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阿仑膦酸钠对幼年生长大鼠牙齿萌出和磨牙牙根形成的影响。

Effects of alendronate on tooth eruption and molar root formation in young growing rats.

作者信息

Bradaschia-Correa Vivian, Massa Luciana F, Arana-Chavez Victor E

机构信息

Laboratory of Mineralized Tissue Biology, Department of Cell and Developmental Biology, Institute of Biomedical Sciences, University of São Paulo, 05508-900 São Paulo, Brazil.

出版信息

Cell Tissue Res. 2007 Dec;330(3):475-85. doi: 10.1007/s00441-007-0499-y. Epub 2007 Sep 28.

Abstract

Tooth eruption consists of the movement of teeth from the bony crypt in which they initiate their development to the occlusal plane in the oral cavity. Interactions between the tooth germ and its surrounding alveolar bone occur in order to offer spatial conditions for its development and eruption. This involves bone remodeling during which resorption is a key event. Bisphosphonates are a group of drugs that interfere with the resorption of mineralized tissues. With the purpose of investigating the effects of sodium alendronate (a potent bisphosphonate inhibitor of osteoclast activity) on alveolar bone during tooth development and eruption, we gave newborn rats daily doses of this drug for 4, 14, and 30 days. Samples of the maxillary alveolar process containing the tooth germs were processed for light, transmission, and scanning electron microscopy and were also submitted to tartrate-resistant acid phosphatase histochemistry and high-resolution colloidal-gold immunolabeling for osteopontin. Inhibition of osteoclast activity by sodium alendronate caused the absence of tooth eruption. The lack of alveolar bone remodeling resulted in primary bone with the presence of latent osteoclasts and abundant osteopontin at the interfibrillar regions. The developing bone trabeculae invaded the dental follicle and reached the molar tooth germs, provoking deformities in enamel surfaces. No root formation was observed. These findings suggested that alendronate effectively inhibited tooth eruption by interfering with the activation of osteoclasts, which remained in a latent stage.

摘要

牙齿萌出是指牙齿从其开始发育的骨隐窝移动到口腔咬合平面的过程。牙胚与其周围牙槽骨之间会发生相互作用,以便为其发育和萌出提供空间条件。这涉及到骨重塑,其中吸收是一个关键事件。双膦酸盐是一类干扰矿化组织吸收的药物。为了研究阿仑膦酸钠(一种有效的破骨细胞活性双膦酸盐抑制剂)在牙齿发育和萌出过程中对牙槽骨的影响,我们给新生大鼠连续4天、14天和30天每日服用该药物。对上颌牙槽突含有牙胚的样本进行光镜、透射电镜和扫描电镜处理,并进行抗酒石酸酸性磷酸酶组织化学和骨桥蛋白的高分辨率胶体金免疫标记。阿仑膦酸钠抑制破骨细胞活性导致牙齿萌出缺失。牙槽骨重塑的缺乏导致初级骨中存在潜伏破骨细胞以及纤维间区域有丰富的骨桥蛋白。发育中的骨小梁侵入牙囊并到达磨牙牙胚,导致釉质表面畸形。未观察到牙根形成。这些发现表明,阿仑膦酸钠通过干扰处于潜伏阶段的破骨细胞的激活而有效抑制牙齿萌出。

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