• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Local administration of high-dose diabetes medicine exendin-4 inhibits orthodontic tooth movement in mice.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。
Angle Orthod. 2021 Jan 1;91(1):111-118. doi: 10.2319/021320-103.1.
2
Effect of a DPP-4 Inhibitor on Orthodontic Tooth Movement and Associated Root Resorption.二肽基肽酶-4 抑制剂对正畸牙齿移动及相关牙根吸收的影响。
Biomed Res Int. 2020 Aug 18;2020:7189084. doi: 10.1155/2020/7189084. eCollection 2020.
3
Expression of mRNA for osteoprotegerin and receptor activator of nuclear factor kappa beta ligand (RANKL) during root resorption induced by the application of heavy orthodontic forces on rat molars.大鼠磨牙施加重度正畸力诱导牙根吸收过程中骨保护素及核因子κB受体活化因子配体(RANKL)mRNA的表达
Am J Orthod Dentofacial Orthop. 2005 Oct;128(4):497-503. doi: 10.1016/j.ajodo.2004.03.038.
4
Effect of TNF--Induced Sclerostin on Osteocytes during Orthodontic Tooth Movement.TNF-α诱导骨钙素蛋白在正畸牙齿移动过程中对破骨细胞的作用。
J Immunol Res. 2019 Jun 24;2019:9716758. doi: 10.1155/2019/9716758. eCollection 2019.
5
Mechanical force regulates root resorption in rats through RANKL and OPG.机械力通过 RANKL 和 OPG 调节大鼠的牙根吸收。
BMC Oral Health. 2022 Jul 16;22(1):290. doi: 10.1186/s12903-022-02327-7.
6
Influence of bisphosphonates on orthodontic tooth movement in mice.双磷酸盐对小鼠正畸牙齿移动的影响。
Eur J Orthod. 2009 Dec;31(6):572-7. doi: 10.1093/ejo/cjp068. Epub 2009 Oct 19.
7
Osteoclast induction in periodontal tissue during experimental movement of incisors in osteoprotegerin-deficient mice.骨保护素缺乏小鼠切牙实验性移动过程中牙周组织中的破骨细胞诱导
Anat Rec. 2002 Apr 1;266(4):218-25. doi: 10.1002/ar.10061.
8
Receptor activator of nuclear factor-kappa ligand, OPG, and IGF-I expression during orthodontically induced inflammatory root resorption in the recombinant human growth hormone-treated rats.重组人生长激素治疗大鼠正畸诱导性炎性牙根吸收过程中核因子κB受体激活剂、骨保护素及胰岛素样生长因子-I的表达
Angle Orthod. 2015 Jul;85(4):562-9. doi: 10.2319/052014-361.1. Epub 2014 Sep 3.
9
Microsphere controlled drug delivery for local control of tooth movement.用于局部控制牙齿移动的微球控释给药
Eur J Orthod. 2019 Jan 23;41(1):1-8. doi: 10.1093/ejo/cjy017.
10
Expressions of RANKL/RANK and M-CSF/c-fms in root resorption lacunae in rat molar by heavy orthodontic force.正畸力作用下大鼠磨牙牙根吸收陷窝中 RANKL/RANK 和 M-CSF/c-fms 的表达
Eur J Orthod. 2011 Aug;33(4):335-43. doi: 10.1093/ejo/cjq068. Epub 2010 Sep 10.

引用本文的文献

1
Docosahexaenoic acid inhibits TNF-α-induced osteoclast formation and orthodontic tooth movement through GPR120.二十二碳六烯酸通过 GPR120 抑制 TNF-α 诱导的破骨细胞形成和正畸牙齿移动。
Front Immunol. 2023 Jan 18;13:929690. doi: 10.3389/fimmu.2022.929690. eCollection 2022.
2
Effects of anti-mouse RANKL antibody on orthodontic tooth movement in mice.抗小鼠RANKL抗体对小鼠正畸牙齿移动的影响。
J Dent Sci. 2022 Jul;17(3):1087-1095. doi: 10.1016/j.jds.2022.02.007. Epub 2022 Feb 28.
3
Enhancement of orthodontic tooth movement and root resorption in ovariectomized mice.去卵巢小鼠正畸牙齿移动和牙根吸收的增强
J Dent Sci. 2022 Apr;17(2):984-990. doi: 10.1016/j.jds.2021.11.009. Epub 2021 Dec 2.
4
Tumor necrosis factor-α enhances the expression of vascular endothelial growth factor in a mouse orthodontic tooth movement model.肿瘤坏死因子-α在小鼠正畸牙移动模型中增强血管内皮生长因子的表达。
J Dent Sci. 2022 Jan;17(1):415-420. doi: 10.1016/j.jds.2021.08.011. Epub 2021 Sep 1.
5
Effects of Incretin-Related Diabetes Drugs on Bone Formation and Bone Resorption.肠促胰岛素相关糖尿病药物对骨形成和骨吸收的影响。
Int J Mol Sci. 2021 Jun 19;22(12):6578. doi: 10.3390/ijms22126578.

