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局部给予高剂量糖尿病药物艾塞那肽-4可抑制小鼠正畸牙齿移动。

Local administration of high-dose diabetes medicine exendin-4 inhibits orthodontic tooth movement in mice.

作者信息

Shen Wei-Ren, Kitaura Hideki, Qi Jiawei, Ogawa Saika, Ohori Fumitoshi, Noguchi Takahiro, Marahleh Aseel, Nara Yasuhiko, Adya Pramusita, Mizoguchi Itaru

出版信息

Angle Orthod. 2021 Jan 1;91(1):111-118. doi: 10.2319/021320-103.1.

Abstract

OBJECTIVES

To investigate the effects of exendin-4 on orthodontic tooth movement distance, root resorption, and expression levels of osteoclast-related cytokines in a mouse model.

MATERIALS AND METHODS

A 10-g NiTi coil spring was placed between the anterior alveolar bone and upper left first molar of 8-week-old male C57BL/6 mice. Twenty microliters of exendin-4 solution (containing 0.2 μg, 4 μg, or 20 μg exendin-4) or phosphate-buffered saline (PBS) were injected on the buccal side of the upper left first molar at 2-day intervals (4 mice per group). Mice were sacrificed on day 12; silicone impressions were taken to record tooth movement distance. The left maxillae of the PBS and 20 μg exendin-4 groups were also excised for histological analysis and quantitative reverse transcription polymerase chain reaction analysis.

RESULTS

Orthodontic tooth movement distance was smaller in the 20 μg exendin-4 group than in the PBS group (P < .01). Compared with the PBS group, the 20 μg exendin-4 group showed lower osteoclast number (P < .05), odontoclast number (P < .05), and root resorption surface percentage (P < .05). Relative to maxillae with PBS injections, maxillae with 20 μg exendin-4 injections had lower receptor activator of nuclear factor kappa-B ligand (RANKL) mRNA expression (P < .05), TNF-α mRNA expression (P < .05), and RANKL/osteoprotegerin (OPG) ratio (P < .01). There were no differences in the expression of OPG mRNA.

CONCLUSIONS

Exendin-4 inhibits orthodontic tooth movement. Therefore, additional attention is needed for orthodontic patients who receive exendin-4 for diabetes treatment. GLP-1 receptor may be a treatment target for patients with severe root resorption.

摘要

目的

在小鼠模型中研究艾塞那肽-4对正畸牙齿移动距离、牙根吸收以及破骨细胞相关细胞因子表达水平的影响。

材料与方法

将一个10克的镍钛螺旋弹簧置于8周龄雄性C57BL/6小鼠的前牙槽骨与左上第一磨牙之间。每隔2天在左上第一磨牙颊侧注射20微升艾塞那肽-4溶液(含0.2微克、4微克或20微克艾塞那肽-4)或磷酸盐缓冲盐水(PBS)(每组4只小鼠)。在第12天处死小鼠;制取硅橡胶印模以记录牙齿移动距离。还切除PBS组和20微克艾塞那肽-4组的左上颌骨用于组织学分析和定量逆转录聚合酶链反应分析。

结果

20微克艾塞那肽-4组的正畸牙齿移动距离小于PBS组(P < 0.01)。与PBS组相比,20微克艾塞那肽-4组的破骨细胞数量(P < 0.05)、牙破骨细胞数量(P < 0.05)和牙根吸收表面百分比(P < 0.05)更低。相对于注射PBS的上颌骨,注射20微克艾塞那肽-4的上颌骨中核因子κB受体活化因子配体(RANKL)mRNA表达(P < 0.05)、TNF-α mRNA表达(P < 0.05)以及RANKL/骨保护素(OPG)比值(P < 0.01)更低。OPG mRNA的表达无差异。

结论

艾塞那肽-4抑制正畸牙齿移动。因此,对于接受艾塞那肽-4治疗糖尿病的正畸患者需要格外关注。胰高血糖素样肽-1受体可能是严重牙根吸收患者的治疗靶点。

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