自噬
骨质疏松症
骨重建
骨吸收
激素
医学
骨量
内分泌学
吸收
内生
内科学
生物
细胞生物学
细胞凋亡
生物化学
作者
Tiantian Wang,Hongchen He,Sha-Xin Liu,Cheng-sen Jia,Fan Ziyan,Can Zhong,Jiadan Yu,Honghong Liu,Chengqi He
出处
期刊:Current Drug Targets
[Bentham Science]
日期:2019-02-28
卷期号:20 (3): 354-365
被引量:15
标识
DOI:10.2174/1389450119666180626120852
摘要
Autophagy is a process the primary role of which is to clear up damaged cellular components such as long-lived proteins and organelles, thus participating in the conservation of different cells. Osteoporosis associated with aging is characterized by consistent changes in bone metabolism with suppression of bone formation as well as increased bone resorption. In advanced age, not only bone mass but also bone strength decrease in both sexes, resulting in an increased incidence of fractures. Clinical and animal experiments reveal that age-related bone loss is associated with many factors such as accumulation of autophagy, increased levels of reactive oxygen species, sex hormone deficiency, and high levels of endogenous glucocorticoids. Available basic and clinical studies indicate that age-associated factors can regulate autophagy. Those factors play important roles in bone remodeling and contribute to decreased bone mass and bone strength with aging. In this review, we summarize the mechanisms involved in bone metabolism related to aging and autophagy, supplying a theory for therapeutic targets to rescue bone mass and bone strength in older people.
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