Yang Ning, Cui Yueyi, Tan Jie, Fu Xin, Han Xiaoguang, Leng Huijie, Song Chunli
Department of Orthopedics, Peking University Third Hospital, Beijing, 100191, China.
J Bone Miner Metab. 2014 May;32(3):252-60. doi: 10.1007/s00774-013-0496-z. Epub 2013 Aug 10.
The aim of this study was to evaluate the effects and explore the mechanism of a local injection of a single dose of simvastatin as a strategy to strengthen target bone. Simvastatin was injected into the femurs (5 or 10 mg) or caudal vertebrae (1 or 2 mg) of ovariectomized rats, with an equal volume of vehicle injected as a control. Bone mineral density (BMD), bone microstructure and strength were evaluated at 1 and 5 months post-injection for the femurs and at 12 days post-injection for the vertebrae. Bone mass, adipocyte numbers and Runx2 expression were also examined using histology and immunohistochemistry. Compared with controls, simvastatin significantly increased BMD, bone volume fraction (BV/TV), improved bone microstructural parameters and bone strength in the femurs at both time points (all P < 0.01). Simvastatin-treated femurs contained fewer adipocytes and a higher Runx2 expression. For the caudal vertebrae, simvastatin significantly improved BV/TV, bone microstructures, and bone strength (all P < 0.01) as compared with controls. In conclusion, local injection of a single dose of simvastatin induces early onset and long-lasting bone augmentation in osteoporotic bone, significantly improving BMD, and bone microstructure and biomechanical strength. Simvastatin induces Runx2 expression, which may function to induce osteogenesis and inhibit adipogenesis as an underlying mechanism to augment bone mass.
本研究的目的是评估单次局部注射辛伐他汀作为强化目标骨的一种策略的效果,并探索其机制。将辛伐他汀注射到去卵巢大鼠的股骨(5或10毫克)或尾椎(1或2毫克)中,注射等体积的溶媒作为对照。在注射后1个月和5个月评估股骨的骨矿物质密度(BMD)、骨微结构和强度,在注射后12天评估尾椎的上述指标。还使用组织学和免疫组织化学检查骨量、脂肪细胞数量和Runx2表达。与对照组相比,辛伐他汀在两个时间点均显著增加了股骨的BMD、骨体积分数(BV/TV),改善了骨微结构参数和骨强度(所有P<0.01)。辛伐他汀处理的股骨中脂肪细胞较少,Runx2表达较高。对于尾椎,与对照组相比,辛伐他汀显著改善了BV/TV、骨微结构和骨强度(所有P<0.01)。总之,单次局部注射辛伐他汀可在骨质疏松性骨中诱导早期起效且持久的骨增强,显著改善BMD、骨微结构和生物力学强度。辛伐他汀诱导Runx2表达,这可能作为增加骨量的潜在机制发挥诱导成骨和抑制脂肪生成的作用。