Angiotensin(1-7) attenuates tooth movement and regulates alveolar bone response during orthodontic force application in experimental animal model.

IF 4.8 2区 医学 Q1 Dentistry Progress in Orthodontics Pub Date : 2023-10-16 DOI:10.1186/s40510-023-00486-z
Hatem Abuohashish, Suliman Shahin, Abdulaziz Alamri, Zainah Salloot, Hussain Alhawaj, Omar Omar
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Abstract

Background: Renin-angiotensin system and its ACE2/Ang(1-7)/Mas receptor axis regulates skeletal response to multiple physiological and pathological conditions. Recent research suggested a vital role of Ang(1-7) in regulating alveolar bone metabolism and remodeling. In this context, this study evaluated the effects of the Ang(1-7)/Mas receptor axis on orthodontic tooth movement (OTM) and the alveolar bone response to mechanical load.

Methods: A coil spring was placed between the right maxillary first molar and the anterior tooth of Wistar rats to apply bidirectional mechanical force. Ang(1-7) with or without a specific Mas receptor antagonist (A779) was infused using subcutaneous osmotic pumps (200 and 400 ng/kg/min: respectively). Animals were killed after 5 and 14 days from the OTM procedure after the clinical evaluation of tooth movement and mobility. Morphometric analysis of alveolar bone structure was conducted using micro-CT and the histological picture was evaluated after H&E staining. Moreover, collagen fiber distribution was assessed using Picro-Sirius red stain. In addition, bone samples were collected from the pressure and tension sites around the anterior tooth for gene expression analysis.

Results: Ang(1-7) infusion suppressed the tooth movement and mobility after 14 days of the orthodontic force application. Additionally, Ang(1-7) infusion preserved the morphometric and histological structure of the alveolar bone at pressure and tension sides. These effects were abolished by adding A779 infusion. Collagen fiber distribution was dysregulated mainly by the A779 Mas receptor blockage. Ang(1-7) affected the bone formation, remodeling- and vascularity-related genes in the pressure and tension sides, suggesting a prominent suppression of osteoclastogenesis. Ang(1-7) also improved osteoblasts-related genes on the tension side, whereas the osteoclasts-related genes were augmented by A779 on the pressure side.

Conclusion: Collectively, the activation of Ang(1-7)/Mas receptor axis appears to hinder tooth movement and regulates alveolar bone remodeling in response to mechanical force.

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在实验动物模型中,在正畸力施加过程中,血管紧张素(1-7)减弱牙齿运动并调节牙槽骨反应。
背景:肾素-血管紧张素系统及其ACE2/Ang(1-7)/Mas受体轴调节骨骼对多种生理和病理条件的反应。最近的研究表明Ang(1-7)在调节牙槽骨代谢和重塑中起着至关重要的作用。在此背景下,本研究评估了Ang(1-7)/Mas受体轴对正畸牙齿运动(OTM)和牙槽骨对机械负荷的反应的影响。方法:将螺旋弹簧置于Wistar大鼠右上颌第一磨牙与前牙之间,施加双向机械力。使用皮下渗透泵(分别为200和400ng/kg/min)输注具有或不具有特异性Mas受体拮抗剂(A779)的Ang(1-7)。在对牙齿移动和活动性进行临床评估后,在OTM手术后5天和14天处死动物。用显微CT对牙槽骨结构进行形态计量学分析,并在H&E染色后评估组织学图像。此外,使用Picro Sirius红染色评估胶原纤维分布。此外,从前牙周围的压力和张力部位采集骨骼样本,用于基因表达分析。结果:Ang(1-7)可抑制正畸力作用14d后牙齿的移动和活动。此外,Ang(1-7)输注在压力侧和张力侧保留了牙槽骨的形态计量学和组织学结构。通过添加A779输注来消除这些影响。胶原纤维分布失调主要是由于A779Mas受体的阻断。Ang(1-7)影响压力侧和张力侧的骨形成、重塑和血管形成相关基因,表明破骨细胞生成受到显著抑制。Ang(1-7)也改善了张力侧的成骨细胞相关基因,而压力侧的A779增强了破骨细胞相关的基因。结论:Ang(1-7)/Mas受体轴的激活总体上阻碍了牙齿的运动,并调节了牙槽骨对机械力的重塑。
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来源期刊
Progress in Orthodontics
Progress in Orthodontics Dentistry-Orthodontics
CiteScore
7.30
自引率
4.20%
发文量
45
审稿时长
13 weeks
期刊介绍: Progress in Orthodontics is a fully open access, international journal owned by the Italian Society of Orthodontics and published under the brand SpringerOpen. The Society is currently covering all publication costs so there are no article processing charges for authors. It is a premier journal of international scope that fosters orthodontic research, including both basic research and development of innovative clinical techniques, with an emphasis on the following areas: • Mechanisms to improve orthodontics • Clinical studies and control animal studies • Orthodontics and genetics, genomics • Temporomandibular joint (TMJ) control clinical trials • Efficacy of orthodontic appliances and animal models • Systematic reviews and meta analyses • Mechanisms to speed orthodontic treatment Progress in Orthodontics will consider for publication only meritorious and original contributions. These may be: • Original articles reporting the findings of clinical trials, clinically relevant basic scientific investigations, or novel therapeutic or diagnostic systems • Review articles on current topics • Articles on novel techniques and clinical tools • Articles of contemporary interest
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