Department of Restorative Dentistry, Universidade Federal de Minas Gerais (UFMG), School of Dentistry, Belo Horizonte-MG, Brazil.
Department of Restorative Dentistry, São Paulo State University (UNESP), School of Dentistry, Araçatuba-SP, Brazil.
Int Endod J. 2024 May;57(5):586-600. doi: 10.1111/iej.14033. Epub 2024 Feb 7.
To evaluate the influence of an experimental solution of cobalt-doped F18 bioactive glass (F18Co) on tissue repair following regenerative endodontic procedure (REP) in rat molars.
The F18Co solution was prepared at a ratio of 1:5 F18Co powder to distilled water. The right or left upper first molars of 12 Wistar rats were used, where the pulps were exposed, removed, and irrigated with 2.5% sodium hypochlorite (NaOCl), followed by 17% ethylenediaminetetraacetic acid (EDTA) (5 min each). Subsequently, the molars were divided into two groups (n = 6): REP-SS and REP-F18Co, where they received a final irrigation (5 min) with saline solution (SS) or F18Co solution, respectively. Then, intracanal bleeding was induced, and the tooth was sealed. Untreated molars were used as controls (n = 3). At 21 days, the rats were euthanized, and the specimens were processed for analysis of mineralized tissue and soft tissue formation inside the root canal using haematoxylin-eosin. The presence and maturation of collagen were evaluated by Masson's trichrome and picrosirius red staining. Immunolabelling analyses of proliferating cell nuclear antigen (PCNA) and osteocalcin (OCN) were performed. The data were submitted to the Mann-Whitney U-test (p < .05).
There was a similar formation of mineralized tissue in thickness and length in REP-SS and REP-F18Co groups (p > .05). Regarding the presence of newly formed soft tissue, most specimens of the REP-F18Co had tissue formation up to the cervical third of the canal, whilst the REP-SS specimens showed formation up to the middle third (p < .05), and there was higher maturation of collagen in REP-F18Co (p < .05). The number of PCNA-positive cells found in the apical third of the root canal was significantly higher in the F18Co group, as well as the OCN immunolabelling, which was severe in most specimens of REP-F18Co, and low in most specimens of REP-SS.
The final irrigation with F18Co bioactive glass solution in REP did not influence mineralized tissue formation but induced soft tissue formation inside the root canals, with higher collagen maturation, and an increase in PCNA-positive cells and OCN immunolabelling.
评估钴掺杂 F18 生物活性玻璃(F18Co)实验溶液对再生牙髓治疗(REP)后大鼠磨牙组织修复的影响。
F18Co 溶液按 1:5 F18Co 粉末与蒸馏水的比例制备。使用 12 只 Wistar 大鼠的右上或左上第一磨牙,暴露牙髓,用 2.5%次氯酸钠(NaOCl)去除,然后用 17%乙二胺四乙酸(EDTA)冲洗(各 5 分钟)。随后,将磨牙分为两组(n=6):REP-SS 和 REP-F18Co,分别用生理盐水(SS)或 F18Co 溶液进行最后冲洗(5 分钟)。然后,诱导根管内出血,并密封牙齿。未处理的磨牙作为对照(n=3)。21 天后,处死大鼠,对标本进行苏木精-伊红染色,分析根管内矿化组织和软组织形成。用 Masson 三色和苦味酸天狼猩红染色评估胶原的存在和成熟情况。进行增殖细胞核抗原(PCNA)和骨钙素(OCN)的免疫标记分析。数据采用曼-惠特尼 U 检验(p<0.05)。
REP-SS 和 REP-F18Co 组矿化组织厚度和长度相似(p>0.05)。关于新形成的软组织的存在,REP-F18Co 的大多数标本在根管的颈三分之一处有组织形成,而 REP-SS 的标本在根管的中三分之一处有组织形成(p<0.05),并且 REP-F18Co 中的胶原成熟度更高(p<0.05)。根尖三分之一处的 PCNA 阳性细胞数量在 F18Co 组显著增加,OCN 免疫标记在大多数 REP-F18Co 标本中严重,在大多数 REP-SS 标本中较低。
REP 中最后用 F18Co 生物活性玻璃溶液冲洗不会影响矿化组织的形成,但会诱导根管内软组织形成,胶原成熟度增加,PCNA 阳性细胞和 OCN 免疫标记增加。