Willershausen B, Hagedorn B, Tekyatan H, Briseño Marroquín B
Department for Operative Dentistry, Johannes Gutenberg University-Mainz, Germany.
Eur J Med Res. 2004 Jul 30;9(7):345-50.
The aim of the present study was to demonstrate the possible effect of different endodontic calcium hydroxide and chlorhexidine-based gutta-percha points, on two different human cell culture systems. Two different calcium hydroxide (Roeko, Langenau, Germany) and one chlorhexidine (Activ Point/Roeko, Langenau, Germany) gutta-percha points were tested with gingival fibroblasts and epithelial tumor cells over a period of six days (n = 12). Conventional gutta-percha points (VDW, Munich, Germany) and cells that were not exposed to any substances served as controls (n = 12). Study parameters included cell vitality, cell count, protein synthesis and cell proliferation.
All tested materials induced cell growth specific alterations. Chlorhexidine-based gutta-percha points showed a significant lower protein synthesis with both, gingival fibroblasts (0.013 +/- 0.009 mg/ml) and epithelial tumor cells (0.07 +/- 0.039 mg/ml), when compared with the controls (p > 0.05). Protein synthesis increase of the epithelial tumor cells (0.581 +/- 0.013 mg/ml, control) was observed with the conventional gutta-percha points (0.688 +/- 0.078 mg/ml) and with both gutta-percha points containing different calcium hydroxide-based formulations (0.776 +/- 0.115 and 0.7 +/- 0.047 mg/ ml).
Under the conditions of this study, chlorhexidine containing gutta-percha points showed the highest effect on cell growth inhibition. No significant differences were observed between the tested material and the two different cell culture types.
本研究的目的是证明不同的牙髓用氢氧化钙和氯己定类牙胶尖对两种不同的人类细胞培养系统可能产生的影响。两种不同的氢氧化钙(德国朗根瑙的罗伊科公司生产)和一种氯己定(德国朗根瑙的罗伊科公司生产的活性牙胶尖)牙胶尖在六天时间内对牙龈成纤维细胞和上皮肿瘤细胞进行了测试(n = 12)。传统牙胶尖(德国慕尼黑的VDW公司生产)和未接触任何物质的细胞作为对照(n = 12)。研究参数包括细胞活力、细胞计数、蛋白质合成和细胞增殖。
所有测试材料均引起细胞生长的特定改变。与对照组相比,氯己定类牙胶尖在牙龈成纤维细胞(0.013±0.009毫克/毫升)和上皮肿瘤细胞(0.07±0.039毫克/毫升)中均显示出显著较低的蛋白质合成(p>0.05)。传统牙胶尖(0.688±0.078毫克/毫升)以及两种含不同氢氧化钙配方的牙胶尖(0.776±0.115和0.7±0.047毫克/毫升)可使上皮肿瘤细胞(对照为0.581±0.013毫克/毫升)的蛋白质合成增加。
在本研究条件下,含氯己定的牙胶尖对细胞生长抑制作用最强。在测试材料和两种不同细胞培养类型之间未观察到显著差异。