Tossetta Giovanni, Fantone Sonia, Olivieri Fabiola, Mazzucchelli Roberta, Togni Lucrezia, Santarelli Andrea, Marzioni Daniela, Rippo Maria Rita
Department of Experimental and Clinical Medicine, Università Politecnica delle Marche, Ancona, 60126, Italy.
Department of Biomedical Sciences and Public Health, Section of Pathological Anatomy, Università Politecnica delle Marche, United Hospitals, Ancona, Italy.
Mol Biol Rep. 2025 Jul 30;52(1):771. doi: 10.1007/s11033-025-10878-5.
40% of the population over 60 years of age is affected by periodontitis which is characterized by chronic inflammation, periodontal damage and alveolar bone resorption. The nuclear factor erythroid 2-related factor 2 (NFE2L2 or NRF2)/ Kelch-like ECH-Associated Protein 1 (KEAP1) (NRF2/KEAP1) signaling pathway plays a key role in periodontitis modulating redox balance and periodontium inflammation. However, NRF2 expression decreases in gingival tissues of severe periodontitis patients while Reactive Oxygen Species (ROS) levels are increased during periodontitis. ROS and lipopolysaccharide (LPS) produced by gram-negative bacteria favor the production of inflammatory cytokines, then causing periodontal inflammation and favoring alveolar bone loss (due to excessive osteoclast formation and activation). Periodontitis has also been associated to the development of age-related neurodegenerative diseases such as Alzheimer's and Parkinson's diseases since the increased cytokines levels and the bacteria themselves present in the periodontium can easily reach the brain due to their anatomical proximity. Thus, periodontitis could be considered a risk factor for the development of Alzheimer's and Parkinson's diseases. In this review we explored the role of NRF2/KEAP1 signaling activation in in vitro and in vivo models of periodontitis to suggest potential treatments of periodontitis and avoid/delay the development of age-related neurodegenerative diseases.
60岁以上人群中有40%受到牙周炎影响,其特征为慢性炎症、牙周组织损伤和牙槽骨吸收。核因子红细胞2相关因子2(NFE2L2或NRF2)/ Kelch样ECH相关蛋白1(KEAP1)(NRF2/KEAP1)信号通路在调节牙周炎氧化还原平衡和牙周组织炎症中起关键作用。然而,重度牙周炎患者牙龈组织中NRF2表达降低,而牙周炎期间活性氧(ROS)水平升高。革兰氏阴性菌产生的ROS和脂多糖(LPS)促进炎性细胞因子的产生,进而导致牙周炎症并加剧牙槽骨丧失(由于破骨细胞过度形成和激活)。牙周炎还与年龄相关的神经退行性疾病如阿尔茨海默病和帕金森病的发生有关,因为牙周组织中升高的细胞因子水平和细菌本身由于解剖学上的接近性很容易到达大脑。因此,牙周炎可被视为阿尔茨海默病和帕金森病发生的一个危险因素。在本综述中,我们探讨了NRF2/KEAP1信号激活在牙周炎体外和体内模型中的作用,以提出牙周炎的潜在治疗方法,并避免/延缓年龄相关神经退行性疾病的发生。