Tang Genxiong, Ma Haoran, Liu Shuying, Wu Jun, Gong Aixiu
Department of Stomatology, Children's Hospital of Nanjing Medical University Nanjing 210008, Jiangsu, China.
State Key Laboratory of Reproductive Medicine, Center for Bone and Stem Cells, Department of Anatomy, Histology and Embryology, Nanjing Medical University Nanjing 210029, Jiangsu, China.
Am J Transl Res. 2022 Jan 15;14(1):582-593. eCollection 2022.
It has been demonstrated that oxidative stress is related to periodontitis, and that pyrroloquinoline quinine (PQQ) acts as a powerful antioxidant. This study aimed to explore the effect of PQQ on ligature-induced alveolar bone loss in experimental periodontitis (EP) mice with/without PQQ in the diet. EP mice received a diet supplemented with PQQ for 2 weeks and were compared with sham (control) mice as well as untreated EP mice. Additionally, human periodontal ligament cells (hPDLCs) were treated with PQQ in the presence or absence of lipopolysaccharide (LPS). We found that the bone volume fraction, alkaline phosphatase activity, and the number of antioxidant cells were significantly decreased in EP mice compared with the sham mice, whereas PQQ administration rescued the above effects. In contrast, alveolar bone loss, osteoclast number, cell senescence-associated cells, and cytokines' expression were significantly increased in EP mice compared with the sham mice but were significantly decreased with PQQ supplementation in periodontal tissues. Furthermore, we found that antioxidant enzymes and Bmi-1 protein expression levels were downregulated, whereas the protein expression levels of cell senescence-related proteins including γ-H2AX, IL-6, IL-1β, p16, and p21 were significantly up-regulated in LPS-induced hPDLCs compared with the control cells. However, PQQ administration partially prevented these changes. These findings suggest that PQQ may alleviate periodontal damage through regulation of the redox balance and cell senescence.
已有研究表明,氧化应激与牙周炎相关,而吡咯喹啉醌(PQQ)是一种强大的抗氧化剂。本研究旨在探讨饮食中添加或不添加PQQ对实验性牙周炎(EP)小鼠结扎诱导的牙槽骨丢失的影响。EP小鼠接受添加PQQ的饮食2周,并与假手术(对照)小鼠以及未治疗的EP小鼠进行比较。此外,在有或没有脂多糖(LPS)的情况下,用人牙周膜细胞(hPDLCs)进行PQQ处理。我们发现,与假手术小鼠相比,EP小鼠的骨体积分数、碱性磷酸酶活性和抗氧化细胞数量显著降低,而给予PQQ可挽救上述影响。相反,与假手术小鼠相比,EP小鼠的牙槽骨丢失、破骨细胞数量、细胞衰老相关细胞和细胞因子表达显著增加,但在牙周组织中补充PQQ后显著降低。此外,我们发现与对照细胞相比,LPS诱导的hPDLCs中抗氧化酶和Bmi-1蛋白表达水平下调,而包括γ-H2AX、IL-6、IL-1β、p16和p21在内的细胞衰老相关蛋白的蛋白表达水平显著上调。然而,给予PQQ可部分预防这些变化。这些发现表明,PQQ可能通过调节氧化还原平衡和细胞衰老来减轻牙周损伤。