Lee Don-Gil, Park Sang-Yong, Chung Won-Seok, Park Jae-Hee, Shin Heon-Sub, Hwang Eunson, Kim In-Ho, Yi Tae-Hoo
Department of Oriental Medicinal Materials & Processing, College of Life Science, Kyung Hee University, Gyeonggi-do, Republic of Korea.
Mol Nutr Food Res. 2014 Jun;58(6):1249-57. doi: 10.1002/mnfr.201300319. Epub 2014 Mar 7.
The aim of this study was to investigate the bone regenerative effects of fucosterol in estrogen-deficient ovariectomized (OVX) rats.
Bone regeneration was assessed in fucosterol-treated MG63 cells in vitro via assays for osteoblast proliferation, alkaline phosphatase, and osteoclast differentiation. Osteoblast proliferation rates, alkaline phosphatase activity, and mineralization were increased in the fucosterol-treated group. Moreover, differentiation of osteoclasts was decreased in the fucosterol-treated group. In the in vivo assay, female rats were OVX. Twelve weeks after ovariectomy, rats were divided into seven groups, each oral administrate everyday for 7 weeks. The bone mineral density of femoral bones was higher in fucosterol groups than in OVX control, and body weight was lower in fucosterol groups. Among bone-quality parameters, bone volume/total volume increased and trabecular separation decreased in fucosterol groups relative to the OVX control. Bone formation and resorption were evaluated using the serum biomarkers osteocalcin and CTx. Fucosterol tripled the level of serum osteocalcin relative to the OVX group and reduced the serum level of CTx.
These results suggest that fucosterol has the dual potentials to activate osteoblasts to stimulate bone formation and suppress differentiation of osteoclasts so as to reduce bone resorption.
本研究旨在调查岩藻甾醇对雌激素缺乏的去卵巢(OVX)大鼠的骨再生作用。
通过成骨细胞增殖、碱性磷酸酶和破骨细胞分化检测,在体外评估岩藻甾醇处理的MG63细胞中的骨再生情况。岩藻甾醇处理组的成骨细胞增殖率、碱性磷酸酶活性和矿化作用均有所增加。此外,岩藻甾醇处理组的破骨细胞分化减少。在体内试验中,对雌性大鼠进行去卵巢手术。卵巢切除术后12周,将大鼠分为七组,每组每天口服给药7周。岩藻甾醇组股骨的骨矿物质密度高于OVX对照组,且岩藻甾醇组的体重较低。在骨质量参数方面,相对于OVX对照组,岩藻甾醇组的骨体积/总体积增加,小梁间距减小。使用血清生物标志物骨钙素和CTx评估骨形成和骨吸收情况。相对于OVX组,岩藻甾醇使血清骨钙素水平增加了两倍,并降低了血清CTx水平。
这些结果表明,岩藻甾醇具有双重作用,既能激活成骨细胞以刺激骨形成,又能抑制破骨细胞分化从而减少骨吸收。