Department of Pediatric Dentistry, School of Dentistry of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Faculty of Amazonas, Manaus, Amazonas, Brazil.
Int Endod J. 2019 Oct;52(10):1489-1500. doi: 10.1111/iej.13145. Epub 2019 Jun 5.
To evaluate in vivo tissue responses after sealing furcation perforations in dog's teeth with either Biodentine™, mineral trioxide aggregate (MTA) or gutta-percha, by means of histopathological, histoenzymological, immunohistochemical and immunofluorescence analysis.
After root canal treatment, perforations were created in the central region of the pulp chamber floor using a round diamond bur and filled with one or other of the materials. The animals were euthanized after 120 days, and the teeth (n = 30) were processed for histopathological analysis of new mineralized tissue formation and collagen fibre reinsertion, immunohistochemical analysis of osteopontin (OPN) and alkaline phosphatase (ALP) and immunofluorescence analysis for bone morphogenetic protein (BMP-2), cementum attachment protein (CAP), bone sialoprotein (BSP), osteocalcin (OCN) and cementum protein1 (CEMP1). Histoenzymology was performed for TRAP activity and osteoclast count. Data were analysed statistically (α = 0.05) using chi-square and Kruskal-Wallis tests.
Gutta-percha did not induce mineralized tissue formation. MTA and Biodentine formed mineralized tissue in 88% and 92% of specimens, respectively, with no significant difference (P > 0.05). Gutta-percha was associated with scattered collagen fibres parallel to the perforations. Groups treated with MTA or Biodentine had partial fibre reinsertion perpendicular to the newly formed mineralized tissue. All materials induced OPN and ALP expression, weakest for gutta-percha and strongest for MTA (P < 0.05). Only MTA induced BMP-2, BSP, OCN, CAP and CEMP1 expression. Osteoclast counts were similar in all groups (P = 0.97).
Mineral trioxide aggregate and Biodentine were biocompatible, with formation of mineralized tissue and partial reinsertion of collagen fibres. In addition, the participation of several molecules by which calcium silicate-based materials induce the formation of mineralized tissue were noted, with expression of ALP and OPN mineralization markers, without interference in the number of osteoclasts. Only MTA stimulated the expression of proteins associated with the formation of a cementum-like mineralized tissue.
通过组织病理学、组织化学、免疫组织化学和免疫荧光分析,评估用 BiodentineTM、三氧化矿物聚合体(MTA)或牙胶封闭狗牙分叉穿孔后的体内组织反应。
在根管治疗后,使用圆形钻石车针在牙髓室底的中央区域制造穿孔,并填充一种或另一种材料。动物在 120 天后被安乐死,将 30 颗牙齿(n=30)进行处理,用于新矿化组织形成和胶原纤维再插入的组织病理学分析、骨桥蛋白(OPN)和碱性磷酸酶(ALP)的免疫组织化学分析以及骨形态发生蛋白(BMP-2)、牙骨质附着蛋白(CAP)、骨唾液蛋白(BSP)、骨钙素(OCN)和牙骨质蛋白 1(CEMP1)的免疫荧光分析。进行组织化学分析以检测 TRAP 活性和破骨细胞计数。使用卡方检验和 Kruskal-Wallis 检验对数据进行统计学分析(α=0.05)。
牙胶未诱导矿化组织形成。MTA 和 Biodentine 分别在 88%和 92%的标本中形成矿化组织,无显著差异(P>0.05)。牙胶与平行于穿孔的散在胶原纤维有关。用 MTA 或 Biodentine 治疗的组有部分纤维沿新形成的矿化组织垂直再插入。所有材料均诱导 OPN 和 ALP 表达,牙胶最弱,MTA 最强(P<0.05)。仅 MTA 诱导 BMP-2、BSP、OCN、CAP 和 CEMP1 表达。所有组的破骨细胞计数相似(P=0.97)。
三氧化矿物聚合体和 Biodentine 具有生物相容性,可形成矿化组织并部分再插入胶原纤维。此外,还观察到几种钙硅酸钠基材料诱导矿化组织形成的分子参与,表达 ALP 和 OPN 矿化标志物,而不干扰破骨细胞数量。只有 MTA 刺激与形成类牙骨质矿化组织相关的蛋白质的表达。