Ross Ryan D, Sumner D Rick
Department of Cell & Molecular Medicine, Rush University Medical Center, Chicago, IL, 60612, USA.
Department of Orthopedic Surgery, Rush University Medical Center, Chicago, IL, USA.
Calcif Tissue Int. 2017 Aug;101(2):193-203. doi: 10.1007/s00223-017-0270-7. Epub 2017 Apr 3.
Matrix maturation within cortical bone is an important but oft-neglected component of bone remodeling because of the lack of a suitable small animal model. Intra-cortical remodeling can be induced in rodents by feeding virgin or lactating animals a low-calcium diet. The current study aimed to determine which of these two models is most suitable for studying intra-cortical matrix maturation. We compared intra-cortical remodeling in female rats fed a normal calcium diet (virgin/normal Ca), a low-calcium diet (virgin/low Ca), or a low-calcium diet during lactation (lactation/low Ca). The low-calcium diet was administered for 23 days (induction phase) followed by return to normal calcium for 30 days (recovery phase). At the end of induction, the virgin/normal Ca and virgin/low-Ca animals had no difference in cortical porosity, but the lactation/low-Ca animals had elevated cortical porosity at various diaphyseal sites in the femur and tibia. The distal femoral site had the greatest amount of induced porosity in the size range of rat secondary osteons. Neither global mineralization nor tissue age-specific mineral-to-matrix ratio in the bone formed during recovery were affected in the lactation/low-Ca rats. Serum calcium levels did not differ from controls, but phosphate levels were slightly elevated, consistent with the rapid recovery of lost bone mass. We conclude that the lactation/low-Ca model represents a means to increase intra-cortical remodeling in adult rats with no apparent detrimental effect on matrix maturation. This model will provide researchers with a new tool to study matrix maturation throughout the cortex.
由于缺乏合适的小动物模型,皮质骨内的基质成熟是骨重塑过程中一个重要但常被忽视的组成部分。通过给未生育或哺乳期的动物喂食低钙饮食,可以诱导啮齿动物进行皮质内重塑。本研究旨在确定这两种模型中哪一种最适合用于研究皮质内基质成熟。我们比较了喂食正常钙饮食(未生育/正常钙)、低钙饮食(未生育/低钙)或哺乳期低钙饮食(哺乳期/低钙)的雌性大鼠的皮质内重塑情况。低钙饮食持续23天(诱导期),随后恢复正常钙饮食30天(恢复期)。在诱导期结束时,未生育/正常钙组和未生育/低钙组动物的皮质孔隙率没有差异,但哺乳期/低钙组动物在股骨和胫骨的不同骨干部位皮质孔隙率升高。股骨远端部位在大鼠次级骨单位大小范围内诱导出的孔隙率最高。恢复期形成的骨组织中的整体矿化以及特定组织年龄的矿化与基质比率在哺乳期/低钙大鼠中均未受影响。血清钙水平与对照组无差异,但磷酸盐水平略有升高,这与丢失骨量的快速恢复一致。我们得出结论,哺乳期/低钙模型是一种增加成年大鼠皮质内重塑的方法,且对基质成熟没有明显的有害影响。该模型将为研究人员提供一个研究整个皮质基质成熟的新工具。