Metformin reverses periodontal destruction caused by experimental periodontitis by inhibiting interleukin-1β activity.

IF 4.2 2区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE
Zhao Wang, Ju Han Song, Jung-Woo Kim, Seung-Hee Kwon, Xianyu Piao, Sin-Hye Oh, Suk-Gyun Park, Sun-Hun Kim, Je-Hwang Ryu, Ok-Su Kim, Jeong-Tae Koh
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引用次数: 0

Abstract

Background: Periodontitis is a destructive disease that affects periodontal tissue. While current research focuses on disease management, research on tissue repair remains limited. Metformin, a first-line medication for diabetes treatment, has positive effects on bone health in nondiabetic patients. However, its potential for repairing periodontal tissue remains unclear. Therefore, this study aimed to evaluate the reparative effects of metformin on periodontitis-damaged periodontal tissue in mice.

Methods: A mouse model of periodontal repair was used, in which silk ligatures were removed from the molars after inducing periodontitis, followed by metformin administration. Histomorphometric and histological analyses were conducted to assess comprehensive repair of the periodontium. Additional in vitro studies were conducted to determine the effect of metformin on the function of the individual cells that comprise the periodontium.

Results: Metformin treatment promoted the repair of periodontal ligament, alveolar bone, and cementum affected by periodontitis, as evaluated using microcomputed tomography based morphometric and histologic analyses. The therapeutic effect was linked to mitigating persistent inflammatory activity during periodontitis resolution, primarily attributed to the sustained presence of interleukin-1 beta (IL-1β), which may delay tissue repair. In vitro studies simulating this pathological condition showed that AMP-activated protein kinase (AMPK) activation by metformin counteracted the effect of IL-1β, inhibited osteoclast differentiation and restored the osteogenic differentiation capacity of periodontal ligament cells and cementoblasts.

Conclusion: These findings suggest that metformin holds promise for repairing periodontal tissue following periodontitis, potentially through modulating inflammatory responses and regulating cellular differentiation processes.

Plain language summary: Periodontitis is a serious gum disease that destroys the structures that support the teeth, such as ligaments and bone. While current treatments focus on preventing further damage, little progress has been made in achieving complete restoration of damaged tissue. In this study, we investigated whether metformin, a common diabetes drug, could help repair periodontal tissue. Using a mouse model of periodontitis, we removed ligatures placed around the teeth to allow healing, followed by metformin treatment. Our results showed that metformin promoted the repair of key tissues such as the periodontal ligament, alveolar bone, and cementum. An important observation in this study is the persistence of inflammatory activity during periodontitis resolution, where prolonged inflammation, driven by molecules such as interleukin-1β (IL-1β), appears to hinder tissue recovery. Metformin was found to counteract prolonged inflammation by reducing IL-1β activity, allowing tissue to heal. It also restored the function of bone-forming cells and limited the activity of bone-resorbing cells. These results suggest that metformin may be a promising therapy for promoting periodontal tissue repair by both controlling inflammation and enhancing cellular activity critical for tissue restoration.

背景:牙周炎是一种影响牙周组织的破坏性疾病:牙周炎是一种影响牙周组织的破坏性疾病。目前的研究主要集中在疾病管理方面,而对组织修复的研究仍然有限。二甲双胍是治疗糖尿病的一线药物,对非糖尿病患者的骨骼健康有积极影响。然而,其修复牙周组织的潜力仍不明确。因此,本研究旨在评估二甲双胍对小鼠牙周炎受损牙周组织的修复作用:方法:采用小鼠牙周修复模型,在诱发牙周炎后从臼齿上取下丝线结扎,然后服用二甲双胍。进行了组织形态计量学和组织学分析,以评估牙周的全面修复情况。另外还进行了体外研究,以确定二甲双胍对构成牙周的单个细胞功能的影响:结果:二甲双胍治疗促进了受牙周炎影响的牙周韧带、牙槽骨和牙骨质的修复。这种治疗效果与缓解牙周炎缓解过程中的持续炎症活动有关,这主要归因于白细胞介素-1β(IL-1β)的持续存在,而白细胞介素-1β可能会延迟组织修复。模拟这种病理条件的体外研究表明,二甲双胍激活的AMP激活蛋白激酶(AMPK)可以抵消IL-1β的作用,抑制破骨细胞的分化,恢复牙周韧带细胞和骨水泥母细胞的成骨分化能力:这些研究结果表明,二甲双胍有望通过调节炎症反应和细胞分化过程来修复牙周炎后的牙周组织。虽然目前的治疗方法侧重于防止进一步的损害,但在实现受损组织的完全修复方面进展甚微。在这项研究中,我们探讨了二甲双胍这种常见的糖尿病药物是否有助于修复牙周组织。我们使用小鼠牙周炎模型,移除放置在牙齿周围的结扎以促进愈合,然后进行二甲双胍治疗。结果显示,二甲双胍促进了牙周韧带、牙槽骨和骨水泥等关键组织的修复。这项研究的一个重要发现是,在牙周炎消退过程中,炎症活动持续存在,在白细胞介素-1β(IL-1β)等分子的驱动下,炎症长期存在似乎阻碍了组织的恢复。研究发现,二甲双胍可通过降低IL-1β的活性来对抗长期炎症,使组织得以愈合。它还能恢复骨形成细胞的功能,限制骨吸收细胞的活性。这些结果表明,二甲双胍既能控制炎症,又能增强对组织修复至关重要的细胞活性,可能是一种促进牙周组织修复的有效疗法。
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来源期刊
Journal of periodontology
Journal of periodontology 医学-牙科与口腔外科
CiteScore
9.10
自引率
7.00%
发文量
290
审稿时长
3-8 weeks
期刊介绍: The Journal of Periodontology publishes articles relevant to the science and practice of periodontics and related areas.
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