either ovariectomy or sham operation (SHAM). The ovariectomized (OVX) rats were treated with vehicle (OVX), estradiol valerate (EV), or RDE.

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The aim of this study was to evaluate effect of diosgenin (DG) on rats that had osteoporosis-like features induced by ovariectomy (OVX). Seventy-two six-month-old female Wistar rats were subjected to either ovariectomy (n = 60) or Sham operation (SHAM group, n = 12). Beginning at one week post-ovariectomy, the OVX rats were treated with vehicle (OVX group, n = 12), estradiol valerate (EV group, n = 12), or DG at three doses (DG-L, -M, -H group, n = 12, respectively).

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