Zhu Ningxin, Chatzistavrou Xanthippi, Papagerakis Petros, Ge Lihong, Qin Man, Wang Yuanyuan
Department of Pediatric Dentistry, School and Hospital of Stomatology, Peking University, #22 Zhongguancun Nandajie, Haidian District, Beijing 100081, China.
Department of Chemical Engineering and Materials Science, Michigan State University, East Lansing, Michigan 48824, United States.
ACS Biomater Sci Eng. 2019 Sep 9;5(9):4624-4633. doi: 10.1021/acsbiomaterials.9b00811. Epub 2019 Jul 29.
The major indications of a successful inflamed-pulp-capping procedure are the formation of a dense calcified dentin barrier and the preservation of healthy pulp tissue concomitant with elimination of inflammation. Our aim is to evaluate the effects of an injectable silver-doped bioactive glass/chitosan hydrogel (Ag-BG/CS), as a pulp-capping material, and explore the molecular mechanisms of Ag-BG/CS in regards to its bioactive and anti-inflammatory properties. First, the structure and component of the material were analyzed by scanning electron microscopy. Then, the downstream molecular mechanisms and anti-inflammatory effects were characterized by quantitative polymerase chain reaction (qPCR) and Western blot. Finally, a preclinical model of rat pulpitis was used to explore the potential of Ag-BG/CS in controlling pulp inflammation . The results showed that Ag-BG/CS induced stronger reparative dentin formation and enhanced preservation of vital pulp tissue when compared to the mineral trioxide aggregate (MTA) which is the currently used clinical standard. Ag-BG/CS also significantly increased the phosphorylation of p38 and ERK1/2(p42/44) of dental pulp cells, indicating that Ag-BG/CS enhanced pulpal repair through the mitogen-activated protein kinase (MAPK) pathway. This novel material may represent a superior solution for dental pulp-capping clinical scenarios with specific advantages for cases of early diffuse pulpitis in immature permanent teeth.
成功的牙髓盖髓术的主要指征是形成致密的钙化牙本质屏障,并在消除炎症的同时保留健康的牙髓组织。我们的目的是评估可注射的银掺杂生物活性玻璃/壳聚糖水凝胶(Ag-BG/CS)作为盖髓材料的效果,并探讨Ag-BG/CS在生物活性和抗炎特性方面的分子机制。首先,通过扫描电子显微镜分析材料的结构和成分。然后,通过定量聚合酶链反应(qPCR)和蛋白质免疫印迹法(Western blot)对下游分子机制和抗炎作用进行表征。最后,使用大鼠牙髓炎的临床前模型来探索Ag-BG/CS在控制牙髓炎症方面的潜力。结果表明,与目前临床使用的标准矿物三氧化物凝聚体(MTA)相比,Ag-BG/CS诱导更强的修复性牙本质形成,并增强了牙髓组织的活力保存。Ag-BG/CS还显著增加了牙髓细胞中p38和ERK1/2(p42/44)的磷酸化,表明Ag-BG/CS通过丝裂原活化蛋白激酶(MAPK)途径增强牙髓修复。这种新型材料可能是牙髓盖髓临床情况的一种更优解决方案,对于未成熟恒牙早期弥漫性牙髓炎病例具有特定优势。