Melatonin prevents bone destruction in mice with retinoic acid–induced osteoporosis

Molecular Medicine

Yuanxin Zhu¹  Anjing Liang¹  Yan Peng¹  Bo Gao¹  Dongsheng Huang¹  Xudong Wang¹  Jincheng Qiu¹  Tongzhou Liang¹  Xianjian Qiu¹  Hang Zhou²  Chengjie Lian²  Xiaoming Yang²  Zhiheng Liao²  Peiqiang Su²  Caixia Xu³  Yongyong Li³ 

[1] Department of Orthopedics, Sun Yat-sen Memorial Hospital of Sun Yat-sen University, #107 West Yan Jiang Road, 510120, Guangzhou, Guangdong, China;Department of Orthopedics, the First Affiliated Hospital of Sun Yat-sen University, #58 Zhongshan Road II, 510080, Guangzhou, Guangdong, China;Research Centre for Translational Medicine, the First Affiliated Hospital of Sun Yat-sen University, 510080, Guangzhou, Guangdong, China;

关键词: Osteoporosis;    Melatonin;    Bone metabolism;    Bone remodeling;    Oxidant stress;   

DOI  :  10.1186/s10020-019-0107-0

来源: Springer

【 摘 要 】

BackgroundThe protective effect of melatonin against bone metabolism imbalance in osteoporosis (OP) induced by drugs such as retinoic acid (RA) is unclear. The aim of this study was to explore the role of melatonin in bone destruction based on a mouse model.MethodsRA-induced OP model mice were established. To assess the effect of melatonin on these mice, micro-CT was used to characterize the trabecular structure of normal mice and those treated with RA (model), RA + low-dose melatonin (Mlt-L), RA + high-dose melatonin (Mlt-H), and RA + alendronate sodium (positive control). The shape of the trabecular bone, the length and diameter of the femoral head and the height and diameter of vertebra(L1) of each group were also measured and the number of osteoclasts was determined by Tartrate-resistant acid phosphatase (TRACP) staining. Meanwhile, the expression of alkaline phosphatase (ALP) was evaluated by immunohistochemistry assays. The differences between groups in terms of liver and kidney oxidation–related indexes and serum and urinary indicators related to bone metabolism were also analyzed. Furthermore, qRT-PCR and western blotting were used to evaluate the effect of melatonin on osteogenic and osteoclastic differentiation in MC3T3-E1 and RAW264.7 cells, respectively.ResultsRA induction led to a decrease in the amount and density of trabecular bone, a decrease in the length and diameter of the femur and height, diameter of the vertebra (L1), a decrease in bone mass and density and the expression of ALP, and an increase in the number of osteoclasts. Melatonin treatment alleviated these effects induced by RA, increasing the amount of trabecular bone in OP mice, improving the microstructure of the femur and vertebra(L1) and increasing bone mass bone density and the expression of ALP, as well as decreasing the number of osteoclasts. Additionally, blood and urinary bone metabolism-related indicators showed that melatonin promoted bone formation and inhibited bone resorption. Determination of oxidant and antioxidant biomarkers in the livers and kidneys of the mice revealed that melatonin promoted the antioxidant level and suppressed the level of oxidant molecules in these organs. In vitro, RA promoted osteoclasts and inhibit osteogenesis by increasing oxidative stress levels in the RAW264.7 and MC3T3-E1 cells, but melatonin reversed this effect. Melatonin may, therefore, play a role in the ERK/SMAD and NF-κB pathways.ConclusionsMelatonin can alleviate bone loss in RA-induced OP model mice, repair the trabecular microstructure, and promote bone formation. These effects may be related to reducing oxidation levels in vivo and vitro through the ERK/SMAD and NF-κB pathways.

【 授权许可】

CC BY