Gundogan Gul Ipek, Durmus Sare, Ozturk Gulgun Cansu, Kucukyesil Nazmi, Acar Yasin Talat, Balaban Rumeysa, Kig Cenk
Department of Histology and Embryology, Faculty of Medicine, Istanbul Yeni Yuzyil University, Istanbul, Turkey.
Department of Endodontics, Faculty of Dentistry, Istanbul Yeni Yuzyil University, Istanbul, Turkey.
Aust Endod J. 2021 Dec;47(3):569-579. doi: 10.1111/aej.12541. Epub 2021 Jul 18.
We aimed to investigate the in vitro physiologic effects of xylene, chloroform, orange oil and eucalyptus oil solvents for dissolving gutta-percha on L929 and HOB cell lines; 2.5 and 10 μL mL of these solvents were tested for 24, 48 and 72 h. Gutta-percha solvents inhibited the proliferation rate of fibroblasts in a dose- and time-dependent manner; however, no inhibition was detected in HOB (evaluated using MTT assay). None of the solvents induced apoptosis/necrosis in HOB cells at ≤2.5 μL mL concentration in contrast to L929 (determined using acridine orange/ethidium bromide dual staining). Each solvent tested reduced the migration rate of both L929 and HOB cell lines in a dose-dependent manner (evaluated using a scratch assay). Gutta-percha solvents can damage fibroblast-rich tissues. Osteoblasts seemed to be more resistant to the tested solvents, and excessive extrusion of solvents from the root canal may also damage the periradicular tissues and reduce the ability to repair.
我们旨在研究用于溶解牙胶的二甲苯、氯仿、橙油和桉叶油溶剂对L929和HOB细胞系的体外生理作用;测试了2.5和10 μL/mL的这些溶剂作用24、48和72小时的情况。牙胶溶剂以剂量和时间依赖性方式抑制成纤维细胞的增殖率;然而,在HOB细胞中未检测到抑制作用(使用MTT法评估)。与L929细胞相反(使用吖啶橙/溴化乙锭双重染色测定),在浓度≤2.5 μL/mL时,没有一种溶剂诱导HOB细胞凋亡/坏死。所测试的每种溶剂均以剂量依赖性方式降低L929和HOB细胞系的迁移率(使用划痕试验评估)。牙胶溶剂可损害富含成纤维细胞的组织。成骨细胞似乎对所测试的溶剂更具抗性,并且根管内溶剂的过度挤出也可能损害根尖周组织并降低修复能力。