Monotropein isolated from the roots of Morinda officinalis increases osteoblastic bone formation and prevents bone loss in ovariectomized mice

被引:50
作者
Zhang, Zhiguo [1 ]
Zhang, Qiaoyan [1 ]
Yang, Hua [3 ]
Liu, Wei [2 ]
Zhang, Naidan [1 ]
Qin, Luping [1 ]
Xin, Hailiang [1 ]
机构
[1] Second Mil Med Univ, Sch Pharm, Dept Pharmacognosy, Shanghai, Peoples R China
[2] 88th Hosp PIA, Dept Pharm, Tai An, Shandong, Peoples R China
[3] Taishan Med Coll, Dept Immunol, Tai An, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Morinda officinalis; Monotropein; Osteoporosis; Ovariectomy; Osteoblast; ANTIOSTEOPOROTIC ACTIVITY; IN-VITRO; OSTEOPOROSIS; INTERLEUKIN-6; MACROPHAGES; RECEPTOR; CELLS; RATS;
D O I
10.1016/j.fitote.2016.03.013
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Monotropein is a natural iridoid glycoside enriched in Morinda officinalis and has been used for medicinal purposes in China. In the present study, we systematically examined its effects on ovariectomy (OVX)-induced osteoporosis in mice and osteoblastic MC3T3-E1 cells for the first time. Eight-week-old female C57/BL6 mice were used to evaluate the osteoprotective effect of monotropein. Results showed that administration of monotropein (40 or 80 mg/kg/day) for four weeks exerted good bone protective effects as evidenced by the increase of bone mineral content (BMC), bone mineral density (BMD), bone volume fraction (8W) and improvement of bone microstructure. Monotropein also enhanced the parameters of biomechanital properties, including maximum load, maximum stress and elastic modulus of femur in OVX nice. In addition, monotropein treatment decreased the serum levels of interleukin 1 (IL-1), interleukin 6 (IL-6) and soluble receptor activator of NF-kappa B ligand (sRANKL) in OVX mice. In this study, we also assessed the effects of monotropein on the proliferation and differentiation of osteoblastic MC3T3-E1 cells in vitro. After incubation for 48 h, the cell proliferation was increased at the concentration of 10 mu M, 25 mu M, 50 mu M and 100 mu M. ALP activities were significantly increased after treatment with monotropein for 72 h. Quantitative analyses with alizarin red staining showed significantly increased mineralization of MC3T3-E1 cells after treatment with monotropein for 28 days. Based on these results, monotropein may serve as a new candidate or a leading compound for antiosteoporosis. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:166 / 172
页数:7
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