Li, Hongbo, Liao, Xingen, Lan, Min, He, Jianying, Gao, Jingping, Fan, Zhiqiang, Huang, Jiayu, Wu, Xin, Chen, Jiaxin, and Sun, Guicai
Arctigenin (Ar) is a promising therapeutic candidate for postmenopausal osteoporosis (PMOP). This study explores its mechanism by examining its effects on adipogenesis and osteogenesis in ovariectomized (OVX) rats. In vitro, Ar effectively suppressed the adipogenic differentiation of bone marrow mesenchymal stem cells (BMSCs) from OVX rats, reducing lipid droplet formation and downregulating proteins associated with lipid synthesis. In vivo, Ar treatment significantly reduced bone loss, inhibited adipocyte development, improved lipid metabolism, and promoted bone formation in OVX rats. Mechanistically, Ar inhibited the phosphorylation of Mitogen‐Activated Protein Kinase 1 (MEK1), downregulated Peroxisome Proliferator‐Activated Receptor gamma (PPARγ), promoted the accumulation of β‐catenin in the nucleus, and prevented the direct binding of PPARγ to β‐catenin in BMSCs. This regulation of the PPARγ/Wnt signaling axis underlies its dual role in inhibiting adipogenesis and promoting osteogenesis. Notably, co‐treatment with rosiglitazone (RGZ) reversed the effects of Ar on adipogenesis and osteogenesis without affecting MEK1 inhibition. These findings offer valuable insights into arctigenin's potential as a therapeutic strategy for PMOP by modulating MEK1 signaling and regulating the PPARγ/Wnt axis. [ABSTRACT FROM AUTHOR]