体外培养第12.5天和第13.5天胎鼠腭对5 -氟尿嘧啶和羟基脲的敏感性

T. Kosazuma, S. Kawauchi, M. Chou, K. Shiota
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引用次数: 8

摘要

采用悬浮培养技术,将第12.5天和第13.5天ICR小鼠胎儿的上颌区培养在化学定义的无血清培养基中,以检测5 -氟尿嘧啶(5 - FU)和羟基脲(HU)对培养的腭的毒性作用,并比较不同发育阶段胎儿小鼠腭的敏感性。将第12.5天和第13.5天的胎鼠的腭部外植,并在体外暴露于0.1-50 μg 5 - FU/ml或5 - 76 μg HU/ml中72小时。5‐FU在体外对龄12.5天的腭架生长和融合的抑制作用依赖于其浓度。第13.5天的胎儿腭部对5‐FU的敏感性明显低于第12.5天,第12.5天和第13.5天的胎儿腭部5‐FU的最小毒性浓度(mtc)分别为0.1和10 μg/ml。HU以浓度依赖性的方式抑制第12.5天胎儿腭架的体外生长和融合,但仅轻微抑制第13.5天胎儿腭架的生长。在第12.5天和第13.5天的胎儿腭中,HU的MTCs分别为19和76 μg/ml。因此,第12.5天的小鼠胎儿腭(在发育的第1阶段或早期阶段)似乎比第13.5天的小鼠胎儿腭(在发育的第2-3阶段)更容易受到这些致畸化学物质的影响。第12.5天ICR胎鼠的腭可能比第13.5天的腭更适合体外致畸原筛选和正常和异常腭发生机制的研究。
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Susceptibility of Day‐12.5 and Day‐13.5 Fetal Mouse Palates Cultured in Vitro to 5‐Fluorouracil and Hydroxyurea
Abstract The maxillary regions of day‐12.5 and day‐13.5 ICR mouse fetuses were cultivated in a chemically‐defined serumless medium by a suspension culture technique to examine the toxic effects of 5‐fluorouracil (5‐FU) and hydroxyurea (HU) on cultured palates and to compare the sensitivity of fetal mouse palates at different stages of development. The palates of day‐12.5 and day‐13.5 fetal mice were explanted and exposed in vitro for 72 hr to 0.1–50 μg 5‐FU/ml or to 5–76 μg HU/ml. 5‐FU inhibited the growth and fusion of day‐12.5 palatal shelves in vitro dependently on its concentrations. Day‐13.5 palates were significantly less sensitive to 5‐FU than day‐12.5 palates, and the minimal toxic concentrations (MTCs) of 5‐FU were 0.1 and 10 μg/ml for day‐12.5 and day‐13.5 fetal palates, respectively. HU inhibited the in vitro growth and fusion of day‐12.5 fetal palatal shelves in a concentration dependent manner, but only slightly suppressed the growth of day‐13.5 fetal palates. The MTCs of HU were 19 and 76 μg/ml for day‐12.5 and day‐13.5 fetal palates, respectively. Therefore, day‐12.5 fetal mouse palates (at stage‐1 or earlier stages of palatogenesis) seemed significantly more susceptible to these teratogenic chemicals than day‐13.5 fetal palates (at stages 2–3 of palatogenesis). The palates of day‐12.5 ICR fetal mice may be more suitable than day‐13.5 palates for in vitro teratogen screening and for the study of mechanisms of normal and abnormal palatogenesis.
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