4.7 Article

Pteryxin suppresses osteoclastogenesis and prevents bone loss via inhibiting the MAPK/Ca2+signaling pathways mediated by ROS

Journal

BIOMEDICINE & PHARMACOTHERAPY
Volume 165, Issue -, Pages -

Publisher

ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.biopha.2023.114898

Keywords

Pteryxin; Osteoclast; ROS; MAPK; Ca2+

Ask authors/readers for more resources

Osteoporosis is a severe global public health problem that causes damage to bone mass, strength, and microstructure, increasing the risk of fragility fractures. The use of current prescription medications for osteoporosis treatment has adverse effects, so finding natural alternatives is important. Pteryxin (PTX), a natural coumarin, has been found to have antioxidant, anti-inflammatory, and anti-obesity properties. Studies have shown that PTX can reduce osteoclast formation and bone resorption, and partially reverse bone loss in an osteoporosis model. Its mechanism of action involves blocking specific signaling pathways and reducing reactive oxygen species (ROS) levels in osteoclasts. Overall, PTX may offer a new or alternative treatment option for osteoporosis.
Osteoporosis, as a severe public health problem worldwide, causes systemic damage to bone mass, strength, and microstructure with an increased propensity for fragility fractures. Given the inherent adverse effects associated with long-term use of current prescription medications for osteoporosis treatment, identifying natural alternatives to existing treatment methods is imperative. Pteryxin (PTX), a natural coumarin, is isolated from the Peucedanum species belonging to the family Apiaceae. PTX has been reported to have antioxidant, antiinflammatory and anti-obesity properties. However, its effect on osteoporosis has not been clarified. Our study confirmed that PTX could attenuate the formation of osteoclasts and bone resorption on a dose-dependent basis in vitro. Consistently, in vivo ovariectomy (OVX)-induced osteoporosis models simulating the physiological characteristics of postmenopausal women showed that PTX could partially reverse the bone loss caused by OVX. Further study of its mechanism revealed that PTX might block the MAPK and Ca2+-calcineurin-NFATc1 signaling pathways by decreasing the reactive oxygen species (ROS) level in osteoclasts to dampen the expression of critical transcriptional NFATc1 and downstream osteoclast-specific genes. Overall, PTX may present a new or alternative treatment option for osteoporosis.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available