Antrodia cinnamomea prevents ovariectomized-promoted bone loss by inhibiting osteoclast formation.
Chang Po-ChunHui-Kan SuShan-Chi LiuLe Huynh Hoai ThuongYang-Chang WuHsien-Te ChenTung-Ying WuChih-Hsin TangPublished in: Environmental toxicology (2024)
Osteoporosis is a common bone disease in aging populations, particularly in postmenopausal women. Anti-resorptive and anabolic drugs have been applied to prevent and cure osteoporosis and are linked with a variety of adverse effects. Antrodia cinnamomea extracts (ACE) are highly renowned for their anticancer, antioxidative, and anti-inflammatory properties. However, whether ACE-enriched anti-osteoporosis functions are largely unknown. In a preclinical animal model, we found that ovariectomy significantly decreased bone volume in the ovariectomized (OVX) rats. Administration of ACE antagonized OVX-induced bone loss. In addition, ACE reversed OVX-reduced biomechanical properties. The serum osteoclast marker also showed improvement in the ACE-treated group. In the cellular model, it was indicated that ACE inhibits RANKL-induced osteoclast formation. Taken together, ACE seems to be a hopeful candidate for the development of novel anti-osteoporosis treatment.
Keyphrases
- bone loss
- postmenopausal women
- bone mineral density
- angiotensin converting enzyme
- angiotensin ii
- anti inflammatory
- high glucose
- drug induced
- body composition
- diabetic rats
- signaling pathway
- stem cells
- immune response
- mesenchymal stem cells
- inflammatory response
- endothelial cells
- cell therapy
- mouse model
- stress induced
- replacement therapy