Eber R M, Shuler C F, Buchanan W, Beck F M, Horton J E
Section of Diagnostic Services, Ohio State University College of Dentistry, Columbus.
J Periodontol. 1989 Aug;60(8):429-34. doi: 10.1902/jop.1989.60.8.429.
In vitro cytotoxicity studies of periodontal dressings have not generally produced a result consistent with in vivo observations. These prior in vitro studies have not used human intraoral cell lines. We tested the effects of two eugenol containing and two non-eugenol periodontal dressings on cultured human gingival fibroblasts (HGF) (ATCC #1292). Replicate HGF cultures grown in microtiter plates were exposed to stock, 1:4 and 1:16 dilutions of extracts made from each of the four periodontal dressings. The HGF cultures were pulse labelled with tritiated thymidine (3HTdR) after 24, 48, and 72 hours. Incorporations of the labelled thymidine were measured using liquid scintillation counting and expressed as counts per minute. The results showed that undiluted extracts from all four periodontal dressings totally inhibited 3HTdR uptake (P less than 0.05). The 1:4 dilution of eugenol dressings inhibited 3HTdR uptake significantly more than non-eugenol dressings (P less than 0.05). Interestingly, at 72 hours the 1:16 dilution of the non-eugenol dressings caused significantly increased 3HTdR uptake which was not observed with the eugenol dressings. The present results suggest that the use of a human fibroblastic cell line for testing the effects of periodontal dressings may provide information about the relative biological effects of these dressings. Using this cell line, we have found that eugenol dressings inhibit fibroblast proliferation to a greater extent than non-eugenol dressings.
牙周敷料的体外细胞毒性研究结果通常与体内观察结果不一致。这些先前的体外研究未使用人口腔内细胞系。我们测试了两种含丁香酚和两种不含丁香酚的牙周敷料对培养的人牙龈成纤维细胞(HGF)(ATCC #1292)的影响。在微量滴定板中生长的重复HGF培养物暴露于由四种牙周敷料中的每一种制成的提取物的原液、1:4和1:16稀释液。在24、48和72小时后,用氚标记的胸腺嘧啶核苷(3HTdR)对HGF培养物进行脉冲标记。使用液体闪烁计数法测量标记胸腺嘧啶核苷的掺入量,并以每分钟计数表示。结果表明,所有四种牙周敷料的未稀释提取物完全抑制了3HTdR摄取(P小于0.05)。丁香酚敷料的1:4稀释液对3HTdR摄取的抑制作用明显大于非丁香酚敷料(P小于0.05)。有趣的是,在72小时时,非丁香酚敷料的1:16稀释液导致3HTdR摄取显著增加,而丁香酚敷料未观察到这种情况。目前的结果表明,使用人成纤维细胞系来测试牙周敷料的效果可能会提供有关这些敷料相对生物学效应的信息。使用这种细胞系,我们发现丁香酚敷料比非丁香酚敷料更能抑制成纤维细胞增殖。