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首页> 外文期刊>Clinical oral investigations >Proliferation of rat molar pulp cells after direct pulp capping with dentine adhesive and calcium hydroxide.
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Proliferation of rat molar pulp cells after direct pulp capping with dentine adhesive and calcium hydroxide.

机译:用牙本质粘合剂和氢氧化钙直接覆盖牙髓后,大鼠磨牙牙髓细胞的增殖。

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The aim was to evaluate the proliferation of pulp cells 1, 3 and 7 days after direct pulp capping with the dentine adhesive Gluma Comfort Bond (GCB) and to compare it with calcium hydroxide (Ca(OH)(2)). An occlusal cavity was prepared in 72 molar teeth of 36 Wistar rats. Then GCB or Ca(OH)(2) was placed on the exposed pulp. All cavities were restored with composite. After 1, 3 and 7 days, the animals were sacrificed. One hour prior sacrification, 5-bromo-2'-desoxyuridine (BrdU) was injected into the intraperitoneal cavity for immunohistological analysis of 18 animals. BrdU was incorporated into the DNA to tag proliferating cells using an antibody staining. Three animals served as controls and were not further treated. The number of the tagged cells was statistically analysed by comparing the results of the three groups. In 18 rats, routine histological analysis was performed in order to evaluate the pulp tissue for bacterial infection, inflammatory cells and necrosis. The marked cells were identified as fibroblasts, endothelial cells (after 1, 3 and 7 days) and Hohl cells (after 7 days). One day after capping, significantly more cells were stained in the GCB than in the Ca(OH)(2) group (p < 0.05). After 3 days, significantly more cells were stained in the GCB than in the Ca(OH)(2) and the control group (p < 0.016). Direct contact of GCB with pulp tissue leads to an increased formation of granulation tissue (fibroblasts, endothelial cells) because of an inflammatory reaction. This may be explained by missing antibacterial effect and foreign body reactions. Also, GCB may have a negative effect on Hohl cells.
机译:目的是评估在用牙本质粘合剂Gluma Comfort Bond(GCB)直接覆盖牙髓后1、3和7天,牙髓细胞的增殖,并将其与氢氧化钙(Ca(OH)(2))进行比较。在36只Wistar大鼠的72颗磨牙中制备了咬合腔。然后将GCB或Ca(OH)(2)放在裸露的纸浆上。用复合材料修复所有型腔。在1、3和7天后,处死动物。处死前一小时,将5-溴-2'-脱氧尿苷(BrdU)注入腹腔内,对18只动物进行免疫组织学分析。使用抗体染色将BrdU掺入DNA以标记增殖细胞。三只动物作为对照,不作进一步处理。通过比较三组的结果,统计分析标记细胞的数量。在18只大鼠中,进行了常规组织学分析,以评估牙髓组织的细菌感染,炎性细胞和坏死情况。标记的细胞被鉴定为成纤维细胞,内皮细胞(1、3和7天后)和Hohl细胞(7天后)。封盖后一天,GCB中的细胞染色明显多于Ca(OH)(2)组(p <0.05)。 3天后,GCB中的细胞染色明显多于Ca(OH)(2)和对照组(p <0.016)。由于炎症反应,GCB与牙髓组织直接接触会导致肉芽组织(成纤维细胞,内皮细胞)形成增加。这可能是由于缺少抗菌作用和异物反应造成的。同样,GCB可能对Hohl细胞产生负面影响。

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