Department of Conservative Dentistry, Medical University of Vienna, Vienna, Austria.
Int Endod J. 2011 Jan;44(1):33-40. doi: 10.1111/j.1365-2591.2010.01792.x. Epub 2010 Aug 31.
To investigate whether zoledronate (ZOL) can cause a cytotoxic response in dental pulp-derived cells (DPCs) in vitro.
Cell activity was assessed utilizing MTT tests, (3) [H]thymidine, and (3) [H]leucine incorporation assays in human DPCs in response to ZOL. Cell activity assays were also preformed on calcium phosphate-coated plates. Cell death was analysed with annexin V/propidium iodide, trypan blue staining and Western blot analysis.
Micromolar concentrations of ZOL were required to decrease the activity of DPCs. The decreased activity of DPCs was associated with the occurrence of apoptosis and necrosis. No adverse effects were observed when DPCs were cultured on calcium phosphate-coated plates with ZOL.
High concentrations of soluble ZOL were required to cause adverse effects in vitro. These adverse effects are abolished when the bisphosphonate was bound to a mineralized surface. However, the clinical relevance of these results remains to be determined.
研究唑来膦酸(zoledronate,ZOL)在体外是否会对牙髓细胞(dental pulp-derived cells,DPCs)产生细胞毒性反应。
采用 MTT 试验、(3)[H]胸苷掺入试验和(3)[H]亮氨酸掺入试验,检测 ZOL 对人牙髓细胞活力的影响。在钙磷涂层板上进行细胞活力检测。采用 Annexin V/碘化丙啶、台盼蓝染色和 Western blot 分析检测细胞死亡情况。
只有在微摩尔浓度的 ZOL 作用下,才能降低 DPCs 的活性。DPCs 活性的降低与细胞凋亡和坏死的发生有关。当 DPCs 在钙磷涂层板上培养时,ZOL 无不良影响。
可溶性 ZOL 需达到高浓度才能在体外产生不良反应。当双膦酸盐与矿化表面结合时,这些不良反应会被消除。然而,这些结果的临床相关性仍有待确定。