Non-Surgical Periodontal Therapy and Metformin Improve Bone Loss in Obese Mice With Periodontitis by Modulating the Gut Microbiota

IF 4.2 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Rixin Chen, Wei Wei, Lili Li, Miaomiao Zhang, Nannan Wang, Ruiyang Ge, Yue Shen, Wen Zhang, Daiyv Lu, Wenzheng Liao, Yanfen Li, Fuhua Yan
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Abstract

Periodontitis and obesity are chronic inflammatory diseases associated with osteoporosis. Controlling inflammation is crucial for managing periodontitis in individuals with obesity. Metformin has shown potent anti-inflammatory effects under inflammatory conditions. However, the effects of adjunctive systemic administration of metformin alongside non-surgical periodontal therapy (NSPT) on periodontal and systemic bone health in obesity remain unknown. In this study, a high-fat diet (HFD)-induced obese murine model was created with periodontitis through ligation. Periodontal treatment consisted of standard mechanical debridement via NSPT, with or without metformin treatment through oral gavage. Outcomes were evaluated based on changes in periodontal status, systemic bone resorption and inflammation, as well as the gut microbiota community and metabolism. Our results indicated that periodontitis significantly increased osteoclastic activity and resulted in alveolar and femoral bone loss in HFD-fed mice. Compared to NSPT alone, NSPT and metformin significantly improved periodontitis, reduced systemic inflammation, and alleviated femoral bone absorption in HFD-fed mice. Mechanistically, periodontitis promoted gut microbiota dysbiosis and disrupted microbial linoleic acid metabolism. NSPT and metformin normalized the gut microbiota, enhanced the growth of species with anti-inflammatory properties, including Faecalibacterium prausnitzii, Akkermansia muciniphila, Lactobacillus reuteri, and Butyricicoccus pullicaecorum, and restored the balance of linoleic acid metabolism in the gut and serum. This research presents novel evidence that metformin may serve as a promising adjunct to enhance the response of obese subjects to NSPT by regulating the gut microbiota and linoleic acid metabolism, indicating that the gut microbiota could be a potential therapeutic target for multidisciplinary intervention in periodontitis and obesity.

Abstract Image

非手术牙周治疗和二甲双胍通过调节肠道微生物群改善患有牙周炎的肥胖小鼠的骨质流失
牙周炎和肥胖是与骨质疏松症相关的慢性炎症性疾病。控制炎症对于治疗肥胖患者的牙周炎至关重要。二甲双胍在炎症条件下显示出有效的抗炎作用。然而,辅助全身给予二甲双胍与非手术牙周治疗(NSPT)对肥胖患者牙周和全身骨骼健康的影响尚不清楚。本研究采用结扎法建立高脂饮食(HFD)诱导的肥胖小鼠牙周炎模型。牙周治疗包括通过NSPT进行标准机械清创,通过口服灌胃给予或不给予二甲双胍治疗。结果评估基于牙周状态,全身骨吸收和炎症,以及肠道微生物群落和代谢的变化。我们的研究结果表明,牙周炎显著增加破骨细胞活性,导致hfd喂养小鼠的牙槽骨和股骨骨丢失。与单独使用NSPT相比,NSPT和二甲双胍显著改善了hfd喂养小鼠的牙周炎,减轻了全身炎症,减轻了股骨吸收。从机制上讲,牙周炎促进肠道菌群失调,破坏微生物亚油酸代谢。NSPT和二甲双胍使肠道菌群正常化,促进了具有抗炎特性的菌种的生长,包括prausnitzii Faecalibacterium、Akkermansia muciniphila、reuteri乳杆菌和pullicaecorum丁酸球菌,并恢复了肠道和血清中亚油酸代谢的平衡。本研究提供了新的证据,表明二甲双胍可能通过调节肠道微生物群和亚油酸代谢来增强肥胖受试者对NSPT的反应,这表明肠道微生物群可能是牙周炎和肥胖多学科干预的潜在治疗靶点。
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来源期刊
The FASEB Journal
The FASEB Journal 生物-生化与分子生物学
CiteScore
9.20
自引率
2.10%
发文量
6243
审稿时长
3 months
期刊介绍: The FASEB Journal publishes international, transdisciplinary research covering all fields of biology at every level of organization: atomic, molecular, cell, tissue, organ, organismic and population. While the journal strives to include research that cuts across the biological sciences, it also considers submissions that lie within one field, but may have implications for other fields as well. The journal seeks to publish basic and translational research, but also welcomes reports of pre-clinical and early clinical research. In addition to research, review, and hypothesis submissions, The FASEB Journal also seeks perspectives, commentaries, book reviews, and similar content related to the life sciences in its Up Front section.
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