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牙科高速涡轮钻对培养细胞影响的实验研究(体外)(作者译)

[An experimental study of the effects of drilling with dental high speed turbine on culture cells (in vitro) (author's transl)].

作者信息

Ohta M

出版信息

Shika Rikogaku Zasshi. 1976 May;17(38):102-11.

PMID:784883
Abstract

A drilling at 500 000 R.P.M. with a dental high speed turbine was made either to a tissue culture bottle or to a test tube, in which mouse L fibroblasts were grown for 2 days with YLH medium supplemented with 10% bovine serum, in order to examine the effects of high speed drilling to the cells in vitro, Experiments were carried out with the following three conditions; (1) Drilling of outer surface of the glasswares at the inner surface on which the cells were attached, with a water coolant, (2) Drilling of the same place without a water coolant, and (3) Drilling of a remote area of the glasswares where no cells were grown. The last experimental condition permitted to give a sole effect of vibration accompanied with the drilling. Rates of cell multiplication and morphological observation were obtained on 2 days and 5 days after the glasswares were drilled. Rates of cell multiplication showed no change between the experimental conditions and control. This means that heat generation, vibration and/or their compound effects during drilling did not deter cells from growing. Morphological change of the cells due to the drilling was parallel to the results of cell multiplication except the drilling without a water coolant. When drilled without a water coolant, the cells around the drilled area was deteriorated and died after 24 hours. However, most of the cells away from the drilled area were not affected. The present results can not directly apply to the drilling in dental clinic, since in vivo condition has more complicated situation, some of which can not be simulated in in vitro environment. However, the in vitro results can surely be important information in resolving drilling effects in vivo.

摘要

使用牙科高速涡轮机以500000转/分钟的转速对装有小鼠L成纤维细胞并添加10%牛血清的YLH培养基培养2天的组织培养瓶或试管进行钻孔,以研究高速钻孔对体外细胞的影响。实验在以下三种条件下进行:(1)在细胞附着的玻璃器皿内表面使用水冷对其外表面进行钻孔;(2)在相同位置不使用水冷进行钻孔;(3)在玻璃器皿中没有细胞生长的偏远区域进行钻孔。最后一种实验条件仅能产生钻孔时伴随的振动影响。在玻璃器皿钻孔后的第2天和第5天获得细胞增殖率和形态观察结果。实验条件与对照组之间的细胞增殖率没有变化。这意味着钻孔过程中的发热、振动和/或它们的复合效应不会阻碍细胞生长。除了不使用水冷钻孔的情况外,钻孔导致的细胞形态变化与细胞增殖结果一致。不使用水冷钻孔时,钻孔区域周围的细胞在24小时后恶化并死亡。然而,远离钻孔区域的大多数细胞未受影响。目前的结果不能直接应用于牙科临床钻孔,因为体内情况更为复杂,其中一些无法在体外环境中模拟。然而,体外结果肯定是解决体内钻孔影响的重要信息。

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