Qin Ran, Sun Jinyu, Wu Jun, Chen Lulu
Department of Anatomy, Histology and Embryology, Nanjing Medical University Nanjing, Jiangsu, People's Republic of China.
Key Laboratory for Aging and Disease, Nanjing Medical University Nanjing, Jiangsu, People's Republic of China.
Am J Transl Res. 2019 Mar 15;11(3):1460-1472. eCollection 2019.
Accumulating evidence suggests that oxidative stress plays an important role in the progression of osteoarthritis (OA), and pyrroloquinoline quinone (PQQ) is considered a strong antioxidant. However, it is unclear whether PQQ can prevent the progression of OA by inhibiting oxidative stress. In this study, anterior cruciate ligament transection (ACLT)-induced OA mice received a diet supplemented with/without PQQ, and were compared with each other and with sham-operated mice. Our results showed that in PQQ-untreated OA mice, articular surfaces collapsed, while the thickness of articular cartilage and the abundance of cartilage matrix protein decreased significantly, whereas PQQ supplementation largely prevented these alterations. We also found that oxidative stress, DNA damage, cellular senescence and the secretion of senescence-associated inflammatory cytokines were increased in PQQ-untreated OA mice compared with sham-operated mice. However, these parameters were obviously rescued in PQQ-treated OA mice. This study demonstrated that PQQ supplementation can prevent ACLT-induced OA by inhibiting oxidative stress, DNA damage, cell senescence and the development of the senescence-associated secretory phenotype.
越来越多的证据表明,氧化应激在骨关节炎(OA)的进展中起重要作用,而吡咯喹啉醌(PQQ)被认为是一种强大的抗氧化剂。然而,尚不清楚PQQ是否能通过抑制氧化应激来预防OA的进展。在本研究中,前交叉韧带横断(ACLT)诱导的OA小鼠接受添加/不添加PQQ的饮食,并相互比较以及与假手术小鼠进行比较。我们的结果表明,在未用PQQ处理的OA小鼠中,关节表面塌陷,而关节软骨厚度和软骨基质蛋白丰度显著降低,而补充PQQ在很大程度上防止了这些改变。我们还发现,与假手术小鼠相比,未用PQQ处理的OA小鼠的氧化应激、DNA损伤、细胞衰老以及衰老相关炎性细胞因子的分泌增加。然而,这些参数在接受PQQ处理的OA小鼠中明显得到改善。本研究表明,补充PQQ可通过抑制氧化应激、DNA损伤、细胞衰老以及衰老相关分泌表型的发展来预防ACLT诱导的OA。