Tran Van P T, Vignery A, Baron R
Anat Rec. 1982 Apr;202(4):445-51. doi: 10.1002/ar.1092020403.
The kinetics of the bone remodeling sequence in the rat has been studied using a system in which well-synchronized remodeling units were induced along the periosteum of rat mandibles. Remodeling of the periosteal surface of the mandibles was induced according to Tran Van (1979) by extraction of the opposing row of teeth; namely, the right maxillary molars were extracted under light ether anesthesia, therefore allowing the right mandibular molars to egress; this, in turn, induced a wave of remodeling activity on the buccal side of the periosteal surface of the alveolar bone. The quantification of the different cellular activities involved in bone remodeling has been performed up to 16 days after induction. This allowed us to demonstrate the sequential activity of the different cell types involved in bone remodeling, to study the cellular kinetics of this sequence of events, and to directly measure the duration of each phase of the bone remodeling sequence. A single wave of osteoclasts appeared 3 days after induction, reached a peak of 4-5 days, and then decreased sharply. This was followed by a single wave of mononuclear cells (Baron et al., 1980) within remodeling sites during the reversal phase; they appeared 4 days after induction, reached a peak by day 7, and then decreased sharply. This reversal activity was then followed by osteoblasts forming new bone on top of a reversal cement line in the remodeling sites, starting 6 days after induction and increasing until the end of the experiment. In addition, the synchronization of the system used in this study allowed direct measurement of the duration of the successive steps of the remodeling sequence. The directly measured values have then been compared to previous data calculated from other systems.
利用一种系统研究了大鼠骨重塑序列的动力学,在该系统中,沿大鼠下颌骨骨膜诱导出同步良好的重塑单元。根据Tran Van(1979年)的方法,通过拔除对侧一排牙齿来诱导下颌骨骨膜表面的重塑;即在轻度乙醚麻醉下拔除右上颌磨牙,从而使右下颌磨牙萌出;这反过来又在牙槽骨骨膜表面的颊侧诱导出一波重塑活动。在诱导后长达16天的时间里,对参与骨重塑的不同细胞活动进行了量化。这使我们能够证明参与骨重塑的不同细胞类型的顺序活动,研究这一系列事件的细胞动力学,并直接测量骨重塑序列各阶段的持续时间。诱导后3天出现一波破骨细胞,在4-5天达到峰值,然后急剧下降。随后在逆转期,重塑部位出现一波单核细胞(Baron等人,1980年);它们在诱导后4天出现,在第7天达到峰值,然后急剧下降。这种逆转活动之后是成骨细胞在重塑部位的逆转黏合线顶部形成新骨,从诱导后6天开始并持续增加直至实验结束。此外,本研究中使用的系统的同步性允许直接测量重塑序列连续步骤的持续时间。然后将直接测量的值与从其他系统计算出的先前数据进行比较。