γ-Tocotrienol protects against ovariectomy-induced bone loss via mevalonate pathway as HMG-CoA reductase inhibitor

被引:44
作者
Deng, Lili [1 ]
Ding, Yuedi [1 ]
Peng, Ying [1 ]
Wu, Yu [1 ]
Fan, Jun [1 ]
Li, Wenxin [1 ]
Yang, Runlin [1 ]
Yang, Meiling [2 ]
Fu, Qiang [1 ]
机构
[1] Jiangsu Inst Nucl Med, Key Lab Nucl Med, Minist Hlth, Jiangsu Key Lab Mol Nucl Med, Wuxi 214063, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Affiliated Hosp 1, Nanjing, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Bone loss; HMG-CoA reductase inhibitor; Mevalonate pathway; gamma-Tocotrienol; KAPPA-B LIGAND; VITAMIN-E; OSTEOCLAST FORMATION; MALE RATS; IN-VITRO; CHOLESTEROL-BIOSYNTHESIS; ANTIOXIDANT ACTIVITIES; RECEPTOR ACTIVATOR; MINERAL DENSITY; GENE-EXPRESSION;
D O I
10.1016/j.bone.2014.07.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
gamma-Tocotrienol (GT3), an analogue of vitamin E, has gained increasing scientific interest recently as it provides significant health benefits. GT3 exerts its biological effects not only by virtue of antioxidant properties but also by inhibiting hydroxy-methyl-glutaryl-coenzyme A (HMG-CoA) reductase. Studies have reported that the mevalonate pathway is relevant for bone metabolism and HMG-CoA reductase inhibitors can increase bone mass and are useful in osteoporosis therapy. However, whether it is involved in the bone anabolic activity of GT3 is not clear. This study was conducted to investigate the ability of GT3 to protect against ovariectomy-induced bone loss, as well as the correlation between the protections and mevalonate pathway. Results showed that mice supplemented with 100 mg/kg emulsified GT3 via subcutaneous injection once per month for three months were significantly protected from ovariectomy-induced bone loss as evaluated by various bone structural parameters, bone metabolic gene expression levels and serum levels of biochemical markers for bone resorption and bone formation. Importantly, the effect of GT3 on preventing against ovariectomy-induced bone loss could be reversed by daily supplementation with mevalonate, indicating that GT3 may via an HMG-CoA reductase-dependent mechanism to protect against ovariectomy-induced bone loss. Our results suggest that GT3 is suitable as dietary supplement and has potential as an alternative drug to treat or prevent osteoporosis. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:200 / 207
页数:8
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