破骨细胞
组织蛋白酶K
去卵巢大鼠
兰克尔
骨质疏松症
骨吸收
化学
MAPK/ERK通路
内分泌学
内科学
癌症研究
骨髓
蛋白激酶B
没食子酸
细胞生物学
医学
信号转导
生物化学
生物
雌激素
受体
激活剂(遗传学)
抗氧化剂
作者
Peng Zhang,Jiekai Ye,Jiale Dai,Ying Wang,Genjun Chen,Jinping Hu,Qimiao Hu,Jun Fei
标识
DOI:10.3389/fendo.2022.963237
摘要
Osteoporosis is a common metabolic bone disease with a rapidly increasing prevalence, characterized by massive bone loss because of excessive osteoclast formation. Gallic acid (GA), a phenolic acid isolated from Cornus officinalis , has anti-inflammatory and anti-oxidant effects, but its effect on osteoclast formation has not been confirmed. In our study, we demonstrated that GA significantly inhibited RANKL‐induced osteoclast formation and function of osteoclast in bone marrow monocytes (BMMs) and RAW264.7 cells in a dose-dependent manner without cytotoxicity. For molecular mechanisms, GA repressed osteoclastogenesis by blocking Akt, ERK, and JNK pathways, and suppressed osteoclastogenesis-related marker expression, including nuclear factor of the activated T-cell cytoplasmic 1 (NFATc1), c‐Fos, and cathepsin K (CTSK). In addition, we further assessed the effect of GA in an ovariectomized mouse model, which indicated that GA has a notable effect on preventing bone loss. In conclusion, GA exerts notable effects in inhibiting osteoclastogenesis and preventing ovariectomy-induced bone loss, suggesting that GA is a potential agent in osteoporosis treatment.
科研通智能强力驱动
Strongly Powered by AbleSci AI