本文引用的文献

1
The global epidemics of diabetes in the 21st century: Current situation and perspectives.21 世纪全球糖尿病流行:现状与展望。
Eur J Prev Cardiol. 2019 Dec;26(2_suppl):7-14. doi: 10.1177/2047487319881021.
2
TNF-α is responsible for the contribution of stromal cells to osteoclast and odontoclast formation during orthodontic tooth movement.TNF-α 负责在正畸牙齿移动过程中基质细胞对破骨细胞和破牙细胞形成的贡献。
PLoS One. 2019 Oct 16;14(10):e0223989. doi: 10.1371/journal.pone.0223989. eCollection 2019.
3
Exendin-4 regulates Wnt and NF-κB signaling in lipopolysaccharide-induced human periodontal ligament stem cells to promote osteogenic differentiation.Exendin-4 通过调节脂多糖诱导的人牙周膜干细胞中的 Wnt 和 NF-κB 信号通路促进成骨分化。
Int Immunopharmacol. 2019 Oct;75:105801. doi: 10.1016/j.intimp.2019.105801. Epub 2019 Aug 8.
4
The GLP-1 Receptor Agonist Exenatide Ameliorates Bone Composition and Tissue Material Properties in High Fat Fed Diabetic Mice.胰高血糖素样肽-1受体激动剂艾塞那肽改善高脂喂养糖尿病小鼠的骨成分和组织材料特性。
Front Endocrinol (Lausanne). 2019 Feb 12;10:51. doi: 10.3389/fendo.2019.00051. eCollection 2019.
5
Glucagon-like peptide-1 receptor agonists and fracture risk: a network meta-analysis of randomized clinical trials.胰高血糖素样肽-1 受体激动剂与骨折风险:一项随机临床试验的网络荟萃分析。
Osteoporos Int. 2018 Dec;29(12):2639-2644. doi: 10.1007/s00198-018-4649-8. Epub 2018 Aug 6.
6
The Glucagon-Like Peptide-1 Receptor Agonist Exendin-4 Inhibits Lipopolysaccharide-Induced Osteoclast Formation and Bone Resorption via Inhibition of TNF- Expression in Macrophages.胰高血糖素样肽-1 受体激动剂 exendin-4 通过抑制巨噬细胞中 TNF- 的表达抑制脂多糖诱导的破骨细胞形成和骨吸收。
J Immunol Res. 2018 Mar 13;2018:5783639. doi: 10.1155/2018/5783639. eCollection 2018.
7
RANKL deletion in periodontal ligament and bone lining cells blocks orthodontic tooth movement.牙周韧带和骨衬细胞中 RANKL 的缺失可阻止正畸牙齿移动。
Int J Oral Sci. 2018 Feb 26;10(1):3. doi: 10.1038/s41368-017-0004-8.
8
Exenatide exhibits anti-inflammatory properties and modulates endothelial response to tumor necrosis factor α-mediated activation.艾塞那肽具有抗炎特性,并调节内皮细胞对肿瘤坏死因子 α 介导的激活的反应。
Cardiovasc Ther. 2018 Apr;36(2). doi: 10.1111/1755-5922.12317. Epub 2018 Jan 24.
9
Exendin-4 Induces Bone Marrow Stromal Cells Migration Through Bone Marrow-Derived Macrophages Polarization via PKA-STAT3 Signaling Pathway.艾塞那肽-4通过蛋白激酶A-信号转导和转录激活因子3信号通路诱导骨髓来源的巨噬细胞极化,从而促进骨髓基质细胞迁移。
Cell Physiol Biochem. 2017;44(5):1696-1714. doi: 10.1159/000485776. Epub 2017 Dec 6.
10
Exenatide Improves Bone Quality in a Murine Model of Genetically Inherited Type 2 Diabetes Mellitus.艾塞那肽改善遗传性2型糖尿病小鼠模型的骨质量。
Front Endocrinol (Lausanne). 2017 Nov 20;8:327. doi: 10.3389/fendo.2017.00327. eCollection 2017.

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.

DOI:10.2319/021320-103.1
PMID:33289799
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8032283/
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。