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Icariin inhibits RANKL-induced osteoclastogenesis in RAW264.7 cells via inhibition of reactive oxygen species production by reducing the expression of NOX1 and NOX4
被引:13
作者:
Ji, Ruifeng
[1
]
Wu, Dou
[1
]
Liu, Qiang
[1
]
机构:
[1] Third Hosp Shanxi Med Univ, Shanxi Acad Med Sci, Shanxi Bethune Hosp, Dept Orthoped,Tongji Shanxi Hosp,Hosp 3, 99 Longcheng St, Taiyuan 030032, Shanxi, Peoples R China
关键词:
Icariin;
Reactive oxygen species;
Osteoclastogenesis;
NADPH OXIDASES;
BONE LOSS;
DIFFERENTIATION;
ESTROGEN;
LIGAND;
D O I:
10.1016/j.bbrc.2022.02.023
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Icariin (ICA), isolated from Herba Epimedii, is a natural flavonoid glycoside that possesses antioxidant properties and inhibits osteoclastogenesis. However, the mechanism underlying osteoclastogenesis in-hibition by ICA remains unclear. Here, we investigated the effects of ICA on receptor activator of nuclear factor kappa-B ligand (RANKL)-induced osteoclastogenesis in RAW264.7 cells. ICA inhibited the expression of osteoclastogenesis-related genes in RAW264.7 cells induced by RANKL. ICA could inhibit osteoclastogenesis without inhibiting the viability of RAW264.7 cells. In addition, ICA inhibited reactive oxygen species production in RANKL-induced RAW264.7 cells. ICA reduced the expression of nuclear factor in activated T cells, cytoplasmic 1, and tartrate-resistant acid phosphatase, which are osteoclast-related molecules. Moreover, ICA decreased the expression of nicotinamide adenine dinucleotide phosphate oxidase (NOX), specifically NOX1 and NOX4, in RANKL-induced RAW264.7 cells. Our findings suggest that ICA can be used as a potential therapeutic agent for osteolytic diseases such as osteoporosis. (C) 2022 Elsevier Inc. All rights reserved.
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页码:6 / 13
页数:8
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