Viglianisi Gaia, Tartaglia Gianluca Martino, Santonocito Simona, Amato Mariacristina, Polizzi Alessandro, Mascitti Marco, Isola Gaetano
Department of General Surgery and Surgical-Medical Specialties, School of Dentistry, University of Catania, Via S. Sofia 78, 95124 Catania, Italy.
Section of Maxillo-Facial Surgery and Dentistry Fondazione IRCCS Cà Granda, Ospedale Maggiore Policlinico, Department of Orthodontics, School of Dentistry, University of Milan, 20122 Milan, Italy.
J Pers Med. 2023 Jan 17;13(2):166. doi: 10.3390/jpm13020166.
Periodontitis is a multifactorial and infective oral disease that leads to the destruction of periodontal tissues and tooth loss. Although the treatment of periodontitis has improved recently, the effective treatment of periodontitis and the periodontitis-affected periodontal tissues is still a challenge. Therefore, exploring new therapeutic strategies for a personalized approach is urgent. For this reason, the aim of this study is to summarize recent advances and the potential of oxidative stress biomarkers in the early diagnosis and personalized therapeutic approaches in periodontitis. Recently, ROS metabolisms (ROMs) have been studied in the physiopathology of periodontitis. Different studies show that ROS plays a crucial role in periodontitis. In this regard, the reactive oxygen metabolites (ROMs) started to be searched for the measures of the oxidizing capacity of the plasma understood as the total content of oxygen free radicals (ROS). The oxidizing capacity of plasma is a significant indicator of the body's oxidant state as well as homocysteine (Hcy), sulfur amino acid, which has pro-oxidant effects as it favors the production of superoxide anion. More specifically, the thioredoxin (TRX) and peroxiredoxin (PRX) systems control reactive oxygen species (ROS), such as superoxide and hydroxyl species, to transduce redox signals and change the activities of antioxidant enzymes to remove free radicals. Superoxide dismutase (SOD), catalase, and glutathione peroxidase (GPx), among other antioxidant enzymes, change their activity when ROS are produced in order to neutralize free radicals. The TRX system is triggered and transduces redox signals to do this.
牙周炎是一种多因素感染性口腔疾病,可导致牙周组织破坏和牙齿脱落。尽管近年来牙周炎的治疗有所改善,但有效治疗牙周炎以及受牙周炎影响的牙周组织仍然是一项挑战。因此,探索个性化的新治疗策略迫在眉睫。出于这个原因,本研究的目的是总结氧化应激生物标志物在牙周炎早期诊断和个性化治疗方法方面的最新进展及潜力。最近,活性氧代谢(ROMs)已在牙周炎的生理病理学中得到研究。不同的研究表明,活性氧在牙周炎中起着关键作用。在这方面,开始寻找活性氧代谢产物(ROMs)作为血浆氧化能力的指标,血浆氧化能力被理解为氧自由基(ROS)的总含量。血浆氧化能力是身体氧化状态的重要指标,同型半胱氨酸(Hcy)这种含硫氨基酸也一样,它具有促氧化作用,因为它有利于超氧阴离子的产生。更具体地说,硫氧还蛋白(TRX)和过氧化物氧还蛋白(PRX)系统控制超氧和羟基等活性氧(ROS),以转导氧化还原信号并改变抗氧化酶的活性来清除自由基。超氧化物歧化酶(SOD)、过氧化氢酶和谷胱甘肽过氧化物酶(GPx)等其他抗氧化酶在产生ROS时会改变其活性以中和自由基。TRX系统被触发并转导氧化还原信号来实现这一点。