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.
引用
收藏
页码:6 / 13
页数:8
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