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Naringin Alleviates H(2)O(2)-Inhibited Osteogenic Differentiation of Human Adipose-Derived Stromal Cells via Wnt/β-Catenin Signaling

Osteoporosis is an age-related systemic bone disease that places a heavy burden on patients and society. In this study, we aimed to investigate the effects of naringin (NAR) on the osteogenic differentiation of human adipose-derived stromal cells (ADSCs). The results demonstrated that NAR pretreatme...

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Detalles Bibliográficos
Autores principales: Yang, Xufang, Dong, Jianjiang, Hao, Yankun, Qi, Yucheng, Liang, Jun, Yan, Lei, Wang, Wenting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9076301/
https://www.ncbi.nlm.nih.gov/pubmed/35529937
http://dx.doi.org/10.1155/2022/3126094
Descripción
Sumario:Osteoporosis is an age-related systemic bone disease that places a heavy burden on patients and society. In this study, we aimed to investigate the effects of naringin (NAR) on the osteogenic differentiation of human adipose-derived stromal cells (ADSCs). The results demonstrated that NAR pretreatment effectively abated H(2)O(2)-induced cell death and ROS accumulation in ADSCs undergoing osteogenic differentiation (ADSCs-OD). In addition, we also observed that the impaired extracellular matrix mineralization and ALP activity in H(2)O(2)-stimulated ADSCs-OD were notably rescued by NAR pretreatment. Moreover, the effects of H(2)O(2) exposure on Wnt/β-catenin signaling in ADSCs-OD were largely reversed by NAR pretreatment. Collectively, our findings indicated that NAR could protect ADSCs-OD against H(2)O(2)-inhibited osteogenic differentiation.