[1,25 (OH)2D3局部应用对实验性大鼠牙齿运动的影响]。

M Kawakami
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引用次数: 0

摘要

本研究旨在探讨局部应用维生素D代谢物1,25二羟基胆钙化醇(1,25 (OH)2D3)对大鼠实验性牙齿运动的影响。1. 根据Waldo的方法,在体重200 g的Wistar雄性大鼠上第一磨牙和第二磨牙之间插入一根正畸弹性带。在右第一磨牙根分叉的腭粘膜下区局部注射20微升(10(-12)-10(-7)M) 1.25 (OH)2D3。左侧注射了车辆。在神经根间隔700 × 1050微米2的区域内计数破骨细胞的数量。在10(-10)m125 (OH)2D3时,破骨细胞数量呈剂量依赖性增加2倍。局部注射10(-10)m125 (OH)2D3后第3天,破骨细胞数量增加最多。2. 用螺旋弹簧将Wistar雄性大鼠上第一磨牙向颊部方向移动。局部给药10(-10)m125 (OH)2D3 20微升,每3天重复一次,直到第20天牺牲。1,25 (OH) 2d3处理大鼠的牙齿运动速度比对照大鼠加快约2倍。3.采用荧光标记法和定量组织学方法观察实验性动牙对骨形成的影响。因此,局部应用10(-10)m125 (OH)2D3有阻止正畸牙齿移动后牙槽骨矿物附着率下降的趋势。4. 1,25 (OH) 2d3处理的大鼠在最后一次注射后3小时从腹主动脉提取血清样本。钙、磷、碱性磷酸酶等参数值未见明显变化。上述结果提示,125 (OH)2D3局部应用于实验性大鼠牙齿运动,可导致破骨细胞数量增加,牙齿运动加速。然而,没有发现明显的副作用。1,25 (OH)2D3有望刺激紧张侧牙槽骨的矿物质附着率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Effects of local application of 1,25 (OH)2D3 on experimental tooth movement in rats].

The purpose of the present study was to explore the effect of local application with Vitamin D metabolite, 1,25 dihydroxycholecalciferol (1,25 (OH)2D3), on experimental tooth movement in rats. 1. According to Waldo's method, a piece of orthodontic elastic band was inserted between the upper first and second molars of Wistar male rats weighing 200 g. The amount of 20 microliters of 1,25 (OH)2D3(10(-12)-10(-7) M) was injected locally in the submucosal palatal area of the root bifurcation of the right first molar. The left side was injected with vehicle. The number of osteoclasts was counted in a 700 x 1050 micron 2 area of the inter-radicular septum. The number of osteoclasts was dose-dependently increased 2-fold at 10(-10) M 1,25 (OH)2D3 compared to that in the vehicle-injected side. The maximal increase of osteoclast number was observed 3 days after local injection of 10(-10) M 1,25 (OH)2D3 on experimental tooth movement. 2. The upper first molar of Wistar male rats was moved in a buccal direction by a helical spring. The amount of 20 microliters of the local administration of 10(-10) M 1,25 (OH)2D3 was repeated every 3 days until sacrifice at day 20. The tooth movement in the 1,25 (OH)2D3-treated rats was accelerated about 2-fold compared to that in the control rats. 3. The effect of bone formation in the rats receiving experimental tooth movement was examined by fluorescent labeling and quantitative histology. Thus, the local application of 10(-10) M 1,25 (OH)2D3 tended to prevent the decrease of the mineral apposition rate of the alveolar bone following orthodontic tooth movement. 4. Serum samples of these 1,25 (OH)2D3-treated rats was obtained from abdominal aorta 3 hours after the final injection. Serious effects were not found in the values for parameters such as calcium, phosphorus and alkaline phosphatase. These findings suggested that the local use of 1,25 (OH)2D3 on experimental tooth movement in the rats caused increase in osteoclasts number and accelerated tooth movement. However, no obvious side effects were noted. 1,25 (OH)2D3 was expected to stimulate mineral apposition rate of alveolar bone on the tension side.

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