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通过姐妹染色单体交换评估氟化物的遗传毒性作用。

Genotoxic effects of fluoride evaluated by sister-chromatid exchange.

作者信息

Li Y M, Heerema N A, Dunipace A J, Stookey G K

机构信息

Oral Health Research Institute, Indiana University School of Dentistry, Indianapolis 46202.

出版信息

Mutat Res. 1987 Nov;192(3):191-201. doi: 10.1016/0165-7992(87)90055-8.

Abstract

The purpose of this investigation was to study the genotoxic potential of fluoride (in the form of sodium fluoride, NaF) using in vitro and in vivo sister-chromatid exchange (SCE) assays with Chinese hamster cells. The NaF concentrations used in cultures of Chinese hamster ovary (CHO) cells ranged from 0 to 6.3 mM, both with and without S9 activation. Fluoride analysis of the culture medium demonstrated that it contained little indigenous fluoride, and the concentration of added fluoride was not affected by the components of the medium or the S9 mix. The CHO cells cultured in 6.3 mM NaF almost vanished, and at the concentration of 5.3 mM NaF in cultures without S9 microsome, only M1 cells were observed. In in vivo studies, Chinese hamsters were intubated with NaF dosages of 0, 0.1, 1.0, 10, 60 and 130 mg/kg, and the bone marrow (CHBM) cells were examined for SCE frequencies. Bone fluoride data showed that the intubated NaF was effectively absorbed. Death occurred in 3 of the 8 animals given 130 mg NaF/kg. The results indicated that NaF, in dosages up to 5.3 mM in CHO cell cultures and 130 mg/kg in in vivo CHBM cells, did not significantly increase the SCE frequencies over those observed in the negative (distilled water) controls. However, examination of the cell cycle revealed an inhibitory effect of NaF on cell proliferation with doses of NaF at or greater than 1.0 mM in cultured CHO cells and at or greater than 60 mg NaF/kg in in vivo CHMB cells. The results of the present study indicated an inhibition of the cell cycle and death of the cells with increasing concentrations of fluoride but not effect of fluoride on SCE frequency in CHO and CHBM cells.

摘要

本研究的目的是使用中国仓鼠细胞的体外和体内姐妹染色单体交换(SCE)试验,研究氟化物(以氟化钠,NaF形式)的遗传毒性潜力。中国仓鼠卵巢(CHO)细胞培养物中使用的NaF浓度范围为0至6.3 mM,有和没有S9活化。培养基的氟化物分析表明,其含有的内源性氟化物很少,添加的氟化物浓度不受培养基成分或S9混合物的影响。在6.3 mM NaF中培养的CHO细胞几乎消失,在没有S9微粒体的培养物中,NaF浓度为5.3 mM时,仅观察到M1细胞。在体内研究中,给中国仓鼠插管给予0、0.1、1.0、10、60和130 mg/kg的NaF剂量,并检查骨髓(CHBM)细胞的SCE频率。骨氟数据表明,插管给予的NaF被有效吸收。给予130 mg NaF/kg的8只动物中有3只死亡。结果表明,在CHO细胞培养物中剂量高达5.3 mM以及在体内CHBM细胞中剂量高达130 mg/kg时,NaF不会比阴性(蒸馏水)对照中观察到的SCE频率显著增加。然而,细胞周期检查显示,在培养的CHO细胞中,NaF剂量为1.0 mM或更高时,以及在体内CHMB细胞中,NaF剂量为60 mg/kg或更高时,NaF对细胞增殖有抑制作用。本研究结果表明,随着氟化物浓度增加,细胞周期受到抑制且细胞死亡,但氟化物对CHO和CHBM细胞的SCE频率没有影响。

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