Daunorubicin-induced pathology in the developing hamster molar tooth germ in vitro.

D M Lyaruu, M A van Duin, T J Bervoets, A L Bronckers, J H Wöltgens
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引用次数: 12

Abstract

The aim of this study was to evaluate, under organ culture conditions, the cytotoxic effects of daunorubicin on tooth development. Three-day-old maxillary hamster second molars were exposed for 24 h in vitro to 108-10-4 M daunorubicin and then evaluated biochemically and histologically. At 10-6 M daunorubicin dose-dependently decreased tooth germ dry weight, cell proliferation ([3H]thymidine uptake), and insoluble [32P] phosphate uptake (phosphorylation of macromolecules). [45Ca]calcium uptake, a marker for mineralization, was significantly affected only at the highest concentration (10-4 M) tested. Histologically, 10-6 M daunorubicin induced necrosis of the proliferating but not the differentiated protein-secreting cells. At 10-4 M, however, all cells were dead. These results indicate that daunorubicin is particularly toxic to the proliferating cells of the tooth germ. Thus, it can be postulated that children treated with daunorubicin may develop defects in the erupted teeth mainly associated with those regions that were in the proliferating stage at the onset of anticancer chemotherapy.

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柔红霉素诱导发育中的仓鼠磨牙胚的体外病理。
本研究的目的是评估在器官培养条件下,柔红霉素对牙齿发育的细胞毒性作用。采用108-10-4 M柔红霉素体外培养3日龄上颌地鼠第二磨牙24 h,进行生化和组织学评价。在10-6 M时,柔红霉素剂量依赖性地降低了牙胚干重、细胞增殖([3H]胸苷摄取)和不溶性[32P]磷酸盐摄取(大分子磷酸化)。[45Ca]钙吸收是矿化的标志,仅在最高浓度(10-4 M)测试时才受到显著影响。组织学上,10-6 M柔红霉素诱导增殖细胞坏死,但未诱导分化的蛋白分泌细胞坏死。10-4 M时,细胞全部死亡。这些结果表明柔红霉素对牙齿胚芽的增殖细胞具有特别的毒性。因此,可以推测,接受柔红霉素治疗的儿童可能在萌出的牙齿中出现缺陷,主要与抗癌化疗开始时处于增殖阶段的那些区域有关。
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