The microbial metabolite isovaleric acid aggravates gelatinase‐mediated periodontal tissue destruction via the NF‐κB signaling pathway

IF 4.2 2区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE
Huiling Zheng, Ying Tu, Xinjie Ning, Qiang Guo, Biao Ren, Jing Xie, Chengcheng Liu
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引用次数: 0

Abstract

BackgroundIsovaleric acid, an important short‐chain fatty acid, can be generated by subgingival microbial fermentation of a leucine‐rich diet, such as Porphyromonas gingivalis. This study aimed to explore the impact of isovaleric acid on the destruction of periodontal tissues and to investigate the underlying mechanisms.MethodsThe level of isovaleric acid in the saliva of clinical subjects was measured via mass spectrometry. Isovaleric acid local injection models in 5‐week‐old male Sprague Dawley rats and an isovaleric acid treatment model of human periodontal ligament stem cells (hPDLSCs) were established to explore the effect of isovaleric acid on periodontal tissue destruction and uncover the underlying mechanisms.ResultsOur study revealed that individuals with gingivitis and periodontitis presented significantly higher salivary levels of isovaleric acid than healthy controls. Local injections of isovaleric acid aggravated periodontal tissue damage and alveolar bone loss in rats. Moreover, isovaleric acid amplified the levels and activities of gelatinases, a process facilitated through the activation of NF‐κB (nuclear factor kappa‐B) signaling. Suppression of the NF‐κB pathway significantly reduced the isovaleric acid‐induced increase in gelatinases.ConclusionsOur findings demonstrate that isovaleric acid aggravates the destruction of periodontal tissue by modulating the levels and activities of gelatinases via the NF‐κB signaling pathway both in vitro and in vivo.Plain Language SummaryPeriodontitis is a chronic inflammatory disease characterized by the destruction of periodontal tissues, with oral bacteria as the progressive frontier. Isovaleric acid, an important short‐chain fatty acid, is a substance produced by oral bacteria during the breakdown of protein‐rich foods. By comparing saliva samples from healthy individuals and patients with periodontal diseases, we found that isovaleric acid levels were 2‒3 times higher in patients with inflamed or damaged periodontal tissue. In this study, we assessed the effects of isovaleric acid on periodontal tissues by injecting isovaleric acid into the gums of rats and treating human periodontal cells with isovaleric acid. We found that isovaleric acid worsened periodontal tissue damage and accelerated bone loss. This process worked through NF‐κB signaling pathway activation, which increased the activity and expression of gelatinases, enzymes that break down periodontal tissues. These findings increase our understanding of the possible involvement of isovaleric acid in the development of periodontitis. Targeting isovaleric acid metabolism may provide new approaches for the treatment or prevention of periodontitis.
微生物代谢物异戊酸通过NF - κB信号通路加重明胶酶介导的牙周组织破坏
二戊酸是一种重要的短链脂肪酸,可以通过富含亮氨酸的饮食(如牙龈卟啉单胞菌)的龈下微生物发酵产生。本研究旨在探讨异戊酸对牙周组织破坏的影响,并探讨其潜在机制。方法采用质谱法测定临床受试者唾液中异戊酸的含量。为了探讨异戊酸对牙周组织破坏的影响并揭示其潜在机制,我们建立了5周龄雄性大鼠局部注射异戊酸模型和异戊酸治疗人牙周韧带干细胞(hPDLSCs)模型。结果牙龈炎和牙周炎患者唾液中异戊酸水平明显高于健康对照组。局部注射异戊酸可加重大鼠牙周组织损伤和牙槽骨丢失。此外,异戊酸可通过活化NF - κB(核因子κB)信号通路,增强明胶酶的水平和活性。抑制NF - κB通路可显著降低异戊酸诱导的明胶酶升高。结论在体外和体内实验中,异戊酸通过NF - κB信号通路调节明胶酶的水平和活性,从而加重了牙周组织的破坏。牙周炎是一种以破坏牙周组织为特征的慢性炎症性疾病,以口腔细菌为进展前沿。异戊酸是一种重要的短链脂肪酸,是口腔细菌在分解富含蛋白质的食物时产生的一种物质。通过比较健康人和牙周病患者的唾液样本,我们发现牙周组织发炎或受损的患者的异戊酸水平高出2-3倍。本研究通过在大鼠牙龈内注射异戊酸和用异戊酸治疗人牙周细胞来评估异戊酸对牙周组织的影响。我们发现异戊酸加重牙周组织损伤,加速骨质流失。这一过程通过激活NF‐κB信号通路,增加明胶酶的活性和表达,明胶酶是分解牙周组织的酶。这些发现增加了我们对异戊酸可能参与牙周炎发展的理解。靶向异戊酸代谢可能为牙周炎的治疗或预防提供新的途径。
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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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