Grove School of Engineering, City College and the Graduate Center of the City University of New York, New York, NY, USA.
Cells Tissues Organs. 2011;194(2-4):302-6. doi: 10.1159/000324236. Epub 2011 May 19.
Fourier transform infrared imaging spectroscopy (FTIRI)-assessed bone composition parameters (mineral content, collagen maturity, crystal size and perfection, and carbonate content) describe bone quality and correlate to bone fracture risk. The challenge with studying bone quality in patients treated with antiresorptive drugs such as bisphosphonates (e.g., alendronate) and selective estrogen receptor modulators (SERMs) (e.g. raloxifene) is being able to test bone mechanical performance and material properties pre- and posttreatment. The purpose of this study was to evaluate the FTIRI changes in a large animal model of osteoporosis (female sheep with dietary induced metabolic acidosis; MA). Previous studies have investigated the relationship between bone material properties and bone strength in humans and smaller animals and have shown that changes in compositional properties influence fracture risk. Here we characterize the MA model at 6 and 12 months, demonstrate the loss of bone and changes in compositional properties, and show that 6 months of treatment with both antiresorptives ameliorate the bone loss as assessed by bone mineral density and FTIRI. This preliminary data suggest that the MA sheep model allows investigation of whether drug treatments preserve bone properties that exist at the time of treatment or if they induce further beneficial changes.
傅里叶变换红外成像光谱(FTIRI)评估的骨成分参数(矿物质含量、胶原成熟度、晶体大小和完善度以及碳酸盐含量)描述了骨质量,并与骨折风险相关。在研究接受抗吸收药物(如双磷酸盐[例如,阿仑膦酸钠])和选择性雌激素受体调节剂(SERMs)[例如,雷洛昔芬]治疗的患者的骨质量时,面临的挑战是能够在治疗前后测试骨机械性能和材料特性。本研究的目的是评估骨质疏松症大动物模型(通过饮食诱导代谢性酸中毒的雌性绵羊;MA)中的 FTIRI 变化。先前的研究已经调查了人类和小型动物的骨材料特性与骨强度之间的关系,并表明组成特性的变化会影响骨折风险。在这里,我们在 6 个月和 12 个月时对 MA 模型进行了表征,证明了骨丢失和组成特性的变化,并表明用两种抗吸收剂治疗 6 个月可改善骨密度和 FTIRI 评估的骨丢失。这些初步数据表明,MA 绵羊模型可以研究药物治疗是否可以保留治疗时存在的骨特性,或者它们是否会引起进一步的有益变化。