Talic Nabeel F, Evans Carla, Zaki A Moneim
Orthodontic Division, Department of Preventive Dentistry, King Saud University, Riyadh, Saudi Arabia.
Am J Orthod Dentofacial Orthop. 2006 Feb;129(2):252-60. doi: 10.1016/j.ajodo.2004.11.030.
Induced dental root resorption is a common side effect of orthodontic treatment. It is an unpredictable phenomenon, and its etiology is unknown. Odontoclasts responsible for the resorption of the dental tissues--ie, cementum and dentin--share many cytochemical and morphological characteristics with osteoclasts, which are responsible for bone resorption. The aim of this study was to explore cellular mechanisms that decrease induced root resorption in orthodontically treated teeth.
The effects of targeting the alphavbeta3 integrin receptor, expressed by odontoclasts, on induced root resorption surface areas and the number of root resorption lacunae were investigated by using an RGD-containing peptide, echistatin. The effect of echistatin on the number of clast cells in the periodontium was also examined. Tooth movement was achieved in 14 Sprague-Dawley rats by placing elastic bands between the right maxillary first and second molars for 24 hours. The animals were equally divided into 2 groups; the experimental animals received echistatin intravenously for 8 hours (0.8 microg/kg/min), and the controls received sterile water. The specimens obtained were processed for light microscopy. The surface area and the number of root resorption lacunae were measured histomorphometrically by using digital photomicrographs. Echistatin labeled with a fluorescent marker was used to confirm its presence in clast cells with fluorescent microscopy. Cytochemically, tartrate-resistant acid phosphatase was used to quantify mature and committed clast cells. Echistatin was localized in targeted cells in the periodontium.
Echistatin significantly decreased root resorption surface areas (P < .01) and reduced the number of root resorption lacunae (P < .01). There was no statistically significant difference in clast cell numbers.
Targeting alphavbeta3 integrin receptor expressed by odontoclasts can be effective in reducing root resorption during tooth movement. Further studies are needed to elucidate the mechanism of this inhibition.
诱导性牙根吸收是正畸治疗常见的副作用。这是一种不可预测的现象,其病因尚不清楚。负责牙组织(即牙骨质和牙本质)吸收的破牙细胞与负责骨吸收的破骨细胞具有许多细胞化学和形态学特征。本研究的目的是探索减少正畸治疗牙齿诱导性牙根吸收的细胞机制。
使用含RGD的肽echistatin研究靶向破牙细胞表达的αvβ3整合素受体对诱导性牙根吸收表面积和牙根吸收陷窝数量的影响。还检测了echistatin对牙周组织中破骨细胞数量的影响。通过在14只Sprague-Dawley大鼠的右上颌第一和第二磨牙之间放置弹性带24小时来实现牙齿移动。将动物平均分为2组;实验动物静脉注射echistatin 8小时(0.8微克/千克/分钟),对照组注射无菌水。对获得的标本进行光学显微镜处理。使用数码显微照片通过组织形态计量学测量牙根吸收陷窝的表面积和数量。用荧光标记的echistatin通过荧光显微镜确认其在破骨细胞中的存在。细胞化学方面,使用抗酒石酸酸性磷酸酶来量化成熟和定型的破骨细胞。Echistatin定位于牙周组织中的靶向细胞。
Echistatin显著降低了牙根吸收表面积(P <.01)并减少了牙根吸收陷窝的数量(P <.01)。破骨细胞数量无统计学显著差异。
靶向破牙细胞表达的αvβ3整合素受体可有效减少牙齿移动过程中的牙根吸收。需要进一步研究阐明这种抑制的机制